Subcellular Location: Membrane

Found 500 associated metabolites.

5805 associated genes.

A4GALT, A4GNT, AAAS, AADAC, AADACL2, AADACL3, AADACL4, AARS1, AATK, ABCA1, ABCA10, ABCA12, ABCA13, ABCA2, ABCA3, ABCA4, ABCA5, ABCA6, ABCA7, ABCA8, ABCA9, ABCB1, ABCB11, ABCB4, ABCB5, ABCB6, ABCB7, ABCB8, ABCB9, ABCC1, ABCC10, ABCC12, ABCC2, ABCC3, ABCC4, ABCC5, ABCC6, ABCC8, ABCC9, ABCD1, ABCD3, ABCD4, ABCE1, ABCF1, ABCF2, ABCF3, ABCG1, ABCG2, ABCG4, ABCG5, ABCG8, ABHD1, ABHD12, ABHD13, ABHD14A, ABHD15, ABHD16A, ABHD17A, ABHD17B, ABHD2, ABHD3, ABHD6, ABI3, ABO, ABR, ABTB3, ACAA1, ACAP1, ACAP2, ACAT1, ACBD3, ACBD4, ACBD5, ACE, ACE2, ACER3, ACHE, ACKR1, ACLY, ACMSD, ACOX1, ACOX3, ACP2, ACP4, ACP5, ACSBG2, ACSL1, ACSL3, ACSL4, ACSL5, ACSL6, ACSM1, ACSM2B, ACTB, ACTBL2, ACTC1, ACTG1, ACTL9, ACTR1B, ACTR2, ACTR3, ACVR1, ACVR1B, ACVR1C, ACVR2B, ACVRL1, ADA, ADAM10, ADAM11, ADAM12, ADAM17, ADAM18, ADAM19, ADAM2, ADAM20, ADAM22, ADAM23, ADAM28, ADAM30, ADAM32, ADAM33, ADAM7, ADAM8, ADAM9, ADAMTS4, ADAR, ADCK2, ADCK5, ADCY1, ADCY2, ADCY3, ADCY4, ADCY5, ADCY6, ADCY7, ADCY8, ADCY9, ADCYAP1R1, ADD3, ADGRA1, ADGRA2, ADGRA3, ADGRB1, ADGRB2, ADGRB3, ADGRD1, ADGRD2, ADGRE2, ADGRE3, ADGRE4P, ADGRE5, ADGRF1, ADGRF2, ADGRF3, ADGRF4, ADGRF5, ADGRG1, ADGRG2, ADGRG3, ADGRG4, ADGRG5, ADGRG6, ADGRG7, ADGRL1, ADGRL2, ADGRL3, ADGRL4, ADGRV1, ADIG, ADIPOR1, ADORA2A, ADORA2B, ADPGK, ADPRM, ADRA1B, ADRB2, ADSS1, ADTRP, AFG3L2, AGAP2, AGER, AGFG2, AGMO, AGO2, AGO3, AGO4, AGPAT1, AGPAT2, AGPAT3, AGPAT4, AGPAT5, AGPS, AGRN, AGTR1, AHNAK, AIDA, AIFM1, AIG1, AIMP1, AIMP2, AIP, AK6, AKAP1, AKAP10, AKAP12, AKAP13, AKAP5, AKAP8, AKIRIN2, AKNA, AKT1, AKT3, ALDH16A1, ALDH3A2, ALDOA, ALG1, ALG10, ALG11, ALG12, ALG2, ALG3, ALG5, ALG6, ALG9, ALK, ALOX12, ALOX15, ALOX15B, ALOX5AP, ALPL, ALYREF, AMER3, AMFR, AMHR2, AMIGO1, AMIGO2, AMIGO3, AMN, AMOT, ANK1, ANK2, ANK3, ANKAR, ANKFY1, ANKH, ANKLE1, ANKLE2, ANKRA2, ANKRD17, ANKRD27, ANKRD29, ANKRD46, ANKZF1, ANO1, ANO10, ANO2, ANO3, ANO4, ANO5, ANO6, ANO7, ANO8, ANTXR1, ANTXR2, ANTXRL, ANXA1, ANXA11, ANXA13, ANXA2, ANXA3, ANXA4, ANXA5, ANXA6, ANXA7, AOC3, AP1G1, AP1G2, AP1M1, AP1S1, AP2A1, AP2B1, AP3B1, AP3D1, AP4E1, AP4S1, AP5M1, APAF1, APBB2, APBB3, APCDD1L, APH1A, APH1B, API5, APLP1, APLP2, APMAP, APOBR, APOE, APOL1, APOL2, APOL3, APOL4, APOL6, APOLD1, APP, APPBP2, APPL1, APPL2, APRG1, AQP1, AQP12A, AQP12B, AQP2, AQP3, AQP4, AQP6, AQP7, AQP7B, AQP8, AQP9, AQR, AR, ARB2BP, ARC, ARCN1, AREG, AREL1, ARF4, ARF5, ARF6, ARFGAP1, ARFGAP2, ARFGAP3, ARFGEF2, ARFRP1, ARHGAP1, ARHGAP15, ARHGAP21, ARHGAP26, ARHGAP27, ARHGAP32, ARHGAP42, ARHGAP45, ARHGDIA, ARHGDIB, ARHGDIG, ARHGEF1, ARHGEF11, ARHGEF12, ARIH2OS, ARL1, ARL10, ARL6, ARL6IP1, ARL6IP5, ARL6IP6, ARL8A, ARL8B, ARMC10, ARMC5, ARMCX2, ARMCX3, ARMCX4, ARMH4, ARPC3, ARSH, ARSJ, ARSK, ARSL, ART3, ART4, ASAH1, ASAP1, ASB11, ASB18, ASB5, ASCC3, ASGR1, ASGR2, ASIC1, ASIC3, ASIC4, ASIC5, ASPHD1, ASPHD2, ASPRV1, ASTN1, ASTN2, ATAD1, ATAD3A, ATCAY, ATF6, ATG5, ATG9A, ATIC, ATL1, ATL2, ATL3, ATP10A, ATP10B, ATP10D, ATP11A, ATP11B, ATP11C, ATP13A1, ATP13A2, ATP13A3, ATP13A4, ATP13A5, ATP1A1, ATP1A2, ATP1A3, ATP1A4, ATP1B1, ATP1B2, ATP1B3, ATP1B4, ATP2A1, ATP2A2, ATP2A3, ATP2B1, ATP2B2, ATP2B3, ATP2B4, ATP2C1, ATP2C2, ATP4A, ATP5F1A, ATP5F1B, ATP5F1C, ATP5MC1, ATP5MG, ATP5MJ, ATP5PB, ATP5PO, ATP6AP1, ATP6AP1L, ATP6AP2, ATP6V0A1, ATP6V0A2, ATP6V0A4, ATP6V0B, ATP6V0C, ATP6V0D1, ATP6V0D2, ATP6V0E1, ATP6V0E2, ATP6V1A, ATP6V1D, ATP6V1F, ATP6V1H, ATP7A, ATP7B, ATP8A1, ATP8A2, ATP8B1, ATP8B2, ATP8B3, ATP8B4, ATP9A, ATP9B, ATPSCKMT, ATRNL1, ATXN10, ATXN2, ATXN2L, AUP1, AVEN, AVL9, AVPR2, AXIN1, AXL, AZIN2, AZU1, B2M, B3GALNT1, B3GALT1, B3GALT6, B3GALT9, B3GAT1, B3GAT2, B3GAT3, B3GNT5, B3GNT6, B4GALNT1, B4GALNT2, B4GALT1, B4GALT2, B4GALT4, B4GALT7, B9D1, B9D2, BACE1, BACE2, BAG1, BAG3, BAG4, BAG5, BAG6, BAIAP2, BAK1, BAMBI, BAX, BBS2, BBS7, BBS9, BCAM, BCAP29, BCAP31, BCAR1, BCAR3, BCAR4, BCL2, BCL2L10, BCL2L12, BCL2L13, BCL2L14, BCL2L2, BCL2L2-PABPN1, BCR, BCS1L, BDH1, BDNF, BEAN1, BEGAIN, BEST1, BEST2, BEST3, BET1, BET1L, BFAR, BICD1, BID, BIN1, BIRC6, BLCAP, BLNK, BLOC1S6, BLTP1, BMPR1A, BMPR1B, BNIP1, BNIP3, BNIP3L, BOK, BORCS5, BORCS7-ASMT, BPI, BPNT2, BRAT1, BRCA1, BRCA2, BRI3BP, BRICD5, BRS3, BSCL2, BSG, BSPRY, BST1, BST2, BTC, BTF3, BTN1A1, BTN2A1, BTN2A2, BTN2A3P, BTN3A1, BTN3A2, BTN3A3, BTNL10P, BTNL2, BTNL3, BTNL8, BTNL9, BUB1, BVES, BYSL, BZW1, BZW2, C10orf105, C11orf87, C12orf76, C14orf132, C15orf48, C16orf54, C16orf89, C16orf92, C17orf78, C18orf15, C19orf18, C19orf38, C1GALT1, C1GALT1C1, C1GALT1C1L, C1orf115, C1orf159, C1orf162, C1orf185, C1orf210, C1orf43, C1QB, C1QBP, C1QTNF3, C1QTNF6, C20orf141, C20orf173, C2CD2, C2orf74, C2orf92, C3orf18, C3orf20, C3orf33, C3orf80, C5orf15, C5orf60, C6orf136, C6orf147, C8A, C8B, C9, C9orf57, CA12, CA14, CA4, CA9, CACFD1, CACHD1, CACNA1A, CACNA1B, CACNA1C, CACNA1D, CACNA1E, CACNA1F, CACNA1G, CACNA1H, CACNA1I, CACNA1S, CACNA2D1, CACNA2D2, CACNA2D3, CACNA2D4, CACNB3, CACNG3, CACNG5, CACNG6, CACNG7, CACNG8, CAD, CADM1, CADM2, CADM4, CALCOCO2, CALCR, CALHM4, CALHM5, CALHM6, CALM2, CALN1, CALR, CALU, CALY, CAMK2D, CAMK2G, CAMLG, CAND1, CANT1, CANX, CAPG, CAPN1, CAPNS1, CAPRIN1, CAPZA2, CAPZA3, CAPZB, CARMIL2, CASD1, CASK, CASR, CAST, CAT, CATSPER2, CATSPER4, CAV1, CBARP, CBFB, CC2D1A, CCDC107, CCDC115, CCDC126, CCDC127, CCDC134, CCDC136, CCDC163, CCDC167, CCDC168, CCDC188, CCDC197, CCDC47, CCDC77, CCDC80, CCDC88A, CCDC88B, CCDC90B, CCDC91, CCKAR, CCKBR, CCNB1, CCNB2, CCPG1, CCR10, CCR2, CCR3, CCR4, CCR5, CCR8, CD101, CD151, CD163, CD163L1, CD164, CD164L2, CD19, CD1A, CD1B, CD1E, CD200, CD200R1, CD200R1L, CD207, CD209, CD22, CD226, CD24, CD244, CD247, CD248, CD276, CD300A, CD300E, CD300LB, CD300LF, CD300LG, CD302, CD320, CD33, CD34, CD36, CD37, CD38, CD3D, CD3G, CD40, CD40LG, CD44, CD46, CD48, CD5, CD52, CD58, CD59, CD6, CD63, CD68, CD7, CD70, CD74, CD80, CD81, CD82, CD83, CD86, CD8B, CD8B2, CD9, CD93, CD96, CD99, CDAN1, CDC14B, CDC27, CDC42, CDC42BPA, CDC42BPB, CDC42EP2, CDC42EP5, CDC5L, CDCA7L, CDCP2, CDH1, CDH10, CDH11, CDH16, CDH17, CDH18, CDH19, CDH2, CDH20, CDH22, CDH23, CDH24, CDH26, CDH3, CDH5, CDH7, CDH8, CDH9, CDHR1, CDHR3, CDHR4, CDHR5, CDIPT, CDK1, CDK5, CDK5R1, CDK5R2, CDK5RAP2, CDK5RAP3, CDK9, CDKAL1, CDON, CDRT15L2, CDS1, CDS2, CDYL, CEACAM1, CEACAM19, CEACAM21, CEACAM4, CEACAM5, CEACAM6, CEACAM7, CELF1, CELSR1, CELSR2, CELSR3, CEMIP2, CEND1, CENPE, CEP170, CEP290, CEP350, CEP41, CEP55, CEP95, CEPT1, CERK, CERS1, CERS2, CERS3, CERS5, CERS6, CES5A, CFAP47, CFAP54, CFAP61, CFAP65, CFAP91, CFI, CFL1, CFTR, CGRRF1, CHD4, CHD5, CHERP, CHIC1, CHIC2, CHID1, CHL1, CHML, CHMP2A, CHMP6, CHN2, CHODL, CHP1, CHPF2, CHPT1, CHRFAM7A, CHRM1, CHRM2, CHRNA1, CHRNA10, CHRNA2, CHRNA3, CHRNA4, CHRNA5, CHRNA6, CHRNA7, CHRNB1, CHRNB2, CHRNB3, CHRNB4, CHRND, CHRNE, CHST1, CHST10, CHST11, CHST12, CHST13, CHST14, CHST15, CHST5, CHST7, CHST8, CHST9, CHSY1, CHSY3, CHTF18, CIB1, CIROP, CISD2, CIST1, CIT, CKAP4, CKAP5, CKLF, CKLF-CMTM1, CLASP1, CLASP2, CLCC1, CLCN1, CLCN2, CLCN3, CLCN4, CLCN5, CLCN6, CLCN7, CLCNKB, CLCP1, CLDN1, CLDN10, CLDN12, CLDN16, CLDN3, CLDN5, CLDND1, CLDND2, CLEC10A, CLEC12A, CLEC12B, CLEC14A, CLEC17A, CLEC1A, CLEC1B, CLEC2B, CLEC2D, CLEC2L, CLEC4A, CLEC4C, CLEC4D, CLEC4E, CLEC4F, CLEC4G, CLEC4M, CLEC5A, CLEC7A, CLEC9A, CLIC1, CLIC2, CLIC3, CLIC4, CLIC5, CLINT1, CLIP4, CLK3, CLMN, CLN3, CLN5, CLN6, CLN8, CLP1, CLPTM1, CLPTM1L, CLRN1, CLRN3, CLSTN1, CLSTN3, CLTA, CLTC, CLTCL1, CLYBL, CMAHP, CMAS, CMKLR1, CMTM1, CMTM2, CMTM3, CMTM4, CMTM5, CMTM6, CMTM7, CMTM8, CNGA3, CNGA4, CNGB1, CNGB3, CNIH1, CNIH2, CNIH4, CNKSR1, CNKSR2, CNKSR3, CNMD, CNN2, CNNM1, CNNM3, CNOT1, CNOT10, CNOT2, CNOT6, CNOT7, CNOT9, CNP, CNPPD1, CNST, CNTN1, CNTN6, CNTNAP1, CNTNAP2, CNTNAP3, CNTNAP3B, CNTNAP3C, CNTNAP4, CNTNAP5, CNTRL, COA1, COBL, COG1, COG2, COG3, COG4, COG5, COG8, COIL, COL15A1, COL17A1, COL1A1, COL25A1, COL4A1, COL4A2, COL4A3, COL4A4, COL4A5, COL4A6, COL6A1, COL6A2, COLCA1, COLEC12, COLGALT1, COMMD7, COMT, COMTD1, COP1, COPA, COPB1, COQ10B, COQ2, COQ7, COQ8A, CORO1A, CORO2B, CORO7, COX10, COX18, COX4I1, COX7B2, CPD, CPE, CPEB1, CPLANE1, CPM, CPN1, CPNE1, CPNE6, CPO, CPOX, CPSF2, CPSF6, CPSF7, CPT1A, CPT1B, CPT1C, CR1, CR1L, CR2, CRACR2A, CRB1, CRBN, CREB3, CREB3L1, CREB3L2, CREB3L3, CRELD1, CRHR1, CRHR2, CRIM1, CRISP3, CRK, CRLF2, CRLF3, CRLS1, CRNN, CS, CSE1L, CSF1, CSF1R, CSF2RA, CSF2RB, CSF3R, CSGALNACT2, CSMD1, CSMD2, CSMD3, CSNK1A1, CSNK1E, CSNK1G1, CSNK1G2, CSPG4, CSPG5, CSRNP1, CTAGE1, CTAGE15, CTAGE4, CTAGE6, CTAGE8, CTAGE9, CTDNEP1, CTH, CTNNB1, CTNNBL1, CTNS, CTPS1, CTSA, CTSC, CTSG, CTSW, CTXN1, CTXN2, CTXN3, CTXND1, CTXND2, CUBN, CUL3, CUL4B, CUTA, CUZD1, CWC27, CWH43, CX3CL1, CXCL13, CXCL16, CXCR2, CXCR3, CXCR4, CXCR5, CXorf66, CYB561, CYB561A3, CYB561D1, CYB5A, CYB5B, CYB5D2, CYB5R1, CYB5R2, CYB5R3, CYBA, CYBB, CYBC1, CYBRD1, CYC1, CYFIP2, CYP11A1, CYP11B2, CYP19A1, CYP1B1, CYP20A1, CYP21A2, CYP26C1, CYP2A6, CYP2A7, CYP2D6, CYP2D7, CYP2J2, CYP2S1, CYP2U1, CYP3A4, CYP3A43, CYP3A5, CYP4A11, CYP4A22, CYP4B1, CYP4F12, CYP4F2, CYP4F22, CYP4F8, CYP4Z2P, CYP51A1, CYP7B1, CYRIA, CYRIB, CYSLTR1, CYSTM1, CYTH2, CYYR1, DAAM1, DAB2IP, DAD1, DAG1, DAGLA, DAGLB, DAPK2, DAPL1, DAPP1, DARS1, DBH, DBNL, DCAF17, DCAKD, DCBLD1, DCBLD2, DCC, DCD, DCHS1, DCHS2, DCP1A, DCP1B, DCST1, DCST2, DCSTAMP, DCT, DCTN1, DCTN2, DCUN1D5, DCXR, DDHD2, DDOST, DDR1, DDRGK1, DDX1, DDX17, DDX18, DDX19A, DDX19B, DDX20, DDX21, DDX24, DDX39A, DDX3X, DDX3Y, DDX41, DDX42, DDX47, DDX5, DDX50, DDX51, DDX52, DDX54, DDX55, DDX56, DDX59, DDX6, DEF6, DEFB1, DEFB106A, DEFB106B, DEGS1, DENND5A, DENND5B, DEPDC5, DERL1, DERL2, DEUP1, DGAT1, DGAT2, DGCR2, DGKA, DGKE, DGKG, DGKI, DGKQ, DGKZ, DHCR24, DHCR7, DHODH, DHRS13, DHRS3, DHRS7, DHRS7B, DHX34, DHX36, DHX38, DHX9, DIABLO, DIO1, DIO2, DIP2A, DIP2B, DIRAS1, DIRAS2, DIS3, DISP1, DISP2, DISP3, DLC1, DLG1, DLG2, DLGAP4, DLK1, DLK2, DLL1, DLL3, DLL4, DLST, DMBT1, DMC1, DMD, DMRT2, DMTN, DNAH10, DNAJA1, DNAJA2, DNAJA4, DNAJB11, DNAJB12, DNAJB14, DNAJB6, DNAJC1, DNAJC10, DNAJC13, DNAJC14, DNAJC16, DNAJC18, DNAJC19, DNAJC22, DNAJC24, DNAJC25, DNAJC3, DNAJC4, DNAJC5, DNAJC5B, DNAJC5G, DNAJC7, DNM1L, DOC2B, DOCK1, DOCK10, DOCK2, DOCK4, DOCK7, DOCK8, DOCK9, DOLK, DOLPP1, DPAGT1, DPEP1, DPEP2, DPEP3, DPM1, DPM2, DPM3, DPP10, DPP4, DPP6, DPY19L1, DPY19L2, DPY19L2P1, DPY19L2P2, DPY19L3, DPY19L4, DPYSL2, DRAM1, DRAM2, DRC1, DRD3, DRD4, DRG1, DRG2, DSC1, DSC2, DSC3, DSCAM, DSCAML1, DSE, DSEL, DSG2, DSPP, DST, DTNA, DUOX1, DUOX2, DUOXA1, DUOXA2, DUSP13A, DYM, DYNAP, DYNC1H1, DYNC1LI1, DYNC1LI2, DYNLL1, DYNLL2, DYNLRB1, DYNLT2, DYRK2, DYSF, E2F5, EBPL, ECE1, ECE2, ECEL1, ECH1, ECHDC1, ECI2, ECPAS, ECRG4, EDA, EDA2R, EDAR, EDC3, EDC4, EDDM13, EDEM1, EDEM2, EDEM3, EED, EEF1A1, EEF1E1, EEF1G, EEF2, EFCAB14, EFNB2, EFTUD2, EGF, EGFL6, EGFR, EHBP1, EHBP1L1, EHD1, EHD2, EHD4, EHMT1, EI24, EIF2A, EIF2AK2, EIF2AK3, EIF2B1, EIF2S1, EIF3A, EIF3D, EIF3E, EIF3F, EIF3H, EIF3K, EIF3L, EIF4A1, EIF4A3, EIF4EBP3, EIF4ENIF1, EIF4G1, EIF4G2, EIF4H, EIF5A, ELAPOR2, ELAVL1, ELFN1, ELFN2, ELMO1, ELMO2, ELMOD2, ELOVL1, ELOVL2, ELOVL5, ELOVL7, ELP6, EMB, EMC1, EMC10, EMC3, EMC4, EMC6, EMC7, EMC8, EMCN, EMD, EML2, EML4, EMP1, EMP2, EMP3, ENDOD1, ENG, ENO1, ENO2, ENO3, ENPP1, ENPP2, ENPP4, ENPP5, ENPP6, ENPP7, ENTPD1, ENTPD3, ENTPD4, ENTPD5, ENTPD6, ENTPD7, ENTREP1, ENTREP2, ENTREP3, EOGT, EPB41, EPB41L3, EPGN, EPHA10, EPHA2, EPHA4, EPHA5, EPHA6, EPHA7, EPHB1, EPHB2, EPHB6, EPHX3, EPHX4, EPOR, EPPK1, EPRS1, EPS15, EPS15L1, ERAL1, ERAP1, ERAP2, ERBB2, ERBB3, ERBB4, ERC1, ERCC5, ERCC6L, ERG28, ERGIC1, ERGIC2, ERGIC3, ERMAP, ERMARD, ERMN, ERMP1, ERO1A, ERP29, ERVV-1, ERVV-2, ESAM, ESR1, ESYT1, ESYT2, ESYT3, ETFDH, ETNK1, ETV6, EVA1A, EVA1B, EVA1C, EVI2A, EVI2B, EVI5L, EVL, EVPL, EXD2, EXOC1, EXOC2, EXOC4, EXOC7, EXOC8, EXOG, EXOSC10, EXT1, EXT2, EYS, EZR, F11, F2RL1, F2RL3, F3, F5, F8, FA2H, FAAH, FAAH2, FABP6, FADS1, FADS2, FADS3, FADS6, FAF1, FAIM2, FAM118A, FAM120A, FAM151A, FAM156A, FAM156B, FAM162A, FAM162B, FAM163A, FAM163B, FAM171A2, FAM171B, FAM174A, FAM174C, FAM187A, FAM187B, FAM200A, FAM210A, FAM210B, FAM234A, FAM234B, FAM241A, FAM241B, FAM3A, FAM3D, FAM76B, FAM83B, FAM87A, FAM8A1, FAM9C, FANCI, FANCL, FAP, FARP1, FARSA, FARSB, FAS, FASLG, FASN, FAT1, FAT2, FAT3, FAT4, FAXC, FAXDC2, FBL, FBN2, FBP2, FBXL12, FBXL17, FBXL2, FBXW12, FBXW7, FCAR, FCER1A, FCER2, FCGR1A, FCGR2A, FCGR2B, FCGR2C, FCGR3A, FCGRT, FCHO2, FCMR, FCRL2, FDFT1, FDPS, FEN1, FER1L4, FER1L5, FER1L6, FERMT3, FES, FFAR2, FGFR1, FGFR2, FGFR3, FGFR4, FGFRL1, FHOD1, FIBCD1, FIBP, FIG4, FILIP1L, FIS1, FKBP10, FKBP11, FKBP15, FKBP1A, FKBP1B, FKBP2, FKBP5, FKBP8, FKBP9, FKRP, FKTN, FLG, FLNA, FLNB, FLNC, FLOT1, FLOT2, FLT1, FLT3, FLT3LG, FLT4, FLVCR1, FLVCR2, FMNL1, FMO2, FMR1, FMR1NB, FNBP1L, FNDC10, FNDC3A, FNDC3B, FNDC5, FNDC9, FOLH1, FOLR1, FOLR3, FPR1, FPR2, FPR3, FRAS1, FREM1, FREM3, FRMD3, FRMD5, FRMD8, FRRS1, FRS2, FRS3, FRZB, FSD1L, FSHR, FTH1, FTL, FUBP3, FURIN, FUT1, FUT3, FUT4, FUT6, FUT7, FUT8, FXR1, FXR2, FXYD2, FXYD3, FXYD5, FXYD6, FXYD6-FXYD2, FXYD6P3, FXYD7, FYCO1, FZD3, FZD6, FZD7, FZD8, FZD9, G3BP1, G6PC1, G6PC2, G6PC3, G6PD, GAA, GAB3, GABARAP, GABARAPL1, GABARAPL2, GABBR1, GABBR2, GABRA1, GABRA2, GABRA4, GABRA5, GABRA6, GABRB1, GABRB2, GABRB3, GABRD, GABRG2, GABRG3, GABRP, GAK, GAL3ST1, GAL3ST2, GAL3ST3, GAL3ST4, GALK1, GALNT1, GALNT11, GALNT13, GALNT14, GALNT15, GALNT2, GALNT3, GALNT7, GALNT9, GALNTL5, GALNTL6, GALR1, GALR2, GALR3, GANAB, GAPDH, GAPVD1, GARIN2, GAS1, GAS2, GASK1A, GASK1B, GBA2, GBF1, GBGT1, GBP3, GBP5, GC, GCC2, GCGR, GCN1, GCNT1, GCNT2, GCNT3, GDAP1, GDAP1L1, GDE1, GDI2, GDPD1, GDPD3, GDPD4, GDPD5, GEMIN4, GEMIN5, GET1, GGA1, GGA3, GGCX, GGNBP1, GGT1, GGT3P, GGT5, GGT6, GGT7, GGTA1, GHDC, GHITM, GHR, GHRHR, GHSR, GIGYF2, GIMAP1-GIMAP5, GIMAP2, GINM1, GIPC1, GIPR, GIT1, GLA, GLE1, GLG1, GLI2, GLIPR1, GLIPR1L2, GLMP, GLP1R, GLP2R, GLRA1, GLRA2, GLRA3, GLT6D1, GLT8D1, GLT8D2, GNA13, GNAI1, GNAI2, GNAI3, GNAL, GNAO1, GNAQ, GNAS, GNAT1, GNB1, GNB2, GNB5, GNG2, GNG5, GNL2, GNL3, GNL3L, GNPAT, GNPTAB, GNRHR, GNRHR2, GOLGA3, GOLGA5, GOLGB1, GOLIM4, GOLM1, GOLM2, GOLPH3, GOLT1A, GOLT1B, GOPC, GORASP2, GOSR1, GOSR2, GP1BA, GP1BB, GP9, GPAA1, GPAT2, GPAT4, GPC5, GPD2, GPER1, GPI, GPM6A, GPM6B, GPNMB, GPR107, GPR108, GPR132, GPR137, GPR137B, GPR137C, GPR139, GPR141, GPR143, GPR148, GPR149, GPR15, GPR153, GPR155, GPR156, GPR160, GPR161, GPR162, GPR17, GPR171, GPR173, GPR18, GPR180, GPR182, GPR19, GPR34, GPR37L1, GPR39, GPR45, GPR52, GPR55, GPR61, GPR62, GPR63, GPR65, GPR68, GPR78, GPR89A, GPR89B, GPRC5B, GPRC5C, GPSM1, GPSM2, GPX8, GRAMD1A, GRAMD1B, GRAMD1C, GRAMD2B, GRAMD4, GRAP, GREB1, GREB1L, GRHL2, GRIA1, GRIA2, GRIA4, GRID2, GRIK2, GRIK3, GRIK4, GRIK5, GRIN1, GRIN2A, GRIN2B, GRIN2C, GRIN3A, GRINA, GRIP2, GRK1, GRK2, GRK6, GRK7, GRM2, GRM3, GRM4, GRM5, GRM7, GRM8, GRN, GSDMA, GSDMD, GSDME, GSG1, GSG1L, GSG1L2, GSTK1, GTF2I, GTF3C1, GTF3C3, GTPBP1, GTPBP4, GTSCR1, GTSE1, GUSB, GXYLT1, GXYLT2, GYG1, GYPA, GYPB, GYPC, GYPE, GYS1, GZMB, GZMH, GZMM, H3C1, H3C10, H3C11, H3C12, H3C2, H3C3, H3C4, H3C6, H3C7, H3C8, H4C1, H4C11, H4C12, H4C13, H4C14, H4C15, H4C16, H4C2, H4C3, H4C4, H4C5, H4C6, H4C8, H4C9, HACD1, HACD2, HACD3, HACE1, HAS1, HAS3, HAVCR2, HBA2, HBB, HBD, HBS1L, HCAR1, HCAR2, HCAR3, HCCS, HCFC1, HCLS1, HCN1, HCRTR1, HCST, HDAC2, HDC, HEATR1, HEATR5B, HECA, HECTD4, HEG1, HELZ, HELZ2, HEPACAM, HEPACAM2, HEPH, HEPHL1, HERC1, HERC2, HERPUD1, HERPUD2, HEXA, HEXB, HFE, HGF, HGSNAT, HHAT, HHATL, HHIPL1, HHLA2, HID1, HIGD1A, HIGD1B, HIGD1C, HIGD2B, HILPDA, HIP1, HK2, HLA-A, HLA-B, HLA-C, HLA-DMA, HLA-DMB, HLA-DOB, HLA-DPA1, HLA-DPB1, HLA-DQA1, HLA-DQA2, HLA-DQB1, HLA-DRA, HLA-DRB1, HLA-DRB3, HLA-DRB5, HLA-E, HLA-F, HLA-G, HLA-H, HLTF, HM13, HMCN2, HMGCLL1, HMGCR, HMMR, HMOX1, HMOX2, HMX3, HNRNPA1, HNRNPA2B1, HNRNPC, HNRNPF, HNRNPH1, HNRNPH2, HNRNPK, HNRNPL, HNRNPLL, HNRNPM, HNRNPU, HNRNPUL2, HOGA1, HPCA, HPCAL1, HPN, HPS4, HPS6, HPSE, HPSE2, HRAS, HRCT1, HRK, HS2ST1, HS3ST2, HS3ST3A1, HS3ST5, HS6ST1, HS6ST2, HS6ST3, HSD11B1, HSD11B2, HSD17B12, HSD17B2, HSD17B4, HSD3B2, HSDL2, HSP90AA1, HSP90AB1, HSP90B1, HSPA14, HSPA2, HSPA5, HSPA8, HSPD1, HSPE1, HSPG2, HTATIP2, HTR3A, HTR3B, HTR3E, HTR4, HTRA2, HUWE1, HVCN1, HYAL4, HYOU1, IARS1, IARS2, IBSP, IBTK, ICA1, ICAM1, ICAM2, ICAM3, ICAM4, ICAM5, ICMT, ICOS, ICOSLG, IDO2, IER3, IER3IP1, IFI16, IFI27, IFI27L1, IFI27L2, IFI35, IFI6, IFITM1, IFITM10, IFITM2, IFITM3, IFNAR2, IFNAR2-IL10RB, IFNGR1, IFNGR2, IFNK, IFNLR1, IFT122, IGDCC3, IGF1R, IGF2R, IGHMBP2, IGLL1, IGSF1, IGSF11, IGSF23, IGSF3, IGSF6, IGSF8, IGSF9B, IKBIP, IL10RA, IL10RB, IL11RA, IL12B, IL12RB2, IL13RA1, IL13RA2, IL15RA, IL17RA, IL17RB, IL17RC, IL17RE, IL18BP, IL18R1, IL1R1, IL1R2, IL1RAP, IL1RAPL1, IL20RA, IL20RB, IL21R, IL23R, IL2RA, IL2RB, IL2RG, IL31RA, IL32, IL33, IL3RA, IL4R, IL5RA, IL6R, IL6ST, IL9R, ILDR2, ILF2, ILF3, ILK, ILVBL, IMMP2L, IMMT, IMP3, IMP4, IMPDH2, IMPG2, INAFM1, INAFM2, INPP4A, INPP4B, INPP5A, INPP5B, INPP5D, INPP5F, INPP5K, INPPL1, INSR, INSRR, INTS1, INTS14, INTS2, INTS5, INVS, IPO4, IPO5, IPO7, IPO9, IQGAP2, IQSEC1, IRAG1, IRAG2, IRAK1, IRF4, IRGC, IRGM, ITCH, ITFG1, ITGA1, ITGA11, ITGA2, ITGA2B, ITGA3, ITGA4, ITGA5, ITGA6, ITGA7, ITGA8, ITGA9, ITGAE, ITGAL, ITGAM, ITGAV, ITGAX, ITGB1, ITGB1BP1, ITGB2, ITGB3, ITGB3BP, ITGB4, ITGB5, ITGB6, ITGB7, ITM2A, ITM2B, ITM2C, ITPKB, ITPR1, ITPR2, ITPR3, ITPRIP, ITPRIPL1, ITPRIPL2, ITSN1, IZUMO1, IZUMO2, IZUMO3, JAG1, JAK1, JAK2, JAK3, JAKMIP1, JAKMIP3, JAM2, JAML, JKAMP, JOSD1, JPH3, JTB, JUP, KANTR, KATNB1, KBTBD11-OT1, KBTBD6, KCNA1, KCNA10, KCNA2, KCNA3, KCNA4, KCNA5, KCNA6, KCNA7, KCNAB1, KCNAB2, KCNB1, KCNB2, KCNC1, KCNC2, KCNC3, KCNC4, KCND3, KCNE3, KCNE4, KCNE5, KCNF1, KCNG1, KCNG2, KCNG3, KCNG4, KCNH1, KCNH2, KCNH3, KCNH4, KCNH5, KCNH8, KCNJ10, KCNJ11, KCNJ12, KCNJ13, KCNJ15, KCNJ16, KCNJ17, KCNJ2, KCNJ3, KCNJ4, KCNJ5, KCNJ8, KCNK1, KCNK10, KCNK16, KCNK17, KCNK2, KCNK3, KCNK4, KCNK5, KCNK6, KCNK7, KCNMA1, KCNMB2, KCNMB3, KCNMB4, KCNN1, KCNN2, KCNN3, KCNN4, KCNQ1, KCNQ2, KCNQ3, KCNQ5, KCNS1, KCNS2, KCNS3, KCNT1, KCNT2, KCNU1, KCNV1, KCNV2, KCTD20, KCTD8, KDELR2, KDM3A, KDSR, KEL, KHDC1, KHDRBS1, KHSRP, KIAA0040, KIAA0319, KIAA0319L, KIAA1549, KIAA1549L, KIAA2013, KIDINS220, KIF11, KIF14, KIF15, KIF2A, KIF2C, KIF3B, KIF4A, KIF5A, KIF5B, KIFC1, KIR2DL1, KIR2DL2, KIR2DL3, KIR2DL4, KIR2DL5A, KIR2DL5B, KIR2DP1, KIR2DS1, KIR2DS2, KIR2DS3, KIR2DS4, KIR2DS5, KIR3DL1, KIR3DL2, KIR3DL3, KIR3DS1, KIRREL1, KIRREL2, KIRREL3, KISS1R, KIT, KITLG, KIZ, KL, KLB, KLC1, KLC2, KLHDC7A, KLHL2, KLHL23, KLRB1, KLRC1, KLRC2, KLRC4-KLRK1, KLRD1, KLRF1, KLRG1, KLRG2, KLRK1, KMO, KMT2E, KNCN, KPNA2, KPNA4, KPNA6, KPNB1, KRAS, KREMEN1, KREMEN2, KRR1, KRT1, KRT10, KRT10-AS1, KRT2, KRT5, KRT6A, KRT9, KRTCAP2, KRTCAP3, KSR1, KSR2, KTN1, L1CAM, L2HGDH, LACTBL1, LAIR1, LAMA1, LAMA2, LAMA3, LAMA4, LAMC3, LAMP1, LAMP2, LAPTM4A, LAPTM4B, LAPTM5, LARGE1, LARGE2, LARP1, LARP4, LARP4B, LAS1L, LASP1NB, LAT, LAX1, LAYN, LBH, LBP, LBR, LCAT, LCLAT1, LCTL, LDHA, LDHB, LDHC, LDLR, LDLRAD1, LDLRAD2, LDLRAD3, LDLRAD4, LEMD1, LEMD2, LEMD3, LEPR, LEPROTL1, LGALS16, LGALS3, LGALS3BP, LGALS8, LGSN, LHFPL1, LHFPL2, LHFPL3, LHFPL4, LHFPL5, LHFPL6, LHFPL7, LILRA6, LILRB1, LILRB2, LILRB3, LILRB4, LILRB5, LIM2, LIME1, LIMK1, LIMK2, LINC00052, LINC00301, LINC00477, LINC00596, LINC00862, LINC02912, LINGO2, LINGO3, LINGO4, LIPE, LITAFD, LMAN1, LMAN1L, LMAN2, LMAN2L, LMBR1, LMBR1L, LMBRD1, LMBRD2, LMF1, LMF2, LMLN, LMNB1, LMO7, LMOD1, LMTK2, LMTK3, LNPEP, LNPK, LOC101929829, LOC102723532, LOC102725023, LOC112268354, LOC112268355, LOC112694756, LOC124900568, LOC124900573, LOC124900574, LOC124905359, LOC128031833, LOC128092249, LOC128125816, LOC128125818, LOC128706665, LOC128706666, LOC728138, LOC728392, LONP1, LONP2, LOXL2, LOXL3, LOXL4, LPAR2, LPAR5, LPCAT1, LPCAT2, LPCAT3, LPCAT4, LPGAT1, LPXN, LRBA, LRFN1, LRFN2, LRFN4, LRFN5, LRG1, LRIG1, LRIT2, LRIT3, LRP1, LRP10, LRP11, LRP12, LRP1B, LRP2, LRP3, LRP4, LRP5, LRP6, LRP8, LRPPRC, LRRC1, LRRC19, LRRC24, LRRC25, LRRC3, LRRC37A, LRRC37A2, LRRC37A3, LRRC37B, LRRC3B, LRRC3C, LRRC4, LRRC40, LRRC41, LRRC4C, LRRC53, LRRC57, LRRC59, LRRC63, LRRC66, LRRC70, LRRC8A, LRRC8B, LRRC8C, LRRC8D, LRRC8E, LRRIQ4, LRRK1, LRRN1, LRRN2, LRRN3, LRRN4, LRRN4CL, LRRTM4, LRSAM1, LRTM1, LRTM2, LSG1, LSM4, LSMEM1, LSMEM2, LSP1, LSR, LSS, LST1, LTA, LTB, LTB4R2, LTC4S, LTK, LUZP1, LVRN, LY6D, LY6G5C, LY6G6C, LY75, LY9, LYN, LYPD3, LYPD5, LYPLA1, LYSMD4, LYST, LYVE1, LZTFL1, M1AP, M6PR, MACF1, MADCAM1, MADD, MAFA, MAG, MAGEA8, MAGED2, MAGI1, MAGI2, MAGI3, MAGT1, MAL, MAL2, MALL, MALRD1, MALT1, MAMDC2, MAMDC4, MAN1A1, MAN1A2, MAN1B1, MAN1C1, MAN2A1, MAN2A2, MANBAL, MANEAL, MANSC1, MANSC4, MAOA, MAP1LC3B, MAP2K1, MAP2K2, MAP2K3, MAP3K11, MAP3K12, MAP3K13, MAP4K1, MAP4K2, MAP7D3, MAPK10, MARCHF11, MARCHF5, MARCHF6, MARCKS, MARCO, MARF1, MARK2, MARS1, MARVELD1, MARVELD2, MARVELD3, MAS1L, MAST1, MATK, MATR3, MBOAT1, MBOAT2, MBOAT4, MBOAT7, MBTPS1, MBTPS2, MC1R, MC4R, MCAM, MCEMP1, MCF2, MCL1, MCM2, MCM3, MCM3AP, MCM4, MCM5, MCM7, MCOLN1, MCOLN2, MCOLN3, MCTP1, MCTP2, MCU, MCUB, MCUR1, MDGA1, MDGA2, MDH2, MDN1, ME1, ME2, ME3, MEAK7, MED1, MED12, MED13, MED14, MED15, MED16, MED17, MED28, MED4, MED6, MEGF11, MEGF8, MEGF9, MELK, MEMO1, MEP1A, MEP1B, MERTK, MEST, MET, METTL15, METTL25B, METTL2B, MFAP3L, MFF, MFGE8, MFN1, MFNG, MFRP, MFSD1, MFSD10, MFSD11, MFSD12, MFSD13A, MFSD14A, MFSD14B, MFSD14CP, MFSD2A, MFSD2B, MFSD3, MFSD4A, MFSD4B, MFSD5, MFSD6, MFSD6L, MFSD8, MFSD9, MGAM, MGAM2, MGAT1, MGAT2, MGAT3, MGAT4D, MGAT5, MGAT5B, MGLL, MGMT, MGRN1, MGST1, MGST2, MGST3, MIA2, MIA3, MICA, MICU3, MID1, MIEF1, MIGA1, MINAR1, MIP, MIR17HG, MISFA, MITD1, MKI67, MKKS, MKS1, MLC1, MLEC, MLF2, MLH1, MMAA, MMD, MME, MMEL1, MMGT1, MMP13, MMP14, MMP15, MMP20, MMP21, MMP23B, MMP24, MMP25, MMS19, MOB4, MOG, MOGS, MOSMO, MOSPD2, MOSPD3, MPDU1, MPDZ, MPG, MPHOSPH9, MPIG6B, MPL, MPP1, MPP2, MPP7, MPPE1, MPV17, MPV17L2, MPZL1, MPZL2, MPZL3, MR1, MRAS, MRC2, MRGPRX2, MROH7, MRPL42, MRS2, MS4A1, MS4A10, MS4A12, MS4A13, MS4A14, MS4A15, MS4A18, MS4A2, MS4A4A, MS4A4E, MS4A5, MS4A6A, MS4A6E, MS4A7, MS4A8, MSANTD3-TMEFF1, MSH2, MSH3, MSLN, MSLNL, MSMO1, MSR1, MSRA, MST1R, MT-CO2, MT-CYB, MTA2, MTARC1, MTARC2, MTCH1, MTCH2, MTCL1, MTCL2, MTCL3, MTDH, MTFP1, MTHFD1, MTHFD1L, MTM1, MTMR1, MTMR2, MTMR3, MTMR4, MTMR7, MTNAP1, MTNR1B, MTOR, MTX1, MUC1, MUC12, MUC15, MUC16, MUC17, MUC21, MUC22, MUC3A, MUC3B, MUC4, MUCL1, MUCL3, MUL1, MVP, MX1, MX2, MXRA7, MYADM, MYADML2, MYB, MYBBP1A, MYC, MYCBP2, MYCBPAP, MYCN, MYCT1, MYH14, MYH7B, MYH9, MYL6, MYLK4, MYO15A, MYO18A, MYO19, MYO1C, MYO1G, MYO5A, MYO5B, MYO5C, MYO6, MYO7A, MYO7B, MYO9A, MYO9B, MYORG, MYPN, MYRF, MYRFL, MYT1, N4BP2L2, NAA10, NAA15, NAAA, NAALAD2, NAALADL1, NAALADL2, NAGPA, NALCN, NALF2, NAP1L1, NAPA, NAPB, NAPG, NAT1, NAT10, NAT14, NAT2, NAT8, NAT8B, NBAS, NBEA, NBEAL1, NBEAL2, NBPF10, NBR1, NCAM1, NCAM2, NCAPD2, NCAPD3, NCAPG, NCAPG2, NCAPH, NCAPH2, NCDN, NCEH1, NCF1, NCF2, NCF4, NCKAP1L, NCL, NCLN, NCOR1, NCOR2, NCS1, NCSTN, NDC1, NDC80, NDE1, NDFIP2, NDRG2, NDRG4, NDST1, NDST2, NDUFA12, NDUFA4L2, NDUFAF2, NDUFAF4, NDUFAF6, NDUFS1, NDUFS8, NECTIN1, NECTIN2, NECTIN3, NELFCD, NELL2, NENF, NEO1, NET1, NETO2, NEU1, NEU2, NEU3, NEU4, NF1, NF2, NFAM1, NFASC, NFAT5, NFXL1, NGEF, NGFR, NHERF1, NIBAN1, NIBAN2, NID2, NINJ1, NINJ2, NIPA1, NIPA2, NIPAL1, NIPAL2, NIPAL3, NIPAL4, NISCH, NKG7, NKPD1, NLGN1, NLGN2, NLGN3, NLGN4X, NLGN4Y, NLRP3, NMB, NMD3, NME1, NMI, NMT1, NMT2, NMUR1, NMUR2, NNAT, NNT, NOL3, NOL9, NOMO1, NONO, NOP14, NOP56, NOP58, NOTCH1, NOTCH2, NOX1, NOX4, NOX5, NPBWR1, NPBWR2, NPC1, NPC1L1, NPDC1, NPEPPS, NPHP1, NPHS2, NPIPA1, NPIPB11, NPIPB12, NPIPB13, NPIPB3, NPIPB4, NPIPB5, NPM1, NPNT, NPR1, NPR2, NPR3, NPSR1, NPTN, NPTXR, NPY1R, NPY4R, NPY6R, NQO1, NR0B1, NR3C1, NRAS, NRBP1, NRCAM, NRG1, NRG2, NRG3, NRG4, NRK, NRM, NRN1, NRN1L, NRP1, NRP2, NRSN1, NRSN2, NRXN1, NRXN2, NRXN3, NSG1, NSG2, NSMF, NT5DC1, NT5E, NTPCR, NTRK1, NTRK2, NTRK3, NTT, NUCB1, NUCB2, NUDC, NUF2, NUFIP2, NUP107, NUP133, NUP153, NUP155, NUP188, NUP205, NUP210, NUP210L, NUP85, NUP93, NUP98, NVL, NXPE1, NXPE2, NYNRIN, OAS1, OAS2, OAS3, OASL, OCA2, OCEL1, OCIAD1, OCLN, OCRL, OCSTAMP, ODCP, ODF4, ODR4, OFD1, OGA, OGFOD3, OGFR, OGFRL1, OGT, OLA1, OLFM2, OLR1, OMA1, OPA1, OPN1LW, OPN1MW, OPN1MW2, OPN1SW, OPN3, OPN4, OPN5, OPRD1, OPRK1, OPRM1, OR10A5, OR10D3, OR10G3, OR10G4, OR10G6, OR10G7, OR10G8, OR10G9, OR10H1, OR10H2, OR10H3, OR10H4, OR10H5, OR10J1, OR10J3, OR10J4, OR10J5, OR10K1, OR10K2, OR10R2, OR10S1, OR10T2, OR10V1, OR10Z1, OR11H1, OR11H12, OR11H2, OR12D1, OR12D2, OR12D3, OR13D1, OR13G1, OR13H1, OR14A2, OR14C36, OR1A1, OR1A2, OR1B1, OR1C1, OR1D2, OR1D4, OR1D5, OR1E2, OR1F1, OR1G1, OR1I1, OR1J1, OR1J2, OR1J4, OR1K1, OR1L1, OR1L3, OR1L4, OR1L6, OR1L8, OR1M1, OR1N1, OR1N2, OR1Q1, OR1R1P, OR1S1, OR1S2, OR2A25, OR2A4, OR2A7, OR2AG1, OR2AG2, OR2B11, OR2D2, OR2F1, OR2G2, OR2I1P, OR2M4, OR2M5, OR2S2, OR3A1, OR3A2, OR3A3, OR3A4P, OR3A5P, OR4A15, OR4A16, OR4A47, OR4A5, OR4B1, OR4C11, OR4C12, OR4C15, OR4C16, OR4C3, OR4C46, OR4C5, OR4C6, OR4D1, OR4D10, OR4D11, OR4D2, OR4D5, OR4D6, OR4D9, OR4E1, OR4E2, OR4F15, OR4F16, OR4F17, OR4F21, OR4F3, OR4F4, OR4F5, OR4F6, OR4K1, OR4K13, OR4K14, OR4K15, OR4K17, OR4K2, OR4K3, OR4K5, OR4L1, OR4M1, OR4M2, OR4M2B, OR4N2, OR4N4, OR4N4C, OR4N5, OR4P4, OR4Q2, OR4Q3, OR4S1, OR4S2, OR4X1, OR4X2, OR51A2, OR51A4, OR51B2, OR51B4, OR51B5, OR51B6, OR51C1P, OR51D1, OR51E1, OR51E2, OR51F1, OR51F2, OR51G1, OR51G2, OR51H1, OR51I1, OR51I2, OR51J1, OR51L1, OR51M1, OR51Q1, OR51S1, OR51T1, OR51V1, OR52A1, OR52A5, OR52B2, OR52B4, OR52B6, OR52D1, OR52E1, OR52E2, OR52E4, OR52E5, OR52E6, OR52E8, OR52H1, OR52I1, OR52I2, OR52J3, OR52K1, OR52K2, OR52L1, OR52M1, OR52N1, OR52N2, OR52N4, OR52N5, OR52P1, OR52R1, OR52W1, OR56A1, OR56A3, OR56A4, OR56A5, OR56B1, OR56B2P, OR56B4, OR5AC2, OR5AK2, OR5AL1, OR5AN1, OR5AP2, OR5B12, OR5B17, OR5B2, OR5B21, OR5B3, OR5D13, OR5D14, OR5D16, OR5D18, OR5D3P, OR5F1, OR5I1, OR5L1, OR5M1, OR5M10, OR5M11, OR5M8, OR5M9, OR5T1, OR5T2, OR5T3, OR5W2, OR6A2, OR6B2, OR6C2, OR6C3, OR6K2, OR6K3, OR6K6, OR6N2, OR7A10, OR7A17, OR7A5, OR7C1, OR7C2, OR7D2, OR7D4, OR7E24, OR7G1, OR7G2, OR7G3, OR8A1, OR8B12, OR8B2, OR8B3, OR8B4, OR8B8, OR8D1, OR8D2, OR8D4, OR8G1, OR8G3P, OR8G5, OR8H1, OR8H2, OR8H3, OR8I2, OR8J1, OR8J2, OR8J3, OR8K1, OR8K3, OR8K5, OR8S1, OR8U1, OR8U8, OR8U9, OR9G1, OR9G4, OR9G9, OR9I1, OR9Q1, OR9Q2, ORAI1, ORAI2, ORAI3, ORC1, ORC2, ORC6, ORMDL2, OSBP, OSBP2, OSBPL10, OSBPL11, OSBPL3, OSBPL5, OSBPL8, OSBPL9, OSMR, OSTC, OSTM1, OTOA, OTOF, OTOP1, OTOP2, OTOP3, OTUD4, OXA1L, OXER1, OXGR1, OXTR, P2RX1, P2RX2, P2RX3, P2RX4, P2RX5, P2RX6, P2RX7, P2RY12, P2RY14, P2RY8, P3H1, P4HA1, P4HTM, PA2G4, PAAF1, PABPC1, PACRG, PAF1, PAFAH1B3, PAFAH2, PAICS, PAK2, PALM3, PALMD, PALS2, PAM, PAN2, PANK2, PANX1, PANX2, PAPOLA, PAPOLG, PAQR3, PAQR4, PAQR5, PAQR6, PAQR8, PAQR9, PARK7, PARL, PARM1, PARP1, PARP14, PARP16, PARP4, PARP9, PATJ, PAX6, PBXIP1, PCBP1, PCBP2, PCDH1, PCDH10, PCDH11Y, PCDH12, PCDH15, PCDH17, PCDH18, PCDH19, PCDHA3, PCDHA4, PCDHA8, PCDHAC1, PCDHB10, PCDHB11, PCDHB13, PCDHB14, PCDHB15, PCDHB16, PCDHB2, PCDHB3, PCDHB4, PCDHB5, PCDHB6, PCDHB7, PCDHB9, PCDHGA10, PCDHGA3, PCDHGA6, PCDHGB1, PCDHGB4, PCDHGC3, PCDHGC4, PCDHGC5, PCGF3, PCLO, PCM1, PCMTD1, PCNT, PCNX1, PCNX2, PCNX3, PCNX4, PCSK1, PCSK2, PCSK4, PCSK5, PCSK6, PCSK7, PCYOX1L, PCYT1A, PDCD1, PDCD2L, PDCD6IP, PDE3A, PDE3B, PDE4A, PDE4D, PDE6B, PDGFA, PDGFB, PDGFRA, PDGFRB, PDLIM5, PDP1, PDPK2P, PDPN, PDZD8, PDZK1, PDZK1IP1, PEAR1, PEBP4, PEDS1, PEDS1-UBE2V1, PEF1, PEG10, PELP1, PEMT, PES1, PET100, PEX11B, PEX13, PEX14, PEX16, PEX19, PEX2, PEX3, PEX5, PEX5L, PFDN4, PFKL, PFKM, PFKP, PFN1, PFN2, PGAM1, PGAP1, PGAP2, PGBD1, PGF, PGK1, PGLYRP2, PGLYRP3, PGLYRP4, PGRMC1, PGRMC2, PHB1, PHB2, PHEX, PHLDA2, PHLDA3, PHLDB2, PHRF1, PHTF1, PHTF2, PI4K2A, PI4K2B, PI4KA, PI4KB, PIANP, PICALM, PICK1, PIEZO1, PIEZO2, PIGA, PIGB, PIGF, PIGG, PIGK, PIGN, PIGO, PIGP, PIGQ, PIGS, PIGT, PIGU, PIGV, PIGW, PIK3AP1, PIK3C2A, PIK3C2G, PIK3C3, PIK3CG, PIK3R1, PIK3R4, PIK3R5, PIK3R6, PILRA, PILRB, PINK1, PIRT, PITPNM1, PITPNM2, PITPNM3, PJVK, PKD1, PKD1L1, PKD1L2, PKD1L3, PKD2, PKD2L1, PKD2L2, PKDREJ, PKHD1L1, PKMYT1, PKN2, PKP2, PLA2G15, PLA2G4C, PLA2G4D, PLA2G4E, PLA2G4F, PLA2G6, PLAAT1, PLAAT2, PLAAT4, PLAUR, PLB1, PLCB3, PLCD4, PLCH1, PLD1, PLD3, PLD4, PLD5, PLEK, PLEKHA1, PLEKHA2, PLEKHA4, PLEKHA5, PLEKHB1, PLEKHB2, PLEKHO1, PLIN1, PLIN2, PLIN3, PLLP, PLN, PLP1, PLP2, PLPP1, PLPP2, PLPP3, PLPP4, PLPP5, PLPP6, PLPP7, PLPPR1, PLPPR2, PLPPR3, PLPPR4, PLPPR5, PLRG1, PLSCR1, PLSCR2, PLSCR4, PLVAP, PLXDC1, PLXDC2, PLXNA4, PLXNC1, PLXND1, PMEL, PMEPA1, PMIS2, PMP22, PMVK, PNKD, PNKP, PNN, PNPLA1, PNPLA2, PNPLA3, PNPLA4, PNPLA5, PNPLA6, PNPLA8, PODXL, PODXL2, POFUT1, POLD1, POLR2B, POLR3A, POMGNT1, POMK, POMP, POMT1, POMT2, PON2, POP1, POPDC2, POPDC3, POR, PORCN, POTEE, POTEF, POTEH, POTEI, POTEJ, POTEKP, POTEM, PPAN-P2RY11, PPIA, PPIB, PPIF, PPIL3, PPL, PPM1A, PPM1B, PPM1G, PPM1L, PPP1R14C, PPP1R14D, PPP1R15A, PPP1R21, PPP1R3A, PPP1R3F, PPP2CA, PPP2R1A, PPP2R2B, PPP2R5C, PPT1, PPT2, PPT2-EGFL8, PRAC2, PRAF2, PRCD, PRDX6, PREB, PREP, PRF1, PRG1, PRG2, PRG4, PRICKLE1, PRIM1, PRKAA2, PRKACA, PRKACB, PRKAG1, PRKAG2, PRKAR1A, PRKAR2A, PRKCA, PRKCB, PRKCD, PRKCH, PRKCI, PRKCZ, PRKD1, PRKD2, PRKD3, PRKDC, PRKRA, PRLHR, PRLR, PRMT3, PRNP, PRPF19, PRPF40A, PRPF6, PRPF8, PRPH, PRPH2, PRPS1, PRR11, PRR7, PRRC2A, PRRC2C, PRRG1, PRRG2, PRRG3, PRRG4, PRRT1, PRRT1B, PRRT2, PRRT3, PRRT4, PRSS16, PRSS21, PRSS22, PRTG, PRUNE2, PSAP, PSD4, PSEN1, PSEN2, PSENEN, PSMB2, PSMC1, PSMC2, PSMC3, PSMC4, PSMC5, PSMC6, PSMD1, PSMD11, PSMD12, PSMD13, PSMD2, PSMD3, PSMD7, PSME2, PSME3, PSMF1, PSTPIP1, PSTPIP2, PTAFR, PTBP1, PTBP2, PTCH1, PTCH2, PTCHD1, PTCHD3, PTCHD4, PTCRA, PTDSS1, PTDSS2, PTGDR, PTGER2, PTGER3, PTGER4, PTGES, PTGES2, PTGFRN, PTGIR, PTH2, PTH2R, PTK6, PTK7, PTPA, PTPN1, PTPN2, PTPN5, PTPN6, PTPRA, PTPRB, PTPRC, PTPRCAP, PTPRD, PTPRE, PTPRF, PTPRG, PTPRK, PTPRM, PTPRN, PTPRN2, PTPRO, PTPRQ, PTPRS, PTPRT, PTPRZ1, PTRH2, PTTG1IP, PTTG1IP2, PVR, PVRIG, PXMP2, PYGB, QARS1, QPCTL, QRFPR, QSOX2, RAB10, RAB11FIP1, RAB11FIP5, RAB12, RAB15, RAB1A, RAB1B, RAB1C, RAB24, RAB27A, RAB30, RAB32, RAB38, RAB3A, RAB40AL, RAB40B, RAB40C, RAB42, RAB4A, RAB5A, RAB5B, RAB6A, RABAC1, RABGAP1L, RABIF, RAC1, RAD21, RAD50, RAET1E, RAG2, RALA, RALB, RALBP1, RAMP1, RAMP2, RAMP3, RAN, RANBP2, RANBP9, RAP1B, RAP1GAP, RAP2A, RAP2B, RAP2C, RAPGEF2, RAPGEF3, RAPGEF4, RAPGEFL1, RARG, RARRES1, RARS1, RASAL3, RASGRP1, RASGRP4, RAX, RBM15B, RBM19, RBM23, RBMX, RBMXP1, RC3H2, RCAN2, RCE1, RCVRN, RDH10, RDH14, RDH8, RDX, RECK, RECQL, RECQL4, REELD1, REEP1, REEP2, REEP3, REEP4, REEP5, REEP6, REG3A, RELCH, RELL1, REN, RER1, RET, RETREG1, RETREG2, RETSAT, RFFL, RFNG, RGP1, RGR, RGS14, RGS16, RGS17, RGS19, RGS5, RGS6, RGS7, RGS8, RGS9, RGS9BP, RGSL1, RHAG, RHBDD1, RHBDD3, RHBDL1, RHBDL3, RHBG, RHCE, RHD, RHEB, RHEBL1, RHEX, RHO, RHOC, RHOT1, RHOT2, RIC1, RIC3, RILPL2, RIMS1, RIMS2, RIMS3, RIMS4, RIN1, RIPK4, RIPOR1, RIT1, RIT2, RMDN2, RMDN3, RNASEK, RNASEK-C17orf49, RND3, RNF112, RNF121, RNF122, RNF128, RNF13, RNF130, RNF139, RNF141, RNF144A, RNF148, RNF149, RNF150, RNF167, RNF170, RNF175, RNF182, RNF185, RNF19A, RNF213, RNF215, RNF217, RNF222, RNF223, RNF225, RNF228, RNF24, RNF32-DT, RNF34, RNF40, RNF8, RNFT1, RNFT2, RNPS1, ROBO2, ROBO3, ROBO4, ROCK1, ROR1, ROR2, ROS1, RPE65, RPH3A, RPIA, RPL10, RPL10A, RPL10L, RPL11, RPL12, RPL13, RPL13A, RPL14, RPL18, RPL18A, RPL19, RPL21, RPL23, RPL24, RPL26, RPL27, RPL27A, RPL28, RPL29, RPL30, RPL31, RPL32, RPL35, RPL35A, RPL36, RPL3L, RPL4, RPL5, RPL6, RPL7, RPL7A, RPL8, RPL9, RPLP0, RPLP2, RPN1, RPN2, RPP38-DT, RPRM, RPRML, RPS10, RPS11, RPS12, RPS13, RPS14, RPS15, RPS15A, RPS16, RPS17, RPS18, RPS19, RPS2, RPS20, RPS23, RPS24, RPS26, RPS27A, RPS3, RPS4X, RPS4Y1, RPS5, RPS6, RPS6KC1, RPS7, RPS8, RPS9, RPSA, RRAS2, RRBP1, RRH, RRM1, RRM2B, RSL1D1, RTL1, RTP3, RTP4, RTP5, RTTN, RUFY3, RUSF1, RUVBL1, RUVBL2, RXFP3, RYK, RYR1, RYR2, RYR3, S100A10, S1PR5, SACM1L, SAG, SAMD5, SAMD8, SAMM50, SASH1, SAT1, SBF1, SBF2, SC5D, SCAI, SCAMP1, SCAMP2, SCAMP3, SCAMP4, SCAMP5, SCAP, SCARB1, SCARB2, SCARF1, SCARF2, SCART1, SCCPDH, SCD, SCD5, SCFD1, SCIMP, SCN11A, SCN1A, SCN2A, SCN2B, SCN3A, SCN3B, SCN4A, SCN4B, SCN5A, SCN7A, SCN8A, SCN9A, SCNN1A, SCNN1B, SCNN1D, SCOC, SCP2, SCRIB, SCYL1, SDC1, SDC2, SDC3, SDC4, SDCBP, SDF2L1, SDF4, SDHC, SDIM1, SDK1, SDK2, SDR42E1, SEC11B, SEC11C, SEC22B, SEC22C, SEC61A1, SEC61A2, SEC61B, SEC61G, SEC62, SEC63, SECTM1, SEL1L, SEL1L3, SELENBP1, SELENOI, SELENOK, SELENOP, SELENOT, SELPLG, SEMA3D, SEMA4B, SEMA4C, SEMA4D, SEMA4F, SEMA5A, SEMA5B, SEMA6A, SEMA6B, SEMA6D, SEMA7A, SERAC1, SERBP1, SERF1A, SERF1B, SERINC1, SERINC2, SERINC3, SERINC4, SERINC5, SERP1, SERP2, SERPINA11, SERPINA5, SERPINA9, SERPINB1, SERPINB13, SERPINB6, SERPINB9, SERTM1, SERTM2, SEZ6, SEZ6L, SEZ6L2, SFT2D1, SFT2D2, SFT2D3, SFTPC, SFXN1, SFXN2, SFXN3, SFXN4, SFXN5, SGCA, SGIP1, SGMS1, SGMS2, SGPL1, SGPP2, SGTA, SGTB, SH2B1, SH3BP4, SH3GL2, SH3GLB1, SH3GLB2, SH3KBP1, SHANK1, SHANK2, SHISA4, SHISA5, SHISA6, SHISA7, SHISA8, SHISAL1, SHISAL2A, SHISAL2B, SI, SIDT1, SIDT2, SIGIRR, SIGLEC1, SIGLEC10, SIGLEC12, SIGLEC15, SIGLEC16, SIGLEC6, SIGLEC7, SIGLEC8, SIGLEC9, SIGLECL1, SIGMAR1, SIRPA, SIRPB1, SIRPB2, SIRPG, SLAMF7, SLAMF8, SLC10A1, SLC10A3, SLC10A5, SLC10A6, SLC11A2, SLC12A1, SLC12A2, SLC12A3, SLC12A4, SLC12A5, SLC12A6, SLC12A7, SLC12A8, SLC12A9, SLC13A1, SLC13A2, SLC13A3, SLC13A4, SLC13A5, SLC14A2, SLC15A1, SLC15A2, SLC15A3, SLC15A4, SLC15A5, SLC16A1, SLC16A10, SLC16A11, SLC16A14, SLC16A2, SLC16A3, SLC16A4, SLC16A5, SLC16A6, SLC16A7, SLC16A8, SLC17A1, SLC17A2, SLC17A3, SLC17A4, SLC17A5, SLC17A7, SLC17A9, SLC18A1, SLC18A2, SLC19A1, SLC19A2, SLC19A3, SLC19A4P, SLC1A1, SLC1A2, SLC1A3, SLC1A4, SLC1A5, SLC1A6, SLC1A7, SLC20A1, SLC20A2, SLC22A1, SLC22A10, SLC22A11, SLC22A12, SLC22A13, SLC22A14, SLC22A15, SLC22A16, SLC22A18, SLC22A2, SLC22A20P, SLC22A23, SLC22A25, SLC22A3, SLC22A31, SLC22A4, SLC22A5, SLC22A6, SLC22A7, SLC23A1, SLC23A2, SLC23A3, SLC24A1, SLC24A4, SLC24A5, SLC25A1, SLC25A10, SLC25A11, SLC25A12, SLC25A14, SLC25A15, SLC25A16, SLC25A17, SLC25A19, SLC25A20, SLC25A23, SLC25A24, SLC25A25, SLC25A26, SLC25A27, SLC25A29, SLC25A3, SLC25A31, SLC25A32, SLC25A37, SLC25A38, SLC25A4, SLC25A44, SLC25A45, SLC25A48, SLC25A5, SLC25A52, SLC25A6, SLC26A1, SLC26A10P, SLC26A11, SLC26A2, SLC26A3, SLC26A4, SLC26A5, SLC26A6, SLC26A7, SLC26A8, SLC27A1, SLC27A2, SLC27A3, SLC27A4, SLC28A2, SLC29A1, SLC29A3, SLC29A4, SLC2A1, SLC2A10, SLC2A11, SLC2A12, SLC2A13, SLC2A14, SLC2A2, SLC2A3, SLC2A4, SLC2A6, SLC2A8, SLC2A9, SLC30A1, SLC30A10, SLC30A5, SLC30A6, SLC31A1, SLC31A2, SLC33A1, SLC34A2, SLC35A1, SLC35A5, SLC35B1, SLC35B2, SLC35B3, SLC35B4, SLC35C1, SLC35C2, SLC35D2, SLC35E1, SLC35E2A, SLC35E2B, SLC35E3, SLC35E4, SLC35F2, SLC35F3, SLC35F4, SLC35F5, SLC35F6, SLC35G3, SLC35G4, SLC35G5, SLC35G6, SLC36A1, SLC36A2, SLC36A3, SLC36A4, SLC37A1, SLC37A2, SLC37A3, SLC37A4, SLC38A1, SLC38A10, SLC38A11, SLC38A3, SLC38A4, SLC38A5, SLC38A6, SLC38A7, SLC38A8, SLC39A1, SLC39A11, SLC39A12, SLC39A13, SLC39A14, SLC39A5, SLC39A7, SLC39A8, SLC3A1, SLC3A2, SLC40A1, SLC41A1, SLC41A2, SLC41A3, SLC43A3, SLC44A1, SLC44A2, SLC44A3, SLC44A4, SLC44A5, SLC45A1, SLC45A2, SLC45A3, SLC45A4, SLC46A1, SLC46A2, SLC47A1, SLC47A2, SLC48A1, SLC49A3, SLC49A4, SLC4A1, SLC4A10, SLC4A11, SLC4A2, SLC4A3, SLC4A4, SLC4A5, SLC4A7, SLC4A8, SLC50A1, SLC51A, SLC51B, SLC5A11, SLC5A2, SLC5A3, SLC5A5, SLC5A6, SLC5A7, SLC5A9, SLC66A1, SLC66A2, SLC66A3, SLC6A1, SLC6A11, SLC6A12, SLC6A13, SLC6A14, SLC6A15, SLC6A16, SLC6A17, SLC6A18, SLC6A19, SLC6A2, SLC6A20, SLC6A3, SLC6A4, SLC6A5, SLC6A6, SLC6A7, SLC6A8, SLC6A9, SLC7A1, SLC7A10, SLC7A11, SLC7A4, SLC7A5, SLC7A5P1, SLC7A5P2, SLC7A6, SLC7A7, SLC7A8, SLC8A1, SLC8A2, SLC8A3, SLC8B1, SLC9A1, SLC9A2, SLC9A5, SLC9A7, SLC9A9, SLC9B1, SLC9B1P1, SLC9B2, SLC9C1, SLCO1A2, SLCO1B1, SLCO1B3, SLCO2A1, SLCO2B1, SLCO3A1, SLCO4A1, SLCO5A1, SLCO6A1, SLFN12L, SLFN5, SLIT2, SLITRK1, SLITRK2, SLITRK3, SLITRK4, SLITRK5, SLMAP, SLN, SLU7, SMAD1, SMAD2, SMAD6, SMARCA4, SMCHD1, SMCO1, SMCO2, SMCO3, SMCO4, SMIM1, SMIM10, SMIM11, SMIM12, SMIM13, SMIM14, SMIM15, SMIM17, SMIM18, SMIM19, SMIM2, SMIM20, SMIM21, SMIM22, SMIM24, SMIM26, SMIM27, SMIM28, SMIM29, SMIM3, SMIM31, SMIM32, SMIM33, SMIM34, SMIM35, SMIM36, SMIM38, SMIM39, SMIM40, SMIM41, SMIM42, SMIM44, SMIM45, SMIM46, SMIM47, SMIM5, SMIM6, SMIM7, SMIM8, SMLR1, SMPD1, SMPD3, SMPD4, SMPX, SMURF2, SMYD3, SNAP23, SNAP25, SNAP47, SNAP91, SNAPIN, SNCA, SND1, SNF8, SNN, SNORC, SNPH, SNRNP200, SNRNP40, SNTA1, SNTB2, SNX1, SNX10, SNX11, SNX12, SNX13, SNX14, SNX15, SNX17, SNX2, SNX21, SNX24, SNX25, SNX27, SNX30, SNX33, SNX4, SNX8, SNX9, SOAT1, SOAT2, SORCS1, SORCS2, SORCS3, SORD, SORL1, SORT1, SPA17, SPACA4, SPACA6, SPAG4, SPAG8, SPAG9, SPAST, SPATA25, SPATA3, SPATA31A1, SPATA31A3, SPATA31A5, SPATA31A6, SPATA31A7, SPATA31C1, SPATA31C2, SPATA31D1, SPATA31D3, SPATA31D4, SPATA31E1, SPATA31F1, SPATA31F3, SPATA9, SPECC1, SPEM1, SPEM2, SPEM3, SPG21, SPG7, SPHK1, SPHK2, SPI1, SPIN1, SPIN3, SPINT1, SPINT2, SPN, SPNS1, SPNS2, SPNS3, SPPL2A, SPPL2B, SPPL2C, SPPL3, SPRED3, SPRY1, SPRY2, SPRY3, SPRY4, SPTAN1, SPTB, SPTBN1, SPTBN4, SPTBN5, SPTLC1, SPTLC2, SPTLC3, SQLE, SRD5A1, SRI, SRPRA, SRPRB, SRPX, SSBP4, SSC4D, SSC5D, SSH1, SSMEM1, SSPN, SSR1, SSR2, ST14, ST3GAL1, ST3GAL2, ST3GAL3, ST3GAL4, ST3GAL5, ST3GAL6, ST6GAL2, ST6GALNAC1, ST6GALNAC4, ST6GALNAC5, ST6GALNAC6, ST7, ST7L, ST8SIA1, ST8SIA3, ST8SIA6, STAB1, STAG1, STAG2, STAMBP, STAMBPL1, STARD10, STARD13, STARD3, STARD3NL, STAU1, STAU2, STBD1, STEAP1, STEAP1B, STEAP4, STIM1, STIM2, STIMATE, STIMATE-MUSTN1, STK11, STK16, STK26, STK38L, STMN1, STMN2, STN1, STOM, STOML1, STOML2, STON1, STON2, STRA6, STRADB, STRN, STRN3, STS, STT3A, STT3B, STUM, STX10, STX11, STX12, STX16, STX16-NPEPL1, STX17, STX18, STX1B, STX2, STX3, STX4, STX5, STX8, STXBP1, STXBP5L, STXBP6, STYK1, SUCO, SUN1, SUN2, SUN3, SUN5, SURF1, SUSD1, SUSD3, SUSD4, SUSD5, SUSD6, SV2B, SVEP1, SVIP, SVOP, SVOPL, SYAP1, SYBU, SYCE1, SYNCRIP, SYNDIG1L, SYNE1, SYNE3, SYNGR1, SYNGR2, SYNGR3, SYNGR4, SYNJ2BP-COX16, SYNPR, SYP, SYPL1, SYPL2, SYT1, SYT10, SYT12, SYT13, SYT14, SYT15, SYT15B, SYT16, SYT17, SYT3, SYT4, SYT5, SYT6, SYT7, SYT8, SYT9, SYTL1, SYTL2, SYTL4, SYTL5, SYVN1, TAB2, TACC1, TACSTD2, TAFA5, TAFAZZIN, TANGO6, TAOK2, TAP1, TAP2, TAPBP, TAPT1, TARM1, TARP, TAS1R1, TAS1R2, TAS1R3, TAS2R1, TAS2R10, TAS2R13, TAS2R14, TAS2R16, TAS2R19, TAS2R20, TAS2R3, TAS2R30, TAS2R31, TAS2R33, TAS2R36, TAS2R38, TAS2R39, TAS2R4, TAS2R40, TAS2R41, TAS2R42, TAS2R43, TAS2R45, TAS2R46, TAS2R5, TAS2R50, TAS2R60, TAS2R7, TAS2R8, TAS2R9, TBC1D10C, TBC1D13, TBC1D20, TBC1D7, TBC1D8, TBC1D9B, TBL1XR1, TBXAS1, TCIRG1, TCP11, TCTA, TCTN1, TCTN2, TCTN3, TDRKH, TECR, TECRL, TECTA, TEDDM1, TELO2, TENM2, TENM3, TENM4, TESC, TEX2, TEX261, TEX28, TEX28P2, TEX29, TEX38, TEX46, TEX50, TEX51, TFCP2L1, TFR2, TFRC, TGFA, TGFBR1, TGFBR2, TGFBRAP1, TGM1, TGM4, TGOLN2, THADA, THOC3, THSD7B, TIAM2, TIGIT, TIMD4, TIMM50, TIMMDC1, TIRAP, TJAP1, TLCD1, TLCD3B, TLCD4, TLCD4-RWDD3, TLCD5, TLL1, TLR1, TLR10, TLR2, TLR3, TLR4, TLR5, TLR6, TLR7, TLR8, TLR9, TM2D1, TM2D2, TM2D3, TM4SF1, TM4SF18, TM4SF19, TM4SF20, TM4SF4, TM4SF5, TM6SF1, TM7SF2, TM7SF3, TM9SF1, TM9SF2, TM9SF3, TM9SF4, TMBIM1, TMBIM4, TMBIM6, TMC1, TMC2, TMC3, TMC4, TMC5, TMC6, TMC7, TMC8, TMCC1, TMCC2, TMCC3, TMCO1, TMCO2, TMCO3, TMCO4, TMCO5A, TMCO5B, TMCO6, TMDD1, TMED1, TMED10, TMED2, TMED3, TMED4, TMED5, TMED7, TMED7-TICAM2, TMEFF2, TMEM100, TMEM101, TMEM104, TMEM105, TMEM106A, TMEM106C, TMEM107, TMEM108, TMEM114, TMEM116, TMEM117, TMEM119, TMEM120A, TMEM121, TMEM123, TMEM125, TMEM126A, TMEM126B, TMEM127, TMEM128, TMEM129, TMEM130, TMEM131, TMEM131L, TMEM132A, TMEM132B, TMEM132C, TMEM132D, TMEM132E, TMEM134, TMEM139, TMEM140, TMEM141, TMEM143, TMEM144, TMEM145, TMEM147, TMEM14A, TMEM14B, TMEM14DP, TMEM14EP, TMEM150B, TMEM150C, TMEM151A, TMEM151B, TMEM154, TMEM156, TMEM158, TMEM161A, TMEM161B, TMEM164, TMEM165, TMEM169, TMEM171, TMEM175, TMEM176A, TMEM177, TMEM178B, TMEM179, TMEM179B, TMEM181, TMEM183A, TMEM183BP, TMEM184A, TMEM184B, TMEM184C, TMEM185A, TMEM185B, TMEM187, TMEM19, TMEM190, TMEM191A, TMEM191B, TMEM191C, TMEM192, TMEM196, TMEM198, TMEM200A, TMEM200B, TMEM200C, TMEM202, TMEM205, TMEM207, TMEM209, TMEM210, TMEM212, TMEM213, TMEM215, TMEM216, TMEM217, TMEM217B, TMEM218, TMEM219, TMEM220, TMEM221, TMEM222, TMEM223, TMEM225, TMEM225B, TMEM229A, TMEM229B, TMEM230, TMEM232, TMEM233, TMEM234, TMEM235, TMEM236, TMEM237, TMEM238, TMEM239, TMEM240, TMEM241, TMEM243, TMEM244, TMEM245, TMEM247, TMEM248, TMEM249, TMEM25, TMEM250, TMEM252, TMEM253, TMEM254, TMEM255A, TMEM255B, TMEM256, TMEM256-PLSCR3, TMEM258, TMEM259, TMEM26, TMEM260, TMEM262, TMEM263, TMEM265, TMEM267, TMEM269, TMEM270, TMEM271, TMEM272, TMEM273, TMEM275, TMEM276, TMEM30A, TMEM30CP, TMEM31, TMEM33, TMEM35B, TMEM37, TMEM39A, TMEM39B, TMEM40, TMEM41A, TMEM41B, TMEM42, TMEM43, TMEM44, TMEM45A, TMEM47, TMEM50A, TMEM51, TMEM52, TMEM52B, TMEM53, TMEM54, TMEM59L, TMEM60, TMEM61, TMEM62, TMEM63A, TMEM63B, TMEM63C, TMEM64, TMEM65, TMEM67, TMEM68, TMEM69, TMEM71, TMEM72, TMEM74B, TMEM78, TMEM79, TMEM80, TMEM81, TMEM82, TMEM86A, TMEM86B, TMEM87A, TMEM87B, TMEM88, TMEM88B, TMEM89, TMEM9, TMEM91, TMEM92, TMEM94, TMEM97, TMEM9B, TMIE, TMIGD2, TMIGD3, TMOD1, TMPO, TMPPE, TMPRSS11A, TMPRSS11E, TMPRSS11F, TMPRSS12, TMPRSS13, TMPRSS15, TMPRSS2, TMPRSS3, TMPRSS4, TMPRSS5, TMPRSS6, TMPRSS9, TMT1A, TMTC1, TMTC2, TMTC3, TMTC4, TMUB1, TMUB2, TMX1, TMX2, TMX4, TNC, TNFRSF10A, TNFRSF10B, TNFRSF10C, TNFRSF10D, TNFRSF13C, TNFRSF14, TNFRSF17, TNFRSF19, TNFRSF1A, TNFRSF1B, TNFRSF25, TNFRSF4, TNFRSF9, TNFSF10, TNFSF11, TNFSF12, TNFSF12-TNFSF13, TNFSF13, TNFSF13B, TNFSF15, TNFSF4, TNFSF8, TNFSF9, TNK1, TNK2, TNMD, TOM1, TOM1L1, TOM1L2, TOMM22, TOMM34, TOMM40, TOMM70, TOR1A, TOR1AIP2, TOR4A, TP53, TP53I11, TP53I13, TPBGL, TPCN1, TPCN2, TPM1, TPM4, TPO, TPRA1, TPSG1, TPST1, TPTE, TPTE2, TRA, TRABD2A, TRAC, TRAF3IP2, TRAM1, TRAM2, TRAP1, TRARG1, TRB, TRBC1, TRBC2, TRDN, TREH, TREM2, TREML1, TREX1, TRGC1, TRGC2, TRHDE, TRIL, TRPA1, TRPC1, TRPC3, TRPC4, TRPC6, TRPC7, TRPM1, TRPM2, TRPM3, TRPM4, TRPM5, TRPM6, TRPM7, TRPM8, TRPV1, TRPV2, TRPV3, TRPV4, TRPV5, TRPV6, TSBP1, TSC1, TSC2, TSHR, TSNARE1, TSPAN1, TSPAN10, TSPAN11, TSPAN12, TSPAN13, TSPAN14, TSPAN15, TSPAN16, TSPAN17, TSPAN18, TSPAN19, TSPAN2, TSPAN3, TSPAN31, TSPAN32, TSPAN4, TSPAN5, TSPAN6, TSPAN7, TSPAN9, TSPO, TSPO2, TTC3, TTK, TTPAL, TTTY13, TTYH1, TUBA8, TUBD1, TUBGCP2, TUBGCP3, TUBGCP4, TUBGCP6, TUFM, TUNAR, TUSC3, TVP23A, TVP23B, TVP23C, TVP23C-CDRT4, TXLNA, TXNDC15, TXNDC16, TYK2, TYRL, TYRO3, TYROBP, TYSND1, TYW1, TYW1B, UBA6, UBAC2, UBE2J2, UBE2T, UBE2W, UBIAD1, UBL4A, UBQLN2, UBR3, UBR4, UBR5, UBXN6, UBXN8, UFL1, UGCG, UGT1A1, UGT1A10, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT2A1, UGT2A3, UGT2B11, UGT2B15, UGT2B17, UGT2B7, UGT3A1, UGT3A2, UGT8, UMOD, UNC13B, UNC13C, UNC13D, UNC5A, UNC5C, UNC5CL, UNC5D, UNC93A, UNC93B1, UPK1A, UPK1B, UPK3B, UPK3BL1, UPK3BL2, UQCC5, UQCRFS1P1, USE1, USO1, USP19, USP2, USP30, USP9X, UST, UTP18, UTRN, UTS2R, UTY, VAMP2, VAMP3, VAMP4, VAMP7, VAMP8, VASN, VAT1, VCAM1, VCAN, VDAC1, VDAC2, VDAC3, VEGFA, VEGFB, VEGFC, VEGFD, VEZT, VIPR1, VIPR2, VLDLR, VMP1, VNN1, VPS16, VPS26B, VPS33A, VPS35L, VPS39, VPS41, VPS45, VPS50, VPS51, VPS52, VPS53, VPS54, VRK1, VSIG1, VSIG10, VSIG10L, VSIG10L2, VSIG2, VSIG4, VSIG8, VSNL1, VSTM1, VSTM2A, VSTM2B, VSTM2L, VSTM4, VSTM5, VTCN1, VTI1B, WBP1, WBP1L, WDFY3, WDR11, WDR17, WDR59, WDR83OS, WFS1, WLS, WNK1, WNK4, WNT5A, WRNIP1, WWP2, XAB2, XBP1, XCE, XCR1, XG, XK, XKR3, XKR5, XKR6, XKR8, XKR9, XKRX, XKRY, XPNPEP2, XPO1, XRCC5, XRCC6, XRN1, XRN2, XYLT1, YAP1, YIPF2, YIPF5, YIPF6, YIPF7, YKT6, YME1L1, YWHAB, YWHAE, YWHAG, YWHAH-AS1, YWHAQ, ZBED3, ZC3H13, ZDHHC1, ZDHHC11, ZDHHC11B, ZDHHC12, ZDHHC13, ZDHHC14, ZDHHC16, ZDHHC2, ZDHHC20, ZDHHC22, ZDHHC23, ZDHHC24, ZDHHC3, ZDHHC4, ZDHHC5, ZDHHC7, ZFAND2B, ZFP14, ZFPL1, ZMPSTE24, ZMYND11, ZMYND19, ZNF106, ZNF138, ZNF219, ZNF230, ZNF286A, ZNF451, ZNF474, ZNF546, ZNF566, ZNF593OS, ZNF66, ZNF7, ZNF708, ZNF804A, ZNF816, ZNRF1, ZNRF2, ZNRF3, ZPBP, ZW10

ParishinB

3-hydroxy-5-oxo-5-[[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methoxy]-3-[[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methoxycarbonyl]pentanoic acid

C32H40O19 (728.2164)

Parishin B is a glycoside. Parishin B is a natural product found in Artemisia absinthium with data available. Parishin B, a parishin derivative isolated from Gastrodia elata, may have antioxidant property[1]. Parishin B, a parishin derivative isolated from Gastrodia elata, may have antioxidant property[1].

Deltoside

.BETA.-D-GLUCOPYRANOSIDE, (3.BETA.,25R)-26-(.BETA.-D-GLUCOPYRANOSYLOXY)-22-HYDROXYFUROST-5-EN-3-YL O-6-DEOXY-.ALPHA.-L-MANNOPYRANOSYL-(1->2)-O-(.BETA.-D-GLUCOPYRANOSYL-(1->4))-

C51H84O23 (1064.5403)

Deltoside is a steroid saponin. Protodeltonin is a natural product found in Balanites roxburghii, Trigonella foenum-graecum, and Balanites aegyptiaca with data available.

2-Hydroxyadenine

FLUDARABINE PHOSPHATE IMPURITY, ISOGUANINE [USP IMPURITY]

C5H5N5O (151.0494)

2-Hydroxyadenine (2-OH-Ade) is formed by hydroxyl radical attack on DNA bases and shows a genotoxicity in human, being the source of the mutations induced by reactive oxygen species. 2-OH-Ade in DNA is miscoding and elicits various mutations, and is a mutagenic in bacterial and mammalian cells. (Recent Research Developments in Biochemistry (2000)2:41-50) [HMDB] 2-Hydroxyadenine (2-OH-Ade) is formed by hydroxyl radical attack on DNA bases and shows a genotoxicity in human, being the source of the mutations induced by reactive oxygen species. 2-OH-Ade in DNA is miscoding and elicits various mutations, and is a mutagenic in bacterial and mammalian cells. (Recent Research Developments in Biochemistry (2000)2:41-50). Isoguanine is an oxopurine that is 3,7-dihydro-purin-2-one in which the hydrogen at position 6 is substituted by an amino group.

Uvaretin

1- [ 2,4-Dihydroxy-3- [ (2-hydroxyphenyl) methyl ] -6-methoxyphenyl ] -3-phenyl-1-propanone

C23H22O5 (378.1467)

Uvaretin is a member of the class of dihydrochalcones that is 1,3-diphenylpropan-1-one in which the phenyl group that is bonded to the carbonyl group is substituted by hydroxy groups at positions 2 and 4, an o-hydroxybenzyl group at position 3, and a methoxy group at position 6. A cytotoxic natural product found particularly in Uvaria acuminata and Uvaria chamae. It has a role as an antineoplastic agent and a plant metabolite. It is a resorcinol, an aromatic ether, a polyketide and a member of dihydrochalcones. Uvaretin is a natural product found in Desmos chinensis, Uvaria chamae, and other organisms with data available. A member of the class of dihydrochalcones that is 1,3-diphenylpropan-1-one in which the phenyl group that is bonded to the carbonyl group is substituted by hydroxy groups at positions 2 and 4, an o-hydroxybenzyl group at position 3, and a methoxy group at position 6. A cytotoxic natural product found particularly in Uvaria acuminata and Uvaria chamae.

Melilotoside

(2E)-3-(2-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoic acid

C15H18O8 (326.1002)

Melilotoside, also known as trans-beta-D-glucosyl-2-hydroxycinnamic acid or beta-D-glucosyl-2-coumarate, belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans and flavonoids. Melilotoside is an extremely weak basic (essentially neutral) compound (based on its pKa). Melilotoside is found in herbs and spices. Melilotoside has been isolated from Melilotus alba (white melilot), Melilotus altissimus (tall yellow sweet clover), and other plants. Trans-beta-D-glucosyl-2-hydroxycinnamic acid is a glucosyl hydroxycinnamic acid. It is a conjugate acid of a trans-beta-D-glucosyl-2-hydroxycinnamate. Melilotoside is a natural product found in Mikania laevigata, Serpocaulon triseriale, and other organisms with data available.

Fargesone A

(2S,3R,3aR,7S,7aS)-2-(1,3-benzodioxol-5-yl)-3a,4-dimethoxy-3-methyl-7-prop-2-enyl-2,3,7,7a-tetrahydro-1-benzofuran-6-one

C21H24O6 (372.1573)

Fargesone A is a member of benzodioxoles. Fargesone A is a natural product found in Piper wightii, Piper hymenophyllum, and other organisms with data available.

Trispherine

(2S,3S,9S,10S)-9-hydroxy-4-methyl-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),7,13,15(19)-tetraen-12-one

C17H17NO5 (315.1107)

4-Isopropylbenzoic acid

InChI=1/C10H12O2/c1-7(2)8-3-5-9(6-4-8)10(11)12/h3-7H,1-2H3,(H,11,12

C10H12O2 (164.0837)

P-cumic acid is a cumic acid that consists of benzoic acid substituted by an isopropyl group at position 4. It has a role as a plant metabolite. It is a conjugate acid of a p-cumate. 4-Isopropylbenzoic acid is a natural product found in Libocedrus yateensis, Bridelia retusa, and other organisms with data available. Constituent of various plant subspecies including Cuminum cyminum (cumin), Ferula subspecies and Perilla frutescens (perilla). 4-Isopropylbenzoic acid is found in cumin, fats and oils, and herbs and spices. 4-Isopropylbenzoic acid is found in cumin. 4-Isopropylbenzoic acid is a constituent of various plant species including Cuminum cyminum (cumin), Ferula species and Perilla frutescens (perilla). A cumic acid that consists of benzoic acid substituted by an isopropyl group at position 4. KEIO_ID C157 4-Isopropylbenzoic acid, an aromatic monoterpenoid, is isolated from the stem bark of Bridelia retusa. 4-Isopropylbenzoic acid exhibits antifungal activities. 4-Isopropylbenzoic acid is also a reversible and uncompetitive inhibitor of mushroom tyrosinase[1][2]. 4-Isopropylbenzoic acid, an aromatic monoterpenoid, is isolated from the stem bark of Bridelia retusa. 4-Isopropylbenzoic acid exhibits antifungal activities. 4-Isopropylbenzoic acid is also a reversible and uncompetitive inhibitor of mushroom tyrosinase[1][2].

Docosanedioic acid

1,20-Eicosanedicarboxylic acid

C22H42O4 (370.3083)

Phellogenic acid, also known as 1,20-eicosanedicarboxylic acid or 1,22-docosanedioate, is a member of the class of compounds known as very long-chain fatty acids. Very long-chain fatty acids are fatty acids with an aliphatic tail that contains at least 22 carbon atoms. Thus, phellogenic acid is considered to be a fatty acid lipid molecule. Phellogenic acid is practically insoluble (in water) and a weakly acidic compound (based on its pKa). Phellogenic acid can be found in potato, which makes phellogenic acid a potential biomarker for the consumption of this food product. Docosanedioic acid is an alpha,omega-dicarboxylic acid that is docosane in which the methyl groups have been oxidised to the corresponding carboxylic acids. It has a role as a metabolite. It is an alpha,omega-dicarboxylic acid and a dicarboxylic fatty acid. It is a conjugate acid of a docosanedioate(2-). It derives from a hydride of a docosane. Docosanedioic acid is a natural product found in Pinus radiata with data available.

Asparagine

(2S)-2-Amino-3-carbamoylpropanoic acid

C4H8N2O3 (132.0535)

Asparagine (Asn) or L-asparagine is an alpha-amino acid. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). Amino acids are organic compounds that contain amino (‚ÄìNH2) and carboxyl (‚ÄìCOOH) functional groups, along with a side chain (R group) specific to each amino acid. L-asparagine is one of 20 proteinogenic amino acids, i.e., the amino acids used in the biosynthesis of proteins. Asparagine is found in all organisms ranging from bacteria to plants to animals. In humans, asparagine is not an essential amino acid, which means that it can be synthesized from central metabolic pathway intermediates in humans and is not required in the diet. The precursor to asparagine is oxaloacetate. Oxaloacetate is converted to aspartate using a transaminase enzyme. This enzyme transfers the amino group from glutamate to oxaloacetate producing alpha-ketoglutarate and aspartate. The enzyme asparagine synthetase produces asparagine, AMP, glutamate, and pyrophosphate from aspartate, glutamine, and ATP. In the asparagine synthetase reaction, ATP is used to activate aspartate, forming beta-aspartyl-AMP. Glutamine donates an ammonium group which reacts with beta-aspartyl-AMP to form asparagine and free AMP. Since the asparagine side chain can make efficient hydrogen bond interactions with the peptide backbone, asparagines are often found near the beginning and end of alpha-helices, and in turn motifs in beta sheets. Its role can be thought as "capping" the hydrogen bond interactions which would otherwise need to be satisfied by the polypeptide backbone. Asparagine also provides key sites for N-linked glycosylation, a modification of the protein chain that is characterized by the addition of carbohydrate chains. A reaction between asparagine and reducing sugars or reactive carbonyls produces acrylamide (acrylic amide) in food when heated to sufficient temperature (i.e. baking). These occur primarily in baked goods such as French fries, potato chips, and roasted coffee. Asparagine was first isolated in 1806 from asparagus juice --hence its name. Asparagine was the first amino acid to be isolated. The smell observed in the urine of some individuals after the consumption of asparagus is attributed to a byproduct of the metabolic breakdown of asparagine, asparagine-amino-succinic-acid monoamide. However, some scientists disagree and implicate other substances in the smell, especially methanethiol. [Spectral] L-Asparagine (exact mass = 132.05349) and L-Aspartate (exact mass = 133.03751) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions. One of the nonessential amino acids. Dietary supplement, nutrient. Widely distributed in the plant kingdom. Isolated from asparagus, beetroot, peas, beans, etc. (-)-Asparagine. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=70-47-3 (retrieved 2024-07-15) (CAS RN: 70-47-3). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). L-Asparagine ((-)-Asparagine) is a non-essential amino acid that is involved in the metabolic control of cell functions in nerve and brain tissue. L-Asparagine ((-)-Asparagine) is a non-essential amino acid that is involved in the metabolic control of cell functions in nerve and brain tissue.

2,6-DICHLOROBENZAMIDE

C7H5Cl2NO (188.9748)

A member of the class of benzamides that is benzamide substituted by chloro groups at positions 2 and 6. CONFIDENCE standard compound; EAWAG_UCHEM_ID 85 CONFIDENCE standard compound; INTERNAL_ID 3374 CONFIDENCE standard compound; INTERNAL_ID 4051 CONFIDENCE standard compound; INTERNAL_ID 8429

dIMP

[(2R,3S,4R,5R)-3-Hydroxy-5-(6-hydroxy-9H-purin-9-yl)tetrahydrofuran-2-yl]methyl dihydrogen phosphate

C10H13N4O7P (332.0522)

dIMP is a deoxyribonucleoside and is considered a derivative of the nucleoside inosine, differing from the latter by the replacement of a hydroxyl group (-OH) by hydrogen (-H) at the 2 position of its ribose sugar moiety. The hydrolytic deamination of dAMP residues in DNA yields dIMP residues. The deamination of adenine residues in DNA generates hypoxanthine, which is mutagenic since it can pair not only with thymine but also with cytosine and therefore would result in A-T to G-C transitions after DNA replication. Hypoxanthine DNA glycosylase (EC 3.2.2.15) excises hypoxanthine from DNA containing dIMP residues in mammalian cells. (PMID: 10684927, 8016081) [HMDB] dIMP is a deoxyribonucleoside and is considered a derivative of the nucleoside inosine, differing from the latter by the replacement of a hydroxyl group (-OH) by hydrogen (-H) at the 2 position of its ribose sugar moiety. The hydrolytic deamination of dAMP residues in DNA yields dIMP residues. The deamination of adenine residues in DNA generates hypoxanthine, which is mutagenic since it can pair not only with thymine but also with cytosine and therefore would result in A-T to G-C transitions after DNA replication. Hypoxanthine DNA glycosylase (EC 3.2.2.15) excises hypoxanthine from DNA containing dIMP residues in mammalian cells. (PMID: 10684927, 8016081). Acquisition and generation of the data is financially supported in part by CREST/JST. COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

BENSULIDE

O,O-bis(propan-2-yl) [(2-benzenesulfonamidoethyl)sulfanyl]phosphonothioate

C14H24NO4PS3 (397.0605)

CONFIDENCE standard compound; INTERNAL_ID 1379; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4596; ORIGINAL_PRECURSOR_SCAN_NO 4592 CONFIDENCE standard compound; INTERNAL_ID 1379; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9469; ORIGINAL_PRECURSOR_SCAN_NO 9465 CONFIDENCE standard compound; INTERNAL_ID 1379; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9501; ORIGINAL_PRECURSOR_SCAN_NO 9497 CONFIDENCE standard compound; INTERNAL_ID 1379; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9475; ORIGINAL_PRECURSOR_SCAN_NO 9473 CONFIDENCE standard compound; INTERNAL_ID 1379; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4616; ORIGINAL_PRECURSOR_SCAN_NO 4612 CONFIDENCE standard compound; INTERNAL_ID 1379; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9463; ORIGINAL_PRECURSOR_SCAN_NO 9460 CONFIDENCE standard compound; INTERNAL_ID 1379; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4614; ORIGINAL_PRECURSOR_SCAN_NO 4610 CONFIDENCE standard compound; INTERNAL_ID 1379; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9468; ORIGINAL_PRECURSOR_SCAN_NO 9465 CONFIDENCE standard compound; INTERNAL_ID 1379; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9473; ORIGINAL_PRECURSOR_SCAN_NO 9472 CONFIDENCE standard compound; INTERNAL_ID 1379; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4602; ORIGINAL_PRECURSOR_SCAN_NO 4600 CONFIDENCE standard compound; INTERNAL_ID 1379; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4602; ORIGINAL_PRECURSOR_SCAN_NO 4597 CONFIDENCE standard compound; INTERNAL_ID 1379; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4592; ORIGINAL_PRECURSOR_SCAN_NO 4587

zectran

Pesticide9_Mexacarbate_C12H18N2O2_4-(Dimethylamino)-3,5-dimethylphenyl methylcarbamate

C12H18N2O2 (222.1368)

C471 - Enzyme Inhibitor > C47792 - Acetylcholinesterase Inhibitor

Benzoyl ecgonine

(1R,2R,3S,5S)-8-Methyl-3-[(phenylcarbonyl)oxy]-8-azabicyclo[3.2.1]octane-2-carboxylic acid

C16H19NO4 (289.1314)

Benzoylecgonine is the major metabolite of cocaine. It is formed by hydrolysis of cocaine in the liver, catalysed by carboxylesterases. It is excreted in the urine of cocaine users after processing in the liver. [Wikipedia] CONFIDENCE standard compound; INTERNAL_ID 1590

Diisopropylphthalate

DIISOPROPYL PHTHALATE

C14H18O4 (250.1205)

CONFIDENCE standard compound; INTERNAL_ID 832; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9433; ORIGINAL_PRECURSOR_SCAN_NO 9428 CONFIDENCE standard compound; INTERNAL_ID 832; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4533; ORIGINAL_PRECURSOR_SCAN_NO 4530 CONFIDENCE standard compound; INTERNAL_ID 832; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9448; ORIGINAL_PRECURSOR_SCAN_NO 9444 CONFIDENCE standard compound; INTERNAL_ID 832; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4512; ORIGINAL_PRECURSOR_SCAN_NO 4510 CONFIDENCE standard compound; INTERNAL_ID 832; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9411; ORIGINAL_PRECURSOR_SCAN_NO 9407 CONFIDENCE standard compound; INTERNAL_ID 832; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9458; ORIGINAL_PRECURSOR_SCAN_NO 9456 CONFIDENCE standard compound; INTERNAL_ID 832; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4596; ORIGINAL_PRECURSOR_SCAN_NO 4593 CONFIDENCE standard compound; INTERNAL_ID 832; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9380; ORIGINAL_PRECURSOR_SCAN_NO 9378 CONFIDENCE standard compound; INTERNAL_ID 832; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4515; ORIGINAL_PRECURSOR_SCAN_NO 4513 CONFIDENCE standard compound; INTERNAL_ID 832; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9407; ORIGINAL_PRECURSOR_SCAN_NO 9402 CONFIDENCE standard compound; INTERNAL_ID 832; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4506; ORIGINAL_PRECURSOR_SCAN_NO 4505 CONFIDENCE standard compound; INTERNAL_ID 832; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4506; ORIGINAL_PRECURSOR_SCAN_NO 4504 CONFIDENCE standard compound; INTERNAL_ID 196

N-Acetylanthranilate

2-(Acetylamino)-benzoic acid

C9H9NO3 (179.0582)

11beta-Hydroxyetiocholanolone

3alpha,11beta-Dihydroxy-5beta-androstane-17-one

C19H30O3 (306.2195)

D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones

Tomatidine

5,7,9,13-tetramethyl-5-oxaspiro[pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosane-6,2-piperidine]-16-ol

C27H45NO2 (415.345)

Tomatidine is the aglycone derivative of tomatine. Tomatidine belongs to the chemical family known as Spirosolanes and Derivatives. These are steroidal alkaloids whose structure contains a spirosolane skeleton. Tomatine (the glycosylated form of tomatidine) is a mildly toxic glycoalkaloid or glycospirosolane found in the stems and leaves of tomato plants as well as in the fruit of unripened (green) tomatoes (up to 500 mg/kg). Red, ripe tomatoes have somewhat reduced amounts of tomatine and tomatidine. Both tomatine and tomatidine possess antimicrobial, antifungal and antiviral properties. Tomatidine has been shown to exhibit anti-virulence activity against normal strains of Staphylococcus aureus as well as the ability to potentiate the effect of aminoglycoside antibiotics (PMID: 24877760). Recent studies have shown that tomatidine stimulates mTORC1 signaling and anabolism, leading to accumulation of protein and mitochondria, and ultimately, cell growth. Furthermore, in mice, tomatidine has been shown to increase skeletal muscle mTORC1 signaling, reduce skeletal muscle atrophy, enhance recovery from skeletal muscle atrophy, stimulate skeletal muscle hypertrophy, and increase strength and exercise capacity (PMID: 24719321). Tomatidine has also been shown to significantly inhibit cholesterol ester accumulation induced by acetylated LDL in human monocyte-derived macrophages in a dose-dependent manner. Tomatidine also inhibits cholesterol ester formation in Chinese hamster ovary cells overexpressing acyl-CoA:cholesterol acyl-transferase (ACAT)-1 or ACAT-2, suggesting that tomatidine suppresses both ACAT-1 and ACAT-2 activities. The oral administration of tomatidine to apoE-deficient mice significantly reduces levels of serum cholesterol, LDL-cholesterol, and the size of atherosclerotic lesions (PMID: 22224814). Alkaloid from Lycopersicon esculentum (tomato). Tomatidine is found in garden tomato, garden tomato (variety), and potato. Tomatidine acts as an anti-inflammatory agent by blocking NF-κB and JNK signaling[1]. Tomatidine activates autophagy either in mammal cells or C elegans[2]. Tomatidine acts as an anti-inflammatory agent by blocking NF-κB and JNK signaling[1]. Tomatidine activates autophagy either in mammal cells or C elegans[2].

3-Acetylmorphine

O(3)-Monoacetylmorphine

C19H21NO4 (327.1471)

D002492 - Central Nervous System Depressants > D009294 - Narcotics > D053610 - Opiate Alkaloids

Docosatrienoate (22:3n3)

(13E,16E,19E)-Docosa-13,16,19-trienoic acid

C22H38O2 (334.2872)

Docosatrienoic acid, also known as docosatrienoate, belongs to the class of organic compounds known as very long-chain fatty acids. These are fatty acids with an aliphatic tail that contains at least 22 carbon atoms. Docosatrienoic acid is a very hydrophobic molecule, is practically insoluble (in water), and is relatively neutral. Application of docosatrienoic acid was shown to dose-dependently decrease the peak K+ current amplitude and accelerate the potassium activation and inactivation kinetics at all membrane potentials.

2,4-DMA

2,4-Dimethylaniline

C8H11N (121.0891)

KEIO_ID D180

D-Chicoric acid

(2S,3S)-2,3-Bis[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]butanedioic acid

C22H18O12 (474.0798)

D-Chicoric acid is found in green vegetables. D-Chicoric acid is isolated from chicory (Cichorium intybus) and Cichorium endivia (endive). Isolated from chicory (Cichorium intybus) and Cichorium endivia (endive). D-Chicoric acid is found in green vegetables. Chicoric acid (Cichoric acid), an orally active dicaffeyltartaric acid, induces reactive oxygen species (ROS) generation. Chicoric acid inhibits cell viability and induces mitochondria-dependent apoptosis in 3T3-L1 preadipocytes through ROS-mediated PI3K/Akt and MAPK signaling pathways. Chicoric acid increases glucose uptake, improves insulin resistance, and attenuates glucosamine-induced inflammation. Chicoric acid has antidiabetic properties and antioxidant, anti-inflammatory effects[1][2][3]. Chicoric acid (Cichoric acid), an orally active dicaffeyltartaric acid, induces reactive oxygen species (ROS) generation. Chicoric acid inhibits cell viability and induces mitochondria-dependent apoptosis in 3T3-L1 preadipocytes through ROS-mediated PI3K/Akt and MAPK signaling pathways. Chicoric acid increases glucose uptake, improves insulin resistance, and attenuates glucosamine-induced inflammation. Chicoric acid has antidiabetic properties and antioxidant, anti-inflammatory effects[1][2][3]. L-Chicoric Acid ((-)-Chicoric acid) is a dicaffeoyltartaric acid and a potent, selective and reversible HIV-1 integrase inhibitor with an IC50 of ~100 nM. L-Chicoric Acid inhibits HIV-1 replication in tissue culture[1][2][3]. L-Chicoric Acid ((-)-Chicoric acid) is a dicaffeoyltartaric acid and a potent, selective and reversible HIV-1 integrase inhibitor with an IC50 of ~100 nM. L-Chicoric Acid inhibits HIV-1 replication in tissue culture[1][2][3].

2-METHYLPYRROLIDINE

(R)-2-Methyl-pyrrolidine

C5H11N (85.0891)

A member of the class of pyrrolidines that is pyrrolidine which is substituted by a methyl group at position 2. MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; RGHPCLZJAFCTIK-UHFFFAOYSA-N_STSL_0186_2-Methylpyrrolidine_0500fmol_180831_S2_L02M02_68; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. MS2 deconvoluted using CorrDec from all ion fragmentation data, MetaboLights identifier MTBLS1040; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I.

Michlers ketone

Bis[4-(dimethylamino)phenyl]methanone

C17H20N2O (268.1576)

INTERNAL_ID 250; CONFIDENCE standard compound; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9520; ORIGINAL_PRECURSOR_SCAN_NO 9519 CONFIDENCE standard compound; INTERNAL_ID 250; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9492; ORIGINAL_PRECURSOR_SCAN_NO 9487 CONFIDENCE standard compound; INTERNAL_ID 250; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9500; ORIGINAL_PRECURSOR_SCAN_NO 9498 CONFIDENCE standard compound; INTERNAL_ID 250; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9534; ORIGINAL_PRECURSOR_SCAN_NO 9532 CONFIDENCE standard compound; INTERNAL_ID 250; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9547; ORIGINAL_PRECURSOR_SCAN_NO 9546 CONFIDENCE standard compound; INTERNAL_ID 250; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9470; ORIGINAL_PRECURSOR_SCAN_NO 9468 CONFIDENCE standard compound; INTERNAL_ID 250; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9520; ORIGINAL_PRECURSOR_SCAN_NO 9519 CONFIDENCE standard compound; INTERNAL_ID 2291 CONFIDENCE standard compound; INTERNAL_ID 8123 CONFIDENCE standard compound; INTERNAL_ID 4144

2-Aminobenzenesulfonic acid

1-Aminobenzene-2-sulphonic acid

C6H7NO3S (173.0147)

2-Aminobenzenesulfonic acid is an endogenous metabolite.

Acetylenedicarboxylic acid

2-Butynedioic acid, potassium salt

C4H2O4 (113.9953)

KEIO_ID A128

18R-hydroxy-5Z,8Z,11Z,14Z,16E-eicosapentaenoic acid

(5Z,8Z,11Z,14Z,16E,18R)-18-hydroxyicosa-5,8,11,14,16-pentaenoic acid

C20H30O3 (318.2195)

18R-hydroxy-5Z,8Z,11Z,14Z,16E-eicosapentaenoic acid is also known as 18-HEPE or 18(R)-Hydroxyeicosa-5Z,8Z,11E,14Z,16E-pentaenoate. 18R-hydroxy-5Z,8Z,11Z,14Z,16E-eicosapentaenoic acid is considered to be practically insoluble (in water) and acidic. 18R-hydroxy-5Z,8Z,11Z,14Z,16E-eicosapentaenoic acid is an eicosanoid lipid molecule

Flurenol

C14H10O3 (226.063)

CONFIDENCE standard compound; EAWAG_UCHEM_ID 3094

Eleutherin

Isoeleutherin

C16H16O4 (272.1049)

D000970 - Antineoplastic Agents > D059003 - Topoisomerase Inhibitors > D059005 - Topoisomerase II Inhibitors D004791 - Enzyme Inhibitors [Raw Data] CBA06_Eleutherin_pos_20eV_000003.txt [Raw Data] CBA06_Eleutherin_pos_40eV_000003.txt [Raw Data] CBA06_Eleutherin_pos_50eV_000003.txt [Raw Data] CBA06_Eleutherin_pos_10eV_000003.txt [Raw Data] CBA06_Eleutherin_pos_30eV_000003.txt

4-O-alpha-D-Galactopyranuronosyl-D-galacturonic acid

6-[(2-carboxy-4,5,6-trihydroxyoxan-3-yl)oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

C12H18O13 (370.0747)

Prepd. from pectin by enzymic hydrolysis using yeast or mould pectinases or by acid hydrolysis. Sole or major repeating unit of the pectin class of polysaccharides. Prepd. from pectin by enzymic hydrolysis using yeast or mould pectinases or by acid hydrolysis. Sole or major repeating unit of the pectin class of polysaccharides KEIO_ID D100

4-Hydroxyphenyl-2-propionic acid

4-Hydroxy-α-methylbenzeneacetic acid

C9H10O3 (166.063)

4-Hydroxyphenyl-2-propionic acid belongs to the class of organic compounds known as phenylpropanoic acids. Phenylpropanoic acids are compounds with a structure containing a benzene ring conjugated to a propanoic acid. 4-Hydroxyphenyl-2-propionic acid has been detected in multiple biofluids, such as urine and blood (PMID: 20428313). Within the cell, 4-hydroxyphenyl-2-propionic acid is primarily located in the cytoplasm. A polyphenol metabolite detected in biological fluids [PhenolExplorer] KEIO_ID H099

Leu-Leu-Tyr

(2S)-2-{[(2S)-2-{[(2S)-2-amino-1-hydroxy-4-methylpentylidene]amino}-1-hydroxy-4-methylpentylidene]amino}-3-(4-hydroxyphenyl)propanoic acid

C21H33N3O5 (407.242)

Acquisition and generation of the data is financially supported in part by CREST/JST. KEIO_ID L007

Glucoalyssin

5-Methylsulfinylpentyl glucosinolate

C13H25NO10S3 (451.0641)

A thia-glucosinolic acid that is glucoberteroin in which the sulfur atom of the methyl thioether group has been oxidised to the corresponding sulfoxide. Acquisition and generation of the data is financially supported by the Max-Planck-Society

Cyclic cmp

CYTIDINE 3:5-CYCLIC MONOPHOSPHATE

C9H12N3O7P (305.0413)

Acquisition and generation of the data is financially supported in part by CREST/JST.

Glucobrassicanapin

{[(E)-(1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}hex-5-en-1-ylidene)amino]oxy}sulfonic acid

C12H21NO9S2 (387.0658)

Isolated from rape (Brassica napus) and other Brassica species Glucobrassicanapin is found in many foods, some of which are swede, chinese mustard, chinese cabbage, and horseradish. Glucobrassicanapin is found in brassicas. Glucobrassicanapin is isolated from rape (Brassica napus) and other Brassica sp.

Xenognosin B

7-Hydroxy-3-(2-hydroxy-4-methoxyphenyl)-4H-chromen-4-one

C16H12O5 (284.0685)

Isolated from Trifolium repens (white clover). 2-Hydroxyformononetin is found in many foods, some of which are daikon radish, chervil, pummelo, and turmeric. Xenognosin B is found in green vegetables. Xenognosin B is isolated from Trifolium repens (white clover

Rabelomycin

3,6,8-Trihydroxy-3-methyl-2,4-dihydrobenzo[a]anthracene-1,7,12-trione

C19H14O6 (338.079)

Vulgarin

9-hydroxy-3,5a,9-trimethyl-2H,3H,3aH,4H,5H,5aH,6H,9H,9aH,9bH-naphtho[1,2-b]furan-2,6-dione

C15H20O4 (264.1362)

Vulgarin is found in mugwort. Vulgarin is a constituent of Artemisia vulgaris (mugwort) Constituent of Artemisia vulgaris (mugwort). Vulgarin is found in mugwort.

(-)-cis-Rotenolone

(1R,6R,13R)-13-hydroxy-16,17-dimethoxy-6-(prop-1-en-2-yl)-2,7,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-3,8,10,14(19),15,17-hexaen-12-one

C23H22O7 (410.1365)

(-)-cis-Rotenolone is found in jicama. (-)-cis-Rotenolone is isolated from Pachyrrhizus erosus (yam bean). Isolated from Pachyrrhizus erosus (yam bean). (-)-cis-Rotenolone is found in jicama and pulses.

Archangelicin

2-(9-{[(2Z)-2-methylbut-2-enoyl]oxy}-2-oxo-2H,8H,9H-furo[2,3-H]chromen-8-yl)propan-2-yl (2Z)-2-methylbut-2-enoic acid

C24H26O7 (426.1678)

Constituent of the roots of Angelica archangelica (anglica). Archangelicin is found in many foods, some of which are fats and oils, green vegetables, herbs and spices, and angelica. Archangelicin is found in angelica. Archangelicin is a constituent of the roots of Angelica archangelica (anglica)

chaulmoogric acid

2-Cyclopentene-1-tridecanoicacid, (1S)-

C18H32O2 (280.2402)

A monounsaturated long-chain fatty acid composed of tridecanoic acid having a 2-cyclopentenyl substituent at the 13-position.

Cytidine 2',3'-cyclic phosphate

4-amino-1-[2-hydroxy-6-(hydroxymethyl)-2-oxidotetrahydrofuro[3,4-d][1,3,2]dioxaphosphol-4-yl]pyrimidin-2(1H)-one

C9H12N3O7P (305.0413)

3-Methyl-2-butenal

β,β-Dimethylacrylic aldehyde

C5H8O (84.0575)

3-Methyl-2-butenal, also known as senecialdehyde or 3,3-dimethylacrolein, belongs to the class of organic compounds known as enals. These are alpha,beta-unsaturated aldehydes of the general formula RC=C-CH=O in which the aldehydic C=O function is conjugated to a C=C triple bond at the alpha,beta position. 3-methyl-2-butenal has been detected, but not quantified, in several different foods, such as common oregano, beechnuts, oval-leaf huckleberries, tea leaf willows, and red rice. This could make 3-methyl-2-butenal a potential biomarker for the consumption of these foods. 3-Methyl-2-butenal is a derivative of acrolein that is an alpha, beta-unsaturated carbonyl metabolite. It can be formed endogenously during lipid peroxidation or after oxidative stress, and is considered to play an important role in human carcinogenesis. The endogenously formed acroleins are a constant source of DNA damage, can lead to mutation, and can also induce tumours in humans (PMID:8319634). 3-Methyl-2-butenal, which is an unsaturated aldehyde bearing substitution at the alkene terminus, is a poor inactivator of the enzymes protein tyrosine phosphatases (PTPs). The inactivation of PTPs can yield profound biological consequences arising from the disruption of cellular signalling pathways (PMID:17655273). Present in blackberry, grape brandy, cocoa, currants, baked potato, tea, costmary and white bread. Flavouring ingredient

1,2-Anthracenediol

C14H10O2 (210.0681)

Dihydroxyindole

2,3-Dihydroxyindole

C8H7NO2 (149.0477)

2-Hydroxymuconate

(2E,4Z)-2-hydroxymuconic acid

C6H6O5 (158.0215)

2-INDANONE

C9H8O (132.0575)

3-Hydroxy-1-indanone

C9H8O2 (148.0524)

alpha-Selinene

4a,8-dimethyl-2-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,8a-octahydronaphthalene

C15H24 (204.1878)

Occurs in celery oil and hop (Humulus lupulus) oil. alpha-Selinene is found in many foods, some of which are ginger, lovage, sweet bay, and allspice. alpha-Selinene is found in alcoholic beverages. alpha-Selinene occurs in celery oil and hop (Humulus lupulus) oi

5,6,7,8,3,4,5-Heptamethoxyflavone

2-(3,4,5-Trimethoxyphenyl)-5,6,7,8-tetramethoxy-4H-1-benzopyran-4-one

C22H24O9 (432.142)

Polypodine B

(2beta,3beta,5beta,22R)-2,3,5,14,20,22,25-heptahydroxycholest-7-en-6-one

C27H44O8 (496.3036)

(S)-Ureidoglycolic acid

(S)-[(Aminocarbonyl)amino]hydroxy-acetic acid

C3H6N2O4 (134.0328)

(S)-Ureidoglycolic acid is a substrate of enzyme ureidoglycolate dehydrogenase [EC 1.1.1.154] in purine metabolism pathway (KEGG). [HMDB] (S)-Ureidoglycolic acid is a substrate of enzyme ureidoglycolate dehydrogenase [EC 1.1.1.154] in purine metabolism pathway (KEGG).

Macrocin

2-[6-[5-(4,5-dihydroxy-4,6-dimethyloxan-2-yl)oxy-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-15-[(4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl)oxymethyl]-16-ethyl-4-hydroxy-5,9,13-trimethyl-2,10-dioxo-1-oxacyclohexadeca-11,13-dien-7-yl]acetaldehyde

C45H75NO17 (901.5035)

A macrolide antibiotic that is tylonolide having mono- and diglycosyl moieties attached to two of its hydroxy groups. D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D007933 - Leucomycins

2-Acetolactate

2-hydroxy-2-methyl-3-oxobutanoic acid

C5H8O4 (132.0423)

2-Acetolactate is involved in the butanoate metabolism and pantothenate and CoA biosynthesis pathways. In the butanoate metabolism pathway, 2-Acetolactate is created from 2-(alpha-Hydroxyethyl)thiamine diphosphate by acetolactate synthase [EC:2.2.1.6]. 2-Acetolactate is then converted to (R)-Acetoin by acetolactate decarboxylase [EC:4.1.1.5]. In the pantothenate and CoA pathway, 2-Acetolactate is irreversibly created from pyruvate by acetolactate synthase [EC:2.2.1.6]. 2-Acetolactate is then irreversibly converted to 2,3-Dihydroxy-3-methylbutanoate by ketol-acid reductoisomerase [EC:1.1.1.86]. 2-Acetolactate is involved in the butanoate metabolism and pantothenate and CoA biosynthesis pathways.

2-Ketohexanoic acid

alpha-Ketocaproic acid, sodium salt

C6H10O3 (130.063)

2-Ketohexanoic acid is a potent insulin secretagogue (PMID 7045091). 2-Ketohexanoic acid directly inhibits the ATP-sensitive K+ channel (KATP channel) in pancreatic beta-cells (stimulated in isolated mouse islets), but it is unknown whether direct KATP channel inhibition contributes to insulin release by 2-ketohexanoic acid and related alpha-keto acid anions, which are generally believed to act via beta-cell metabolism (PMID 16014804). 2-Ketohexanoic acid is a potent insulin secretagogue. (PMID 7045091)

Coelenterazine h

Renilla luciferin

C26H21N3O2 (407.1634)

Formylmethanofuran

7-[[(1S)-1-carboxy-4-[[(1S)-1-carboxy-4-[2-[4-[[5-(formamidomethyl)-3-furyl]methoxy]phenyl]ethylamino]-4-oxo-butyl]amino]-4-oxo-butyl]amino]-7-oxo-heptane-1,3,4-tricarboxylic acid

C35H44N4O16 (776.2752)

Allophanic acid

Urea-1-carboxylic acid

C2H4N2O3 (104.0222)

7,8-diaminopelargonate

7,8-Diaminopelargonic acid

C9H20N2O2 (188.1525)

7,8-diaminononanoate, also known as 7,8-dap or 7,8-diaminopelargonic acid, is a member of the class of compounds known as medium-chain fatty acids. Medium-chain fatty acids are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms. Thus, 7,8-diaminononanoate is considered to be a fatty acid lipid molecule. 7,8-diaminononanoate is slightly soluble (in water) and a weakly acidic compound (based on its pKa). 7,8-diaminononanoate can be found in a number of food items such as devilfish, walnut, rapini, and swamp cabbage, which makes 7,8-diaminononanoate a potential biomarker for the consumption of these food products. 7,8-diaminononanoate exists in E.coli (prokaryote) and yeast (eukaryote).

NSC-14980

Cellobiose-1,5-lactone

C12H20O11 (340.1006)

L-2-(Hydroxymethyl)-1,2,3,4-butanetetrol

(+)-(3R)-Hydroxymethylbutane-1,2,3,4-tetrol

C5H12O5 (152.0685)

L-2-(Hydroxymethyl)-1,2,3,4-butanetetrol is found in caraway. L-2-(Hydroxymethyl)-1,2,3,4-butanetetrol is a constituent of the fruit of Foeniculum vulgare (fennel). Constituent of the fruit of Foeniculum vulgare (fennel). L-2-(Hydroxymethyl)-1,2,3,4-butanetetrol is found in caraway and herbs and spices.

Tauropine

2-(2-sulfoethylamino)propanoic acid

C5H11NO5S (197.0358)

A derivative of L-alanine having a 2-sulfoethyl group attached to the alpha-nitrogen.

Rifamycin O

C39H47NO14 (753.2996)

D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D012294 - Rifamycins

Bleomycin B2

Dehydrophleomycin D1

C55H84N20O21S2 (1424.5561)

C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C259 - Antineoplastic Antibiotic C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C2842 - DNA Binding Agent D000970 - Antineoplastic Agents

Raucaffricin

Vomilenine beta-D-glucopyranoside

C27H32N2O8 (512.2159)

Plastoquinol-1

2,3-dimethyl-5-(3-methylbut-2-enyl)-benzene-1,4-diol

C13H18O2 (206.1307)

beta-Alanopine

N-(D-1-Carboxyethyl)-beta-alanine

C6H11NO4 (161.0688)

3-Oxopentanoic acid

3-oxo-pentanoic acid

C5H8O3 (116.0473)

Anthranilyl-CoA

Anthraniloyl-CoA; 2-Aminobenzoyl-CoA

C28H41N8O17P3S (886.1523)

2-Oxosuccinamate

3-(C-hydroxycarbonimidoyl)-2-oxopropanoic acid

C4H5NO4 (131.0219)

This compound belongs to the family of Short-chain Keto Acids and Derivatives. These are keto acids with an alkyl chain the contains less than 6 carbon atoms

Nonane-4,6-dione

C9H16O2 (156.115)

5-Hydroxypentanoic acid

delta-Hydroxypentanoic acid

C5H10O3 (118.063)

5-Hydroxypentanoic acid belongs to the class of organic compounds known as straight chain fatty acids. These are fatty acids with a straight aliphatic chain. 5-Hydroxypentanoic acid has been found to be a microbial metabolite (PMID: 20615997).

Decaprenyl phosphate

[(2Z,6Z,10Z,14Z,18Z,22Z,26Z,30Z,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl] dihydrogen phosphate

C50H83O4P (778.6029)

N-Hydroxy-L-tyrosine

(2S)-2-(hydroxyamino)-3-(4-Hydroxyphenyl)propanoic acid

C9H11NO4 (197.0688)

Biosynthetic intermediate of dhurrin in Sorghum bicolor (sorghum). N-Hydroxy-L-tyrosine is found in many foods, some of which are allspice, asparagus, lemon thyme, and sparkleberry. N-Hydroxy-L-tyrosine is found in cereals and cereal products. Biosynthetic intermediate of dhurrin in Sorghum bicolor (sorghum).

Uridine 2'-phosphate

{[(2R,3R,4R,5R)-2-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)-4-hydroxy-5-(hydroxymethyl)oxolan-3-yl]oxy}phosphonic acid

C9H13N2O9P (324.0359)

Uridine 2- phosphate is a product of the decylclization reaction carried out by the enzyme 2,3-cyclic nucleotide-3-phosphodiesterase (CNPase, EC 3.1.4.37) which hydrolyses Uridine 2,3-cyclic phosphate to Uridine 2-phosphate. CNPase is a unique RNase in that it only cleaves nucleoside 2,3-cyclic phosphates and not the RNA internucleotide linkage, like other RNases such as RNase A and RNase T1. [HMDB] Uridine 2- phosphate is a product of the decylclization reaction carried out by the enzyme 2,3-cyclic nucleotide-3-phosphodiesterase (CNPase, EC 3.1.4.37) which hydrolyses Uridine 2,3-cyclic phosphate to Uridine 2-phosphate. CNPase is a unique RNase in that it only cleaves nucleoside 2,3-cyclic phosphates and not the RNA internucleotide linkage, like other RNases such as RNase A and RNase T1.

3-hydroxyglutamic acid

(2S)-2-amino-3-hydroxypentanedioic acid

C5H9NO5 (163.0481)

An amino dicarboxylic acid that is L-glutamic acid substituted by a hydroxy group at position 3.

phosphonoacetaldehyde

(2-oxoethyl)phosphonic acid

C2H5O4P (123.9925)

10-Formyldihydrofolate

(2S)-2-[(4-{N-[(2-amino-4-oxo-3,4,7,8-tetrahydropteridin-6-yl)methyl]formamido}phenyl)formamido]pentanedioic acid

C20H21N7O7 (471.1502)

10-Formyldihydrofolate is a folate compound that has not been found as a component of intracellular folates in normal tissues but has been identified in the cytosol of methotrexate (MTX)-treated MCF-7 breast cancer cells and normal human myeloid precursor cells. The origin of 10-formyldihydrofolate remains an enigma. Its appearance only in the extracts from MTX-treated cells is not consistent with a simple oxidation of lO-formyl-H4folate during the extraction procedure. This, however, does not exclude the occurrence of spontaneous oxidation of 10-formyl-H4folate within the intact cells prior to the folate extraction. (PMID: 3366769) [HMDB] 10-formyldihydrofolate is a folate compound that has not been found as a component of intracellular folates in normal tissues but has been identified in the cytosol of methotrexate (MTX)-treated MCF-7 breast cancer cells and normal human myeloid precursor cells. The origin of 10-formyldihydrofolate remains an enigma. Its appearance only in the extracts from MTX-treated cells is not consistent with a simple oxidation of lO-formyl-H4folate during the extraction procedure. This, however, does not exclude the occurrence of spontaneous oxidation of 10-formyl-H4folate within the intact cells prior to the folate extraction. (PMID: 3366769).

2-Amino-acetoacetate

2-amino-3-oxobutanoic acid

C4H7NO3 (117.0426)

L-Glutamic acid 5-phosphate

(2S)-2-Amino-5-oxo-5-(phosphonooxy)pentanoic acid

C5H10NO7P (227.0195)

L-Glutamic acid 5-phosphate is an intermediate in the urea cycle and the metabolism of amino groups. It is a substrate of aldehyde dehydrogenase 18 family, member A1 [EC:2.7.2.11 1.2.1.41] (KEGG)In citrulline biosynthesis, it is a substrate of the enzyme glutamate-5-semialdehyde dehydrogenase [EC 1.2.1.41] and in proline synthesis it is a substrate of the enzyme Glutamate 5-kinase [EC 2.7.2.11] (BioCyc). L-Glutamic acid 5-phosphate is an intermediate in the urea cycle and metabolism of amino groups, a substrate of aldehyde dehydrogenase 18 family, member A1 [EC:2.7.2.11 1.2.1.41] (KEGG)

2-Amino-4-oxopentanoate

2-amino-4-oxo-pentanoic acid

C5H9NO3 (131.0582)

Hydroxanthommatin

5,12-Dihydroxanthommatin

C20H15N3O8 (425.0859)

Deoxy-5-methylcytidylate

2-Deoxy-5-methylcytidine-5-monophosphate disodium salt

C10H16N3O7P (321.0726)

9-O-Acetylneuraminic acid

O-Acetylneuraminic acid; O-Acetylated sialic acid

C11H19NO9 (309.106)

The acetate ester of the primary hydroxy group of neuraminic acid.

S-Ribosylhomocysteine

S-(5-Deoxy-D-ribos-5-yl)-L-homocysteine

C9H17NO6S (267.0777)

S-(5-deoxy-beta-D-ribos-5-yl)-L-homocysteine is an S-(5-deoxy-D-ribos-5-yl)-L-homocysteine in which the anomeric centre has beta-configuration. It has a role as an Escherichia coli metabolite. It is functionally related to a L-homocysteine.

20-Hydroxy-leukotriene E4

(5S,6R,7E,9E,11Z,14Z)-6-{[(2R)-2-amino-2-carboxyethyl]sulfanyl}-5,20-dihydroxyicosa-7,9,11,14-tetraenoic acid

C23H37NO6S (455.2341)

20-Hydroxy-leukotriene E4 is a metabolite that can originate from the lipid oxidation of leukotriene E4 (LTE4). LTE4 is a cysteinyl leukotriene. Cysteinyl leukotrienes (CysLTs) are a family of potent inflammatory mediators that appear to contribute to the pathophysiologic features of allergic rhinitis. Nasal blockage induced by CysLTs is mainly due to dilatation of nasal blood vessels which can be induced by the nitric oxide produced through CysLT1 receptor activation. LTE4 activates contractile and inflammatory processes via specific interactions with putative seven transmembrane-spanning receptors that couple to G proteins and subsequent intracellular signaling pathways. LTE4 is metabolized from leukotriene C4 in a reaction catalyzed by gamma-glutamyl transpeptidase and a particulate dipeptidase from kidney (PMID: 12607939, 12432945, 6311078). Leukotrienes are eicosanoids. The eicosanoids consist of the prostaglandins (PGs), thromboxanes (TXs), leukotrienes (LTs), and lipoxins (LXs). The PGs and TXs are collectively identified as prostanoids. Prostaglandins were originally shown to be synthesized in the prostate gland, thromboxanes from platelets (thrombocytes), and leukotrienes from leukocytes, hence the derivation of their names. All mammalian cells except erythrocytes synthesize eicosanoids. These molecules are extremely potent and are able to cause profound physiological effects at very dilute concentrations. All eicosanoids function locally at the site of synthesis through receptor-mediated G-protein linked signaling pathways.

8Z,11Z,14Z-eicosatrienoyl-CoA

{[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-2-({[hydroxy({hydroxy[(3R)-3-hydroxy-3-{[2-({2-[(8Z,11Z,14Z)-icosa-8,11,14-trienoylsulfanyl]ethyl}carbamoyl)ethyl]carbamoyl}-2,2-dimethylpropoxy]phosphoryl}oxy)phosphoryl]oxy}methyl)oxolan-3-yl]oxy}phosphonic acid

C41H68N7O17P3S (1055.3605)

8Z,11Z,14Z-eicosatrienoyl-CoA participates in the biosynthesis of unsaturated fatty acids. 8Z,11Z,14Z-eicosatrienoyl-CoA is converted from (8Z,11Z,14Z)-Icosatrienoic acid via palmitoyl-CoA hydrolase [EC:3.1.2.2].

Unsaturated fatty acids are of similar form, except that one or more alkenyl functional groups exist along the chain, with each alkene substituting a single-bonded "-CH2-CH2-" part of the chain with a double-bonded "-CH=CH-" portion (that is, a carbon double-bonded to another carbon). The differences in geometry between the various types of unsaturated fatty acids, as well as between saturated and unsaturated fatty acids, play an important role in biological processes, and in the construction of biological structures (such as cell membranes). (Wikipedia)

nonaprenyl-4-hydroxybenzoate

3-Nonaprenyl-4-hydroxybenzoic acid

C52H78O3 (750.5951)

SCHEMBL534447

Isobutyraldoxime O-methyl ether

C5H11NO (101.0841)

5-Carboxy-2-oxohept-3-enedioate

5-oxopent-3-ene-1,2,5-tricarboxylic acid

C8H8O7 (216.027)

UDP-4-dehydro-6-deoxy-D-glucose

{[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-hydroxy-2-oxo-1,2-dihydropyrimidin-1-yl)oxolan-2-yl]methoxy}[({[(2R,3R,4R,6R)-3,4-dihydroxy-6-methyl-5-oxooxan-2-yl]oxy}(hydroxy)phosphoryl)oxy]phosphinic acid

C15H22N2O16P2 (548.0445)

UDP-4-dehydro-6-deoxy-D-glucose, also known as UDP-4-keto-6-deoxy-D-glucose, belongs to the class of organic compounds known as pyrimidine nucleotide sugars. These are pyrimidine nucleotides bound to a saccharide derivative through the terminal phosphate group. UDP-4-dehydro-6-deoxy-D-glucose is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, UDP-4-dehydro-6-deoxy-D-glucose has been detected, but not quantified in, several different foods, such as Oregon yampahs, oriental wheat, Chinese mustards, blackcurrants, and pomegranates. This could make UDP-4-dehydro-6-deoxy-D-glucose a potential biomarker for the consumption of these foods. UDP-4-dehydro-6-deoxy-D-glucose is synthesized from UDP-glucose via the enzyme UDP-glucose 4,6-dehydratase. UDP-4-dehydro-6-deoxy-D-glucose is synthesized from UDP-glucose through the enzyme UDP-glucose 4,6-dehydratase. [HMDB]. UDP-4-dehydro-6-deoxy-D-glucose is found in many foods, some of which are alaska wild rhubarb, soy bean, ginkgo nuts, and common beet.

CMP-KDO

CMP-3-deoxy-beta-D-manno-octulosonate

C17H26N3O15P (543.1101)

SCHEMBL4290912

N(6)-[(indol-3-yl)acetyl]-L-lysine

C16H21N3O3 (303.1583)

D006133 - Growth Substances > D010937 - Plant Growth Regulators > D007210 - Indoleacetic Acids

6-Lactoyltetrahydropterin

2-amino-6-(2-hydroxypropanoyl)-3,4,5,6,7,8-hexahydropteridin-4-one

C9H13N5O3 (239.1018)

6-Lactoyltetrahydropterin is a putative intermediate in the de novo synthesis of tetrahydrobiopterin (BH4) pathway, in a reaction involving the enzyme sepiapterin reductase (E.C. 1.1.1.153) in human liver. In brain, an enzyme distinct from sepiapterin reductase catalyzes the TPNH-dependent reduction of 6-pyruvoyl-tetrahydropterin to 6-lactoyl-tetrahydropterin. (PMID: 4004850). In brain, the expression of other enzymes involved in BH4 biosynthesis includes aldose reductase, carbonyl reductase, GTP-cyclohydrolase I, and 6-pyruvoyltetrahydrobiopterin. Sepiapterin reductase expression is increased in Parkinsons disease brain tissue. (PMID: 17270157). 6-Lactoyltetrahydropterin is a putative intermediate in the de novo synthesis of tetrahydrobiopterin (BH4) pathway, in a reaction involving the enzyme sepiapterin reductase (E.C. 1.1.1.153) in human liver. In brain, an enzyme distinct from sepiapterin reductase catalyzes the TPNH-dependent reduction of 6-pyruvoyl-tetrahydropterin to 6-lactoyl-tetrahydropterin. (PMID: 4004850)

1,8-diazacyclotetradecane-2,9-dione

C12H22N2O2 (226.1681)

BENZOYLARGININE NITROANILIDE

N-Benzoyl-D-arginine-4-nitroanilide

C19H22N6O4 (398.1702)

D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D002863 - Chromogenic Compounds D004396 - Coloring Agents

Ac-Phe-3,5-diiodo-Tyr-OH

N-Acetyl-L-phenylalanyl-3,5-diiodo-L-tyrosine

C20H20I2N2O5 (621.9462)

Uridine diphosphate acetylgalactosamine 4-sulfate

[({[(2R,3S,4R,5R)-3-[({[(2R,3R,4R,5R)-5-amino-1,2,4-trihydroxy-6,7-dioxooctan-3-yl]oxy}sulfonyl)oxy]-5-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)-4-hydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy]phosphonic acid

C17H27N3O20P2S (687.0384)

Uridine diphosphate, abbreviated UDP, is a nucleotide. It is an ester of pyrophosphoric acid with the nucleoside uridine. UDP consists of the pyrophosphate group, the pentose sugar ribose, and the nucleobase uracil. [HMDB] Uridine diphosphate, abbreviated UDP, is a nucleotide. It is an ester of pyrophosphoric acid with the nucleoside uridine. UDP consists of the pyrophosphate group, the pentose sugar ribose, and the nucleobase uracil.

4-Oxalomesaconate

(1E)-4-Oxobut-1-ene-1,2,4-tricarboxylate; 4-Oxalomesaconate; 4-Oxalmesaconic acid

C7H6O7 (202.0114)

3alpha,7alpha-Dihydroxycoprostanic acid

(6R)-6-[(1S,2S,5R,7S,9R,10R,11S,14R,15R)-5,9-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]-2-methylheptanoic acid

C27H46O4 (434.3396)

3α,7α-Dihydroxycoprostanic acid is a bile acid excreted in small amounts in the urine of healthy subjects (PMID: 864325). 3α,7α-Dihydroxycoprostanic acid is the precursor to chenodeoxycholic acid, a bile acid. Bile acids are steroid acids found predominantly in the bile of mammals. The distinction between different bile acids is minute, depending only on the presence or absence of hydroxyl groups on positions 3, 7, and 12. Bile acids are physiological detergents that facilitate excretion, absorption, and transport of fats and sterols in the intestine and liver. Bile acids are also steroidal amphipathic molecules derived from the catabolism of cholesterol. They modulate bile flow and lipid secretion, are essential for the absorption of dietary fats and vitamins, and have been implicated in the regulation of all the key enzymes involved in cholesterol homeostasis. Bile acids recirculate through the liver, bile ducts, small intestine, and portal vein to form an enterohepatic circuit. They exist as anions at physiological pH, and consequently require a carrier for transport across the membranes of the enterohepatic tissues. The unique detergent properties of bile acids are essential for the digestion and intestinal absorption of hydrophobic nutrients. Bile acids have potent toxic properties (e.g. membrane disruption) and there are a plethora of mechanisms to limit their accumulation in blood and tissues. 3a,7a-Dihydroxycoprostanic acid is a bile acid excreted in small amounts in the urine of healthy subjects (PMID 864325)

(4-Amino-2-methylpyrimidin-5-YL)methyl dihydrogen phosphate

[(6-imino-2-methyl-1,6-dihydropyrimidin-5-yl)methoxy]phosphonic acid

C6H10N3O4P (219.0409)

Methylisocitric acid

1-hydroxy-1-methylpropane-1,2,3-tricarboxylic acid

C7H10O7 (206.0427)

Methylisocitric acid is a product of bacterial metabolism in the gut. It can be produced by 2-methylisocitrate lyase and by 2-methylisocitrate dehydratase. Methylisocitric acid has also been found to be a metabolite of Candida (https://www.tandfonline.com/doi/pdf/10.1080/00021369.1974.10861293). Methylisocitric acid is a product of bacterial metabolism in the gut. It can be produced by 2-methylisocitrate lyase and by 2-methylisocitrate dehydratase. [HMDB]

2,6-Diamino-4-hydroxy-5-N-methylformamidopyrimidine

N-(2,4-diamino-1,6-dihydro-6-oxo-5-Pyrimidinyl)-N-methyl-formamide

C6H9N5O2 (183.0756)

2,6-Diamino-4-hydroxy-5-N-methylformamidopyrimidine is a methylated derivative of 2,6-Diamino-4-hydroxy-5-N-formamidopyrimidine or FapyGua. It is produced by DNA-formamidopyrimidine glycosylase (EC 3.2.2.23). This enzyme catalyzes the hydrolysis of DNA containing ring-opened 7-methylguanine residues, releasing 2,6-diamino-4-hydroxy-5-(N-methyl)formamidopyrimidine. More specifically, this enzyme catalyzes the removal of oxidized purine bases by cleaving the N-C1 glycosidic bond between the oxidized purine and the deoxyribose sugar. The reaction involves the formation of a covalent enzyme substrate intermediate. Release of the enzyme and free base by a beta-elimination or a beta, gamma-elimination mechanism results in the cleavage of the DNA backbone 3 of the apurinic (AP) site. The presence of this compound in urine is indicative of oxidative damage to DNA (oxidized purine base lesions) [HMDB] 2,6-Diamino-4-hydroxy-5-N-methylformamidopyrimidine is a methylated derivative of 2,6-Diamino-4-hydroxy-5-N-formamidopyrimidine or FapyGua. It is produced by DNA-formamidopyrimidine glycosylase (EC 3.2.2.23). This enzyme catalyzes the hydrolysis of DNA containing ring-opened 7-methylguanine residues, releasing 2,6-diamino-4-hydroxy-5-(N-methyl)formamidopyrimidine. More specifically, this enzyme catalyzes the removal of oxidized purine bases by cleaving the N-C1 glycosidic bond between the oxidized purine and the deoxyribose sugar. The reaction involves the formation of a covalent enzyme substrate intermediate. Release of the enzyme and free base by a beta-elimination or a beta, gamma-elimination mechanism results in the cleavage of the DNA backbone 3 of the apurinic (AP) site. The presence of this compound in urine is indicative of oxidative damage to DNA (oxidized purine base lesions).

8(S)-HPETE

(5Z,9E,11Z,14Z)-(8R)-8-Hydroxyperoxyeicosa-5,9,11,14-tetraenoate

C20H32O4 (336.23)

D-Ribulose

D-(−)-Ribulose

C5H10O5 (150.0528)

19-Oxotestosterone

(1S,2S,10S,11S,14S,15S)-14-hydroxy-15-methyl-5-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-6-ene-2-carbaldehyde

C19H26O3 (302.1882)

19-oxotestosterone, also known as 19-aldehyde-testosterone, belongs to androgens and derivatives class of compounds. Those are 3-hydroxylated C19 steroid hormones. They are known to favor the development of masculine characteristics. They also show profound effects on scalp and body hair in humans. 19-oxotestosterone is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 19-oxotestosterone can be found in a number of food items such as tree fern, italian sweet red pepper, anise, and atlantic herring, which makes 19-oxotestosterone a potential biomarker for the consumption of these food products. 19-oxotestosterone can be found primarily throughout most human tissues. In humans, 19-oxotestosterone is involved in the androgen and estrogen metabolism. 19-oxotestosterone is also involved in a couple of metabolic disorders, which include 17-beta hydroxysteroid dehydrogenase III deficiency and aromatase deficiency. 19-Oxotestosterone is catalyzed by Aromatase (EC 1.14.14.1),also called estrogen synthetase (a cytochrome P450 enzyme which catalyzes the formation of aromatic C18 estrogens from C19 androgens; it is symbolized CYP19) into oestrogens via sequential oxidations at the 19-methyl group. Biosynthesis of estrogens from C19 steroids is catalyzed by aromatase and its tissue-specific expression is determined at least in part by alternative use of tissue-specific promoters, which give rise to transcripts with unique 5-prime noncoding termini.(OMIM 107910).

Psicofuranine

9-D-Psicofuranosyl-6-aminopurine

C11H15N5O5 (297.1073)

Ergosta-5,7,22,24(28)-tetraen-3beta-ol

(3S,10R,13R)-10,13-dimethyl-17-[(E,2R)-6-methyl-5-methylidenehept-3-en-2-yl]-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol

C28H42O (394.3235)

A 3beta-sterol having double bonds in the 5-, 7- and 22-positions and a methylene group at position 24.

AC1NOTCJ

Thiourocanic acid

C6H6N2O2S (170.015)

Isoglutamate

3-Aminopentanedioic acid

C5H9NO4 (147.0532)

Coproporphyrinogen I

3-[9,14,19-tris(2-carboxyethyl)-5,10,15,20-tetramethyl-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1(20),3,5,8,10,13,15,18-octaen-4-yl]propanoic acid

C36H44N4O8 (660.3159)

Coproporphyrinogen I is a porphyrin metabolite arising from heme synthesis. Porphyrins are pigments found in both animal and plant life. Coproporphyrinogen I is a tetrapyrrole dead-end product resulting from the spontaneous oxidation of the methylene bridges of coproporphyrinogen arising from heme synthesis. It is secreted in feces and urine. Coproporphyrinogen I is biosynthesized from the tetrapyrrole hydroxymethylbilane, which is converted by the action of uroporphyrinogen synthase to uroporphyrinogen I. Uroporphyrinogen I is subsequently converted into coproporphyrinogen I through a series of four decarboxylations. Increased levels of coproporphyrinogens can indicate congenital erythropoietic porphyria or sideroblastic anemia, which are inherited disorders. Porphyria is a pathological state characterized by abnormalities of porphyrin metabolism and results in the excretion of large quantities of porphyrins in the urine and in extreme sensitivity to light. A large number of factors are capable of increasing porphyrin excretion, owing to different and multiple causes and etiologies: (1) the main site of the chronic hepatic porphyria disease process concentrates on the liver, (2) a functional and morphologic liver injury is almost regularly associated with this chronic porphyria, and (3) the toxic form due to occupational and environmental exposure takes mainly a subclinical course. Hepatic factors include disturbance in coproporphyrinogen metabolism, which results from inhibition of coproporphyrinogen oxidase as well as from the rapid loss and diminished utilization of coproporphyrinogen in the hepatocytes. This may also explain why coproporphyrin, its autoxidation product, predominates physiologically in the urine. Decreased biliary excretion of coproporphyrin leading to a compensatory urinary excretion. Therefore, the coproporphyrin ring isomer ratio becomes a sensitive index for impaired liver function, intrahepatic cholestasis, and disturbed activity of hepatic uroporphyrinogen decarboxylase. In itself, secondary coproporphyrinuria is not associated with porphyria symptoms of a hepatologic-gastroenterologic, neurologic, or dermatologic order, even though coproporphyrinuria can occur with such symptoms (PMID: 3327428). Under certain conditions, coproporphyrinogen I can act as a phototoxin, a neurotoxin, and a metabotoxin. A phototoxin leads to cell damage upon exposure to light. A neurotoxin causes damage to nerve cells and nerve tissues. A metabotoxin is an endogenously produced metabolite that causes adverse health effects at chronically high levels. Chronically high levels of porphyrins are associated with porphyrias such as porphyria variegate, acute intermittent porphyria, hereditary coproporphyria (HCP), congenital erythropoietic porphyria, and sideroblastic anemia. There are several types of porphyrias (most are inherited). Hepatic porphyrias are characterized by acute neurological attacks (seizures, psychosis, extreme back and abdominal pain, and an acute polyneuropathy), while the erythropoietic forms present with skin problems (usually a light-sensitive blistering rash and increased hair growth). The neurotoxicity of porphyrins may be due to their selective interactions with tubulin, which disrupt microtubule formation and cause neural malformations (PMID: 3441503). Coproporphyrinogen I can be found in a number of food items, including cascade huckleberry, hyacinth bean, horseradish tree, and watercress. Formed by Uroporphyrinogen decarboxylase from Uroporphyrinogen I by decarboxylation of 4 acetates. [HMDB]. Coproporphyrinogen I is found in many foods, some of which are alpine sweetvetch, japanese persimmon, komatsuna, and celery leaves.

N1-(alpha-D-ribosyl)-5,6-dimethyl-benzimidazole

(2S,5R)-2-(5,6-dimethyl-1H-1,3-benzodiazol-1-yl)-5-(hydroxymethyl)oxolane-3,4-diol

C14H18N2O4 (278.1267)

N1-(alpha-D-ribosyl)-5,6-dimethyl-benzimidazole is an intermediate in riboflavin metabolism. It is converted from N1-(5-Phospho-alpha-D-ribosyl)-5,6-dimethylbenzimidazole via dephosphorylation by the enzyme phosphohistidine phosphatase 1 (EC 3.1.3.-). Humans do not have all the enzymes needed to synthesize or metabolize riboflavin. However, gut microflora do have the necessary enzymatic machinery to produce and metabolize this vitamin. Riboflavin (or vitamin B2) is an easily absorbed micronutrient with a key role in maintaining health in humans and animals. It is the central component of the cofactors FAD and FMN, and is therefore required by all flavoproteins. Riboflavin is yellow or yellow-orange in color and in addition to being used as a food coloring it is also used to fortify some foods including baby foods, breakfast cereals, pastas, sauces, processed cheese, fruit drinks, vitamin-enriched milk products, some energy drinks, and vitamin supplements. [HMDB] N1-(alpha-D-ribosyl)-5,6-dimethyl-benzimidazole is an intermediate in riboflavin metabolism. It is converted from N1-(5-Phospho-alpha-D-ribosyl)-5,6-dimethylbenzimidazole via dephosphorylation by the enzyme phosphohistidine phosphatase 1 (EC 3.1.3.-). Humans do not have all the enzymes needed to synthesize or metabolize riboflavin. However, gut microflora do have the necessary enzymatic machinery to produce and metabolize this vitamin. Riboflavin (or vitamin B2) is an easily absorbed micronutrient with a key role in maintaining health in humans and animals. It is the central component of the cofactors FAD and FMN, and is therefore required by all flavoproteins. Riboflavin is yellow or yellow-orange in color and in addition to being used as a food coloring it is also used to fortify some foods including baby foods, breakfast cereals, pastas, sauces, processed cheese, fruit drinks, vitamin-enriched milk products, some energy drinks, and vitamin supplements.

2-Hexaprenyl-3-methyl-6-methoxy-1,4 benzoquinone

3-[(2E,6E,10E,14E,18E)-3,7,11,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaen-1-yl]-5-methoxy-2-methylcyclohexa-2,5-diene-1,4-dione

C38H56O3 (560.4229)

2-Hexaprenyl-3-methyl-6-methoxy-1,4 benzoquinone is involved in the ubiquinone biosynthesis pathway. 2-Hexaprenyl-3-methyl-6-methoxy-1,4 benzoquinone is created from 2-Hexaprenyl-6-methoxy-1,4-benzoquinone by ubiquinone biosynthesis methyltransferase [EC:2.1.1.-]. 2-Hexaprenyl-3-methyl-6-methoxy-1,4 benzoquinone is then converted to 2-Hexaprenyl-3-methyl-5-hydroxy-6-methoxy-1,4-benzoquinone by ubiquinone biosynthesis monooxygenase Coq7 [EC:1.14.13.-]. [HMDB] 2-Hexaprenyl-3-methyl-6-methoxy-1,4 benzoquinone is involved in the ubiquinone biosynthesis pathway. 2-Hexaprenyl-3-methyl-6-methoxy-1,4 benzoquinone is created from 2-Hexaprenyl-6-methoxy-1,4-benzoquinone by ubiquinone biosynthesis methyltransferase [EC:2.1.1.-]. 2-Hexaprenyl-3-methyl-6-methoxy-1,4 benzoquinone is then converted to 2-Hexaprenyl-3-methyl-5-hydroxy-6-methoxy-1,4-benzoquinone by ubiquinone biosynthesis monooxygenase Coq7 [EC:1.14.13.-].

2-Octaprenyl-3-methyl-6-methoxy-1,4-benzoquinone

5-methoxy-2-methyl-3-(3,7,11,15,19,23,27,31-octamethyldotriaconta-2,6,10,14,18,22,26,30-octaen-1-yl)cyclohexa-2,5-diene-1,4-dione

C48H72O3 (696.5481)

Leucocyanidin

(2R,3S)-2-(3,4-Dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,4,5,7-tetrol

C15H14O7 (306.0739)

Leucocyanidin is an active anti-ulcerogenic ingredient was extracted from Litchi Chinensis. Leucocyanidin demonstrates a significant protective effect against Aspirin-induced erosions in rat models[1]. Leucocyanidin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=480-17-1 (retrieved 2024-09-18) (CAS RN: 480-17-1). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

Dihydrotricetin

5,7,3,4,5-Pentahydroxyflavanone

C15H12O7 (304.0583)

Isopyridoxal

5-Hydroxy-4-(hydroxymethyl)-6-methyl-3-pyridinecarboxaldehyde

C8H9NO3 (167.0582)

Isopyridoxal is an active vitamer of the B6 complex in humans. (PMID 2208740). Vitamin B(6) is an essential component in human diet. (PMID 12686115). Vitamin B6 status (together with other vitamins from the B complex) is also related to Hyperhomocysteinemia, which has been linked to an increased risk for cardiovascular (CV) disease. (PMID 16407736). Isopyridoxal is an active vitamer of the B6 complex in humans. (PMID 2208740)

ent-16-Kaurene

(4R,9R,10R,13R)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane

C20H32 (272.2504)

Phyllocladene is found in fats and oils. Phyllocladene is a constituent of sunflower oil.

3-Butyn-1-al

C4H4O (68.0262)

3-Butyn-1-al is an intermediate in Butanoate metabolism (KEGG ID C06145). It is the third to last step in the synthesis and degradation of ketone bodies and is converted from 3-Butyn-1-ol via the enzyme alcohol dehydrogenase (acceptor) [EC:1.1.99.8]. It is then converted to 3-Butynoate via the enzyme aldehyde dehydrogenase (NAD+) [EC:1.2.1.3]. 3-Butyn-1-al is an intermediate in Butanoate metabolism (KEGG ID

Hygrine

1-[(2R)-1-methylpyrrolidin-2-yl]propan-2-one

C8H15NO (141.1154)

Hygrine, also known as (+)-hygrine or (+)-N-methyl-2-acetonylpyrrolidine, belongs to alkaloids and derivatives class of compounds. Those are naturally occurring chemical compounds that contain mostly basic nitrogen atoms. This group also includes some related compounds with neutral and even weakly acidic propertiesand is also some synthetic compounds of similar structure are attributed to alkaloids. In addition to carbon, hydrogen and nitrogen, alkaloids may also contain oxygen, sulfur and more rarely other elements such as chlorine, bromine, and phosphorus. Hygrine is soluble (in water) and an extremely weak acidic compound (based on its pKa). Hygrine can be found in pomegranate, which makes hygrine a potential biomarker for the consumption of this food product. Hygrine is a pyrrolidine alkaloid, found mainly in coca leaves (0.2\\%). It was first isolated by Carl Liebermann in 1889 (along with a related compound cuscohygrine) as an alkaloid accompanying cocaine in coca. Hygrine is extracted as a thick yellow oil, having a pungent taste and odor .

2-Hydroxy-6-keto-2,4-heptadienoate

2-Hydroxy-6-oxo-2,4-heptadienoic acid

C7H8O4 (156.0423)

1-Deoxy-D-xylulose

(2S,3S,4R)-2-(hydroxymethyl)oxolane-3,4-diol

C5H10O4 (134.0579)

1-Deoxy-D-xylulose is a product of the splitting up of Pyridoxine (an intermediate in Vitamin B6 metabolism) into two components (the other one being 4-Hydroxy-L-threonine). (KEGG) [HMDB] 1-Deoxy-D-xylulose is a product of the splitting up of Pyridoxine (an intermediate in Vitamin B6 metabolism) into two components (the other one being 4-Hydroxy-L-threonine). (KEGG).

FT-0699926

3-[(1R,2S,3S,5Z,7S,8S,9Z,13S,14Z,17R,18R)-3,13,17-tris(2-carboxyethyl)-2,7,18-tris(carboxymethyl)-1,2,5,7,12,12,15,17-octamethyl-3,8,13,18,19,22-hexahydrocorrin-8-yl]propanoic acid

C45H60N4O14 (880.4106)

Precorrin-4

C44H52N4O17 (908.3327)

5-(5-(2,6-Dichloro-4-(4,5-Dihydro-2-Oxazoly)phenoxy)pentyl)-3-Methyl Isoxazole

5-{5-[2,6-dichloro-4-(4,5-dihydro-1,3-oxazol-2-yl)phenoxy]pentyl}-3-methyl-1,2-oxazole

C18H20Cl2N2O3 (382.0851)

trans-3-Chloroacrylic acid

(2E)-3-chloroprop-2-enoic acid

C3H3ClO2 (105.9822)

This compound belongs to the family of Enones. These are compounds containing the enone functional group, with the structure RC(=O)CR

Erythromycin

(3R,4S,5S,6R,7R,9R,11R,12R,13S,14R)-4-[(2R,4R,5S,6S)-4,5-dihydroxy-4,6-dimethyloxan-2-yl]oxy-6-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-7,12,13-trihydroxy-3,5,7,9,11,13-hexamethyl-oxacyclotetradecane-2,10-dione

C36H65NO13 (719.4456)

D004791 - Enzyme Inhibitors > D011500 - Protein Synthesis Inhibitors D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents D005765 - Gastrointestinal Agents

Clavaldehyde

7-oxo-3-(2-oxoethylidene)-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid

C8H7NO5 (197.0324)

An organic heterobicyclic compound that is clavulanic acid in which the allylic alcohol group has been oxidised to the corresponding aldehyde.

14-apo-beta-carotenal

5,9-dimethyl-11-(2,6,6-trimethylcyclohexen-1-yl)undeca-2,4,6,8,10-pentaenal

C22H30O (310.2297)

D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids

3,6-dichlorocatechol

3,6-Dichloro-1,2-benzenediol

C6H4Cl2O2 (177.9588)

3,6-dichlorocatechol, also known as 3,6-dichloro-1,2-benzenediol, is a member of the class of compounds known as 3-chlorocatechols. 3-chlorocatechols are chlorocatechols with the chlorine atom attached at position C3 of the benzene ring. 3,6-dichlorocatechol is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). 3,6-dichlorocatechol can be found in a number of food items such as gooseberry, jicama, nutmeg, and lingonberry, which makes 3,6-dichlorocatechol a potential biomarker for the consumption of these food products.

2,6-Dichlorohydroquinone

2,6-DICHLORO-1,4-HYDROQUINONE

C6H4Cl2O2 (177.9588)

triclofos

2,2,2-Trichloroethyl dihydrogen phosphate, sodium salt

C2H4Cl3O4P (227.8913)

N - Nervous system > N05 - Psycholeptics > N05C - Hypnotics and sedatives C78272 - Agent Affecting Nervous System > C29756 - Sedative and Hypnotic

dimethisterone

Dimethisterone; Dimethisterone anhydrous

C23H32O2 (340.2402)

C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone D012102 - Reproductive Control Agents > D003270 - Contraceptive Agents

Phthalylsulfathiazole

2-[[[4-[(2-Thiazolylamino)sulphonyl]phenyl]amino]carbonyl]benzoic acid

C17H13N3O5S2 (403.0297)

A - Alimentary tract and metabolism > A07 - Antidiarrheals, intestinal antiinflammatory/antiinfective agents > A07A - Intestinal antiinfectives > A07AB - Sulfonamides C254 - Anti-Infective Agent > C29739 - Sulfonamide Anti-Infective Agent D000890 - Anti-Infective Agents > D013432 - Sulfathiazoles D000890 - Anti-Infective Agents > D013424 - Sulfanilamides

Propoxycaine

2-(Diethylamino)ethyl 4-amino-2-propoxybenzoic acid

C16H26N2O3 (294.1943)

D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants > D000777 - Anesthetics D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents C78272 - Agent Affecting Nervous System > C245 - Anesthetic Agent

Palmitone

hentriacontan-16-one

C31H62O (450.48)

Constituent of Piper nigrum (pepper). Palmitone is found in herbs and spices, pepper (spice), and potato. Palmitone is found in herbs and spices. Palmitone is a constituent of Piper nigrum (pepper)

Thial-1-Propene-1-thiol S-oxide

C3H6OS (90.0139)

Lachrymatory factor of onion (Allium cepa). Thial-1-Propene-1-thiol S-oxide is found in garden onion and onion-family vegetables. Thial-1-Propene-1-thiol S-oxide is found in garden onion. Lachrymatory factor of onion (Allium cepa).

Eutypine

Eutypine; 4-Hydroxy-3-(3-methyl-3-butene-1-ynyl)benzaldehyde

C12H10O2 (186.0681)

Eutypine is a member of the class of compounds known as hydroxybenzaldehydes. Hydroxybenzaldehydes are organic aromatic compounds containing a benzene ring carrying an aldehyde group and a hydroxyl group. Eutypine is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Eutypine can be found in common grape, which makes eutypine a potential biomarker for the consumption of this food product.

Albafuran A

4-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-5-(6-hydroxy-1-benzofuran-2-yl)benzene-1,3-diol

C24H26O4 (378.1831)

Albafuran A is found in fruits. Albafuran A is a constituent of white mulberry (Morus alba) Constituent of white mulberry (Morus alba). Albafuran A is found in fruits.

Dihydroeuparin

5-Acetyl-6-hydroxy-2-isopropenyl-2,3-dihydrobenzofuran

C13H14O3 (218.0943)

Glaucarubolone

C20H26O8 (394.1628)

Asclepin

3-O-Acetylcalotropin

C31H42O10 (574.2778)

D020011 - Protective Agents > D002316 - Cardiotonic Agents > D002301 - Cardiac Glycosides

Avenacin A-1

oat triterpenoid saponin

C55H83NO21 (1093.5457)

Senegin II

(2S,3R,4S,6aR,6bR,8aS,12aS,14bR)-8a-[(2S,3R,4S,5R,6R)-3-[(2S,3R,4S,5R,6S)-5-[(2S,3R,4R,5R)-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-5-[(E)-3-(3,4-dimethoxyphenyl)prop-2-enoyl]oxy-4-hydroxy-6-methyloxan-2-yl]oxycarbonyl-2-hydroxy-6b-(hydroxymethyl)-4,6a,11,11,14b-pentamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid

C70H104O32 (1456.651)

A triterpenoid saponin isolated from Polygala senega var latifolia and has been shown to exhibit hypoglycemic activity.

Aurasperone D

5,6-dihydroxy-10-{5-hydroxy-6,8-dimethoxy-2-methyl-4-oxo-4H-benzo[g]chromen-7-yl}-8-methoxy-2-methyl-4H-benzo[g]chromen-4-one

C31H24O10 (556.1369)

Aurasperone D is found in mango. Aurasperone D is a mycotoxin from Aspergillus niger infected mango fruits. Mycotoxin from Aspergillus niger infected mango fruits. Aurasperone D is found in mango.

Affinine

17-Hydroxyvobasan-3-one

C20H24N2O2 (324.1838)

Sorgolactone

3-methyl-5-{[(3Z)-8-methyl-2-oxo-2H,3H,3aH,4H,5H,6H,7H,8H,8bH-indeno[1,2-b]furan-3-ylidene]methoxy}-2,5-dihydrofuran-2-one

C18H20O5 (316.1311)

Sorgolactone is found in cereals and cereal products. Sorgolactone is isolated from the roots of Sorghum bicolor (sorghum) (genuine host plant for Striga species) Strigolactones are plant hormones that have been implicated in inhibition of shoot branching. Strigolactones are carotenoid-derived and trigger germination of parasitic plant seeds (for example striga from which they gained their name) and stimulate symbiotic mycorrhizal fungi. Strigolactones contain a labile ether bond that is easily hydrolysed in the rhizosphere meaning that there is a large concentration gradient between areas near the root and those further away. Isolated from the roots of Sorghum bicolor (sorghum) (genuine host plant for Striga subspecies)

Leptodactylone

8-hydroxy-5,7-dimethoxy-chromen-2-one

C11H10O5 (222.0528)

Arbusculin A

[3aS-(3aalpha,5abeta,9alpha,9aalpha,9bbeta)]-Decahydro-9-hydroxy-5a,9-dimethyl-3-methylenenaphtho[1,2-b]furan-2(3H)-one

C15H22O3 (250.1569)

A sesquiterpene lactone isolated from Saussureae Radix and has been shown to exhibit inhibitory activity against melanogenesis.

DivK1c_000746

alpha-Cyclocostunolide

C15H20O2 (232.1463)

eremantholide

Eremantholide A

C19H24O6 (348.1573)

Melampodin A

methyl (2E,4S,6R,7E,9S,10S,11S)-10-[(2R,3R)-2,3-dimethyloxirane-2-carbonyl]oxy-9-hydroxy-3-methyl-12-methylidene-13-oxo-5,14-dioxatricyclo[9.3.0.04,6]tetradeca-2,7-diene-8-carboxylate

C21H24O9 (420.142)

Salonitenolide

C15H20O4 (264.1362)

Psychotrin

Ipecac (Psychotrine)

C28H36N2O4 (464.2675)

Strobopinin

(2S) -2,3-Dihydro-5,7-dihydroxy-6-methyl-2-phenyl-4H-1-benzopyran-4-one

C16H14O4 (270.0892)

A dihydroxyflavanone that is (2S)-flavanone substituted by hydroxy groups at positions 5 and 7 and a methyl group at position 6 respectively.

N-Acetylpuromycin

C24H31N7O6 (513.2336)

trichlorohydroquinone

2,3,5-Trichlorobenzene-1,4-diol

C6H3Cl3O2 (211.9199)

Caranine

NSC406043

C16H17NO3 (271.1208)

An indolizidine alkaloid that is galanthan substituted by analpha-hydroxy group at position 1 and a methylenedioxy group across position 9 and 10. An alkaloid commonly found in the members of the family amaryllidaceae.

Isogentisin

9H-Xanthen-9-one, 1,3-dihydroxy-7-methoxy- (9ci)

C14H10O5 (258.0528)

Isogentisin is found in alcoholic beverages. Isogentisin is isolated from roots of Gentiana lutea (yellow gentian

Echinone

Echinone; 6-((1S)-1-(Acetyloxy)-4-methyl-3-pentenyl)-8-hydroxy-5-methoxy-1,4-naphthalenedione

C19H20O6 (344.126)

Isodiospyrin

[1,2-Binaphthalene]-5,5,8,8-tetrone, 1,4-dihydroxy-2,3-dimethyl-, (R)- (8CI); (1R)-1,4-Dihydroxy-2,3-dimethyl[1,2-binaphthalene]-5,5,8,8-tetrone; (-)-Isodiospyrin

C22H14O6 (374.079)

Isodiospyrin is a member of biphenyls. Isodiospyrin is a natural product found in Diospyros morrisiana, Diospyros verrucosa, and other organisms with data available. Isodiospyrin, a natural dimeric naphthoquinone, is a human DNA topoisomerase I (Topoisomerase) inhibitor. Isodiospyrin can prevent both DNA relaxation and kinase activities of human topoisomerase I. Isodiospyrin shows anticancer, antibacterial and antifungal activities[1][2][3]. Isodiospyrin, a natural dimeric naphthoquinone, is a human DNA topoisomerase I (Topoisomerase) inhibitor. Isodiospyrin can prevent both DNA relaxation and kinase activities of human topoisomerase I. Isodiospyrin shows anticancer, antibacterial and antifungal activities[1][2][3].

Prenylbenzoquinone

2-Prenyl-1,4-benzoquinone

C11H12O2 (176.0837)

crenatoside

Orobanchoside; Crenatoside

C29H34O15 (622.1898)

Flindersiamine

8-Methoxy-6,7-methylenedioxydictamnine

C14H11NO5 (273.0637)

Furofoline

5-Hydroxy-11-methylfuro[2,3-c]acridin-6(11H)-one, 9ci

C16H11NO3 (265.0739)

Furofoline is found in herbs and spices. Furofoline is an alkaloid from the roots of Ruta graveolens (rue Alkaloid from the roots of Ruta graveolens (rue). Furofoline is found in herbs and spices.

Multifidol

2-Methyl-1-(2,4,6-trihydroxyphenyl)butan-1-one

C11H14O4 (210.0892)

A butanone that is the 2-methylbutanoyl derivative of phloroglucinol.

Maculine

1,3-Dioxolo(4,5-g)furo(2,3-b)quinoline, 9-methoxy-

C13H9NO4 (243.0532)

Grevillol

5-tridecylbenzene-1,3-diol

C19H32O2 (292.2402)

Apoatropine

BENZENEACETIC ACID, .ALPHA.-METHYLENE-, (3-ENDO)-8-METHYL-8-AZABICYCLO(3.2.1)OCT-3-YL ESTER

C17H21NO2 (271.1572)

Calystegin A3

8-azabicyclo[3.2.1]octane-1,2,3-triol

C7H13NO3 (159.0895)

Alkaloid from Solanum tuberosum (potato). Calystegin A3 is found in many foods, some of which are eggplant, alcoholic beverages, potato, and sweet potato. Calystegin A3 is found in alcoholic beverages. Calystegin A3 is an alkaloid from Solanum tuberosum (potato).

Calystegine B2

8-azabicyclo[3.2.1]octane-1,2,3,4-tetrol

C7H13NO4 (175.0845)

Alkaloid from Solanum tuberosum (potato), Solanum melongena (aubergine). Calystegine B2 is found in many foods, some of which are alcoholic beverages, fruits, swamp cabbage, and eggplant. Calystegine B2 is found in alcoholic beverages. Calystegine B2 is an alkaloid from Solanum tuberosum (potato), Solanum melongena (aubergine).

Simplexoside

(+)-Piperitol beta-glucoside

C26H30O11 (518.1788)

Chlorpromazine-N-oxide

3-(2-chloro-10H-phenothiazin-10-yl)-N,N-dimethylpropanamine oxide

C17H19ClN2OS (334.0907)

Chlorpromazine-N-oxide is a metabolite of chlorpromazine. Chlorpromazine (as chlorpromazine hydrochloride, abbreviated CPZ; marketed in the United States as Thorazine and elsewhere as Largactil) is a typical antipsychotic. First synthesized on December 11, 1950, chlorpromazine was the first drug developed with specific antipsychotic action, and would serve as the prototype for the phenothiazine class of drugs, which later grew to comprise several other agents. (Wikipedia)

1,3,6,8-TCDD

1,3,6,8-TETRACHLORODIBENZO-P-DIOXIN

C12H4Cl4O2 (319.8965)

D009676 - Noxae > D013723 - Teratogens > D000072317 - Polychlorinated Dibenzodioxins

Diclobutrazol

1 (2,4-Dichlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pentan-3-ol

C15H19Cl2N3O (327.0905)

Bacteriochlorophyll b

(7R,8Z)-bacteriochlorophyll b

C55H72MgN4O6 (908.5302)

S-Octyl GSH

S-Octyl glutathione

C18H33N3O6S (419.209)

S-(PGA1)-glutathione

7-[(2R)-3-{[(2R)-2-{[(4S)-4-amino-4-carboxy-1-hydroxybutylidene]amino}-2-[(carboxymethyl)-C-hydroxycarbonimidoyl]ethyl]sulphanyl}-2-[(1E)-3-hydroxyoct-1-en-1-yl]-5-oxocyclopentyl]heptanoic acid

C30H49N3O10S (643.3138)

S-(PGA1)-glutathione is the gluthathione conjugate of prostaglanding A1. This conjugate is a substrate for MRP2 (31). PGA1 was observed to be able to inhibit. MRP2-mediated transport of DNP-SG quite well. S-(PGA1)-glutathione is the gluthathione conjugate of prostaglanding A1. This conjugate is a substrate for MRP2 (31). PGA1 was observed to be able to inhibit

S-(p-Azidophenacyl)glutathione

S-(4-Azidophenacyl)glutathione; S-(p-Azidophenacyl)glutathione

C18H22N6O7S (466.1271)

Chromotropic acid

4,5-Dihydroxy-2,7-naphthalenedisulfonic acid

C10H8O8S2 (319.9661)

NAc-AAA-ME

Methyl-N-acetyl-N-L-alanyl-N-L-alanyl alaninate

C12H21N3O5 (287.1481)

N-Ethylmaleimide-S-glutathione

C16H22N4O8S (430.1158)

delta8,14-Sterol

(2S,5S,6S,7S,14R,15R)-2,6,15-trimethyl-14-[(2R)-6-methyl-5-methylideneheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(10),11-dien-5-ol

C29H46O (410.3548)

delta8,14-Sterol, also known as 4alpha-methyl-5alpha-ergosta-8,14,24(28)-trien-3beta-ol, belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton. Thus, delta8,14-sterol is considered to be a sterol lipid molecule. delta8,14-Sterol is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. delta8,14-Sterol is an intermediate in the biosynthesis of steroids and is converted from O-butusifoliol via the enzyme cytochrome P450, family 51, subfamily A (sterol 14-demethylase) (EC 1.14.13.70). It is then converted into 4-alpha-methylfecosterol via the enzyme delta14-sterol reductase (EC 1.3.1.70). Constituent of wheat germ oil (Triticum aestivum)

(3beta,4beta,5alpha)-4-Methylergosta-7,24(28)-dien-3-ol

(1R,2S,5S,6S,7S,11R,14R,15R)-2,6,15-trimethyl-14-[(2R,5Z)-5-(propan-2-yl)hept-5-en-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-5-ol

C30H50O (426.3861)

(3beta,4beta,5alpha)-4-Methylergosta-7,24(28)-dien-3-ol is isolated from marigold (Calendula officinalis) flowers.

Mikamycin B

N-(3-{[4-(dimethylamino)phenyl]methyl}-12-ethyl-4,16-dimethyl-2,5,11,14,18,21,24-heptaoxo-19-phenyl-17-oxa-1,4,10,13,20-pentaazatricyclo[20.4.0.0⁶,¹⁰]hexacosan-15-yl)-3-hydroxypyridine-2-carboxamide

C45H54N8O10 (866.3963)

D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D025361 - Streptogramins Pristinamycin IA (Mikamycin B) is a cycle-peptidic macrolactone antibiotic. Pristinamycin IA is a substrate of P-glycoprotein and inhibits its function. Pristinamycin IA is active against StaphyloEoccus and Srreptococcus[1].

omega-COOH-LTE4NAc

omega-Carboxy-N-acetyl-LTE4; (7E,9E,11Z,14Z)-(5S,6R)-6-((N-Acetyl)cystein-S-yl)-5-hydroxyeicosa-7,9,11,14-tetraen-1,20-dioate; omega-COOH-LTE4NAc

C25H37NO8S (511.224)

16-epivellosimine

(1S,12S,13S,14R,15E)-15-ethylidene-3,17-diazapentacyclo[12.3.1.0^{2,10}.0^{4,9}.0^{12,17}]octadeca-2(10),4(9),5,7-tetraene-13-carbaldehyde

C19H20N2O (292.1576)

16-epivellosimine is a member of the class of compounds known as macroline alkaloids. Macroline alkaloids are alkaloids with a structure that is based on the tetracyclic macroline skeleton. The macroline skeleton arises by scission of the C-21 to N-4 bond of the akuammilan skeleton, and mostly occurs in bisindole alkaloids. 16-epivellosimine is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 16-epivellosimine can be found in a number of food items such as bitter gourd, red raspberry, orange bell pepper, and star anise, which makes 16-epivellosimine a potential biomarker for the consumption of these food products.

Anhydrovinblastin

Vincaleukoblastine, 3,4-didehydro-4-deoxy-

C46H56N4O8 (792.4098)

4,21-Dehydrocorynantheine aldehyde

C21H23N2O3+ (351.1709)

SK&F 91581

N-[3-(1H-imidazol-4-yl)propyl]-N-methylthiourea

C8H14N4S (198.0939)

magnesium;methyl (3R,21S,22S)-11,16-bis(ethenyl)-12,17,21,26-tetramethyl-4-oxo-22-[3-oxo-3-[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-23,25-diaza-7,24-diazanidahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1,5,8(26),9,11,13(25),14,16,18,20(23)-decaene-3-carboxylate

magnesium;methyl (3R,21S,22S)-11,16-bis(ethenyl)-12,17,21,26-tetramethyl-4-oxo-22-[3-oxo-3-[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-23,25-diaza-7,24-diazanidahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1,5,8(26),9,11,13(25),14,16,18,20(23)-decaene-3-carboxylate

C55H70MgN4O5 (890.5196)

Sventenic acid

ent-7α-Hydroxykaur-16-en-19-oic acid

C20H30O3 (318.2195)

Neoabietadiene

Abieta-8(14),13(15)-diene

C20H32 (272.2504)

palustradiene

C20H32 (272.2504)

Methanophenazine

Methanophenazine; 2-(2,3-Dihydro-all-trans-pentaprenyloxy)phenazine; 2-(2,3-Dihydropentaprenyloxy)phenazine

C37H50N2O (538.3923)

8,8a-Deoxyoleandolide

(3R,4S,5R,6S,7S,9R,11R,12S,13R,14R)-4,6,12-trihydroxy-3,5,7,9,11,13,14-heptamethyl-oxacyclotetradecane-2,10-dione

C20H36O6 (372.2512)

8,8a-Deoxyoleandolide is a naturally occurring sesquiterpene lactone, which is a type of organic compound derived from the metabolism of plants. It is characterized by the absence of an oxygen atom at the 8 and 8a positions in its molecular structure, which differentiates it from the related compound oleandolide. Sesquiterpene lactones are known for their biological activities, such as cytotoxic, anti-inflammatory, and antimicrobial properties. 8,8a-Deoxyoleandolide may be found in various plant species and could be of interest for pharmaceutical research due to its potential therapeutic effects. The compound's structure typically includes a lactone ring fused with a sesquiterpene framework, and it may exhibit various substituents depending on its source and the specific plant it is derived from. 13-Deethyl-6,12-dideoxy-13-methylerythronolide A. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=53428-54-9 (retrieved 2024-07-15) (CAS RN: 53428-54-9). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

10-Deoxymethynolide

C17H28O4 (296.1987)

A macrolide that consists of oxacyclododec-9-ene-2,8-dione bearing four methyl substituents at positions 3, 5, 7 and 11 as well as a hydroxy group at position 4 and an ethyl substituent at position 12. The aglycone of the macrolide antibiotic 10-deoxymethymycin.

Narbonolide

C20H32O5 (352.225)

A 14-membererd macrolide containing seven stereocentres carrying one ethyl, one hydroxy and five methyl substituents. It is the aglycone of the antibiotic narbonomycin and an intermediate in the biosynthesis of pikromycin.

2-Butenyl-4-methylthreonine

(E)-2-Butenyl-4-methyl-threonine; 2-Butenyl-4-methylthreonine

C9H17NO3 (187.1208)

4-Hydroxy-3-nitrosobenzamide

C7H6N2O3 (166.0378)

3-Amino-4-hydroxybenzoic acid

C7H7NO3 (153.0426)

3-Amino-4-hydroxybenzoic acid is an endogenous metabolite.

Yemenine A

O-Demethylcrinamine 3-acetate

C18H19NO5 (329.1263)

Crinamidine

C17H19NO5 (317.1263)

Fe(CN)3

Fe(CN)3; Ferric cyanide; Iron cyanide (Fe(CN)3)

C3FeN3 (133.9442)

Homochelidonine

(+/-)-Homochelidonine

C21H23NO5 (369.1576)

Cyclohexyl acetate

Cyclohexyl ester OF acetic acid

C8H14O2 (142.0994)

Cyclohexyl acetate, also known as adronal acetate, belongs to the class of organic compounds known as carboxylic acid esters. These are carboxylic acid derivatives in which the carbon atom from the carbonyl group is attached to an alkyl or an aryl moiety through an oxygen atom (forming an ester group). Cyclohexyl acetate is a sweet, ethereal, and fruity tasting compound. Cyclohexyl acetate has been detected, but not quantified, in several different foods, such as brassicas, onion-family vegetables, pulses, and soy beans. Cyclohexyl acetate is a flavouring agent. It is found in many foods, some of which are pulses, soy bean, brassicas, and onion-family vegetables.

Tetracenomycin A2

C23H18O8 (422.1002)

Tetracenomycin B2

8-Demethyltetracenomycin A2

C22H16O8 (408.0845)

8-Demethyltetracenomycin C

C22H18O11 (458.0849)

A member of the class of tetracenes that is tetracenomycin C in which the methoxy group at position 3 is replaced by a phenolic OH.

Spiramycin II

acetylspiramycin

C45H76N2O15 (884.5245)

D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D007933 - Leucomycins A macrolide antibiotic produced by various Streptomyces species. Same as: D02420

Tribromobisphenol A

2,6-dibromo-4-[1-(3-bromo-4-hydroxyphenyl)-1-methylethyl]phenol

C15H13Br3O2 (461.8466)

Dibromobisphenol A

3,3-Dibromobisphenol A

C15H14Br2O2 (383.936)

Thio-THIP

Thio-4,5,6,7-tetrahydroisoxazolo(5,4-c)pyridin-3-ol

C6H8N2OS (156.0357)

m-Cresotic acid

2-Hydroxy-4-methylbenzoic acid

C8H8O3 (152.0473)

A monohydroxybenzoic acid consisting of salicylic acid having a methyl group at the 4-position.

Sulfoacetic acid

2-Sulphoacetic acid

C2H4O5S (139.9779)

2-Benzothiazolesulfonamide

1,3-Benzothiazole-2-sulfonamide

C7H6N2O2S2 (213.9871)

m-Benzenedisulfonamide

benzene-1,3-disulfonamide

C6H8N2O4S2 (235.9925)

2,2',4,4',6,6'-Hexachlorobiphenyl

1,3,5-trichloro-2-(2,4,6-trichlorophenyl)benzene

C12H4Cl6 (357.8444)

D004785 - Environmental Pollutants > D011078 - Polychlorinated Biphenyls

3-Deoxyestradiol

3-Deoxy-17beta-estradiol

C18H24O (256.1827)

2,4'-Dichlorobiphenyl

1-chloro-4-(2-chlorophenyl)benzene

C12H8Cl2 (222.0003)

D004785 - Environmental Pollutants > D011078 - Polychlorinated Biphenyls

4,4-PCB

4,4-Dichlorobiphenyl

C12H8Cl2 (222.0003)

D004785 - Environmental Pollutants > D011078 - Polychlorinated Biphenyls

5-Nitrofurfural

5-NITRO-2-FURALDEHYDE

C5H3NO4 (141.0062)

Diphenolic acid

4,4-Bis(4-hydroxyphenyl)pentanoic acid

C17H18O4 (286.1205)

ZR-515

(E,E)-1-Methylethyl 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoate

C19H34O3 (310.2508)

Same as: D08200

2,3,4-Trichlorobiphenyl

1,2,3-trichloro-4-phenylbenzene

C12H7Cl3 (255.9613)

4-Butylphenol

p-Hydroxybutylbenzene

C10H14O (150.1045)

Bolasterone

(1S,2R,9R,10R,11S,14S,15S)-14-hydroxy-2,9,14,15-tetramethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-6-en-5-one

C21H32O2 (316.2402)

Bolasterone is an anabolic androgenic steroid. Analysis of steroids in urine has been used to detect different hormonal actions in human beings such as testicular function in men, hyperandrogenic disorders in women and puberty problems in children, by the measurement of anabolic steroids, and some hormonal disorders such as adrenocortical adenoma and Cushing syndrome by the control of corticoids. This steroid have been included in the International Olympic Committee (IOC) doping list due to their illegal use in some sports and in the list of schedules drugs in several countries because of its use by young people. In addition, the examination of endogenous steroids profile provides information about the health and the use of exogenous steroids. Bolasterone is excreted as the original compound in human urine. Androgenic anabolic steroids (AAS) are defined as natural, synthetic or semi-synthetic drugs chemicals derived from testosterone, used with the aim to improve physical performance by increasing both muscle strength and mass. Despite their reported toxicological effects on the cardiovascular, hepatic and neuro-endocrine systems, the AAS have been extensively used in sports activities. The use of anabolic steroids was banned by the International Olympic Committee for the first time at the Olympic Games in Montreal in 1976. Since that time the misuse of anabolic steroids by athletes has been controlled by analysis of urine of the excreted steroids or their metabolites, or both. (PMID: 10892583, 10932808, 14976846, 15042372, 15231229, 3308301, 8456050, 8674183, 16040239) [HMDB] Bolasterone is an anabolic androgenic steroid. Analysis of steroids in urine has been used to detect different hormonal actions in human beings such as testicular function in men, hyperandrogenic disorders in women and puberty problems in children, by the measurement of anabolic steroids, and some hormonal disorders such as adrenocortical adenoma and Cushing syndrome by the control of corticoids. This steroid have been included in the International Olympic Committee (IOC) doping list due to their illegal use in some sports and in the list of schedules drugs in several countries because of its use by young people. In addition, the examination of endogenous steroids profile provides information about the health and the use of exogenous steroids. Bolasterone is excreted as the original compound in human urine. Androgenic anabolic steroids (AAS) are defined as natural, synthetic or semi-synthetic drugs chemicals derived from testosterone, used with the aim to improve physical performance by increasing both muscle strength and mass. Despite their reported toxicological effects on the cardiovascular, hepatic and neuro-endocrine systems, the AAS have been extensively used in sports activities. The use of anabolic steroids was banned by the International Olympic Committee for the first time at the Olympic Games in Montreal in 1976. Since that time the misuse of anabolic steroids by athletes has been controlled by analysis of urine of the excreted steroids or their metabolites, or both. (PMID: 10892583, 10932808, 14976846, 15042372, 15231229, 3308301, 8456050, 8674183, 16040239). D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones > D045930 - Anabolic Agents C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C2360 - Anabolic Steroid Same as: D03144

Didecyl phthalate

1,2-bis(decyl) benzene-1,2-dicarboxylate

C28H46O4 (446.3396)

Esprocarb

C15H23NOS (265.15)

1,2,4,5-Tetramethylbenzene

1,2,4,5-TETRAMETHYLBENZENE

C10H14 (134.1095)

Flavouring compound [Flavornet]

Karphos

ISOXATHION

C13H16NO4PS (313.0538)

CONFIDENCE standard compound; INTERNAL_ID 790; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9696; ORIGINAL_PRECURSOR_SCAN_NO 9695 CONFIDENCE standard compound; INTERNAL_ID 790; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9735; ORIGINAL_PRECURSOR_SCAN_NO 9730 CONFIDENCE standard compound; INTERNAL_ID 790; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9644; ORIGINAL_PRECURSOR_SCAN_NO 9642 CONFIDENCE standard compound; INTERNAL_ID 790; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9682; ORIGINAL_PRECURSOR_SCAN_NO 9680 CONFIDENCE standard compound; INTERNAL_ID 790; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9725; ORIGINAL_PRECURSOR_SCAN_NO 9724 CONFIDENCE standard compound; INTERNAL_ID 790; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9709; ORIGINAL_PRECURSOR_SCAN_NO 9708

3-Methoxy-17-epiestriol

3-Methoxyestra-1,3,5(10)-triene-16alpha,17alpha-diol

C19H26O3 (302.1882)

G - Genito urinary system and sex hormones > G03 - Sex hormones and modulators of the genital system > G03G - Gonadotropins and other ovulation stimulants > G03GB - Ovulation stimulants, synthetic D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones > D004967 - Estrogens C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C483 - Therapeutic Estrogen Same as: D04021

Drostanolone

(1S,2S,4R,7S,10R,11S,14S,15S)-14-hydroxy-2,4,15-trimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-one

C20H32O2 (304.2402)

Drostanolone is only found in individuals that have used or taken this drug. It is a potent synthetic androgenic anabolic steroid similar to testosterone. Drostanolone is indicated in postmenopausal women with recurrent breast cancer, in a combined hormone therapy.Dromostanolone is a synthetic androgenic anabolic steroid and is approximately 5 times as potent as natural methyltestosterone. Like testosterone and other androgenic hormones, dromostanolone binds to the androgen receptor. This causes downstream genetic transcriptional changes. This ultimately causes retention of nitrogen, potassium, and phosphorus; increases protein anabolism; and decreases amino acid catabolism. The antitumour activity of dromostanolone appears related to reduction or competitive inhibition of prolactin receptors or estrogen receptors or production. C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C2360 - Anabolic Steroid

Solvent Orange 3

Chrysoidine free base

C12H12N4 (212.1062)

Androstane-3,17-diol dipropionate

Androstane-3,17-diol dipropionate; 5alpha-Androstane-3alpha,17beta-diol dipropionate

C25H40O4 (404.2926)

D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones

1-nitrosonaphthalene

1-Nitrosonaphthalene

C10H7NO (157.0528)

1-nitrosonaphthalene is considered to be practically insoluble (in water) and basic

1-Nitro-7-hydroxy-8-glutathionyl-7,8-dihydronaphthalene

(2S)-2-amino-4-{[(1R)-1-[(carboxymethyl)-C-hydroxycarbonimidoyl]-2-[(2-hydroxy-8-nitro-1,2-dihydronaphthalen-1-yl)sulfanyl]ethyl]-C-hydroxycarbonimidoyl}butanoic acid

C20H24N4O9S (496.1264)

This compound belongs to the family of Peptides. These are compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another.

1-Nitro-5-glutathionyl-6-hydroxy-5,6-dihydronaphthalene

(2S)-2-amino-4-{[(1R)-1-[(carboxymethyl)-C-hydroxycarbonimidoyl]-2-[(2-hydroxy-5-nitro-1,2-dihydronaphthalen-1-yl)sulfanyl]ethyl]-C-hydroxycarbonimidoyl}butanoic acid

C20H24N4O9S (496.1264)

2,2-Dichloroacetaldehyde

α,α-dichloroacetaldehyde

C2H2Cl2O (111.9483)

This compound belongs to the family of Enolates. These are salts of enols (or of the tautomeric aldehydes or ketones), in which the anionic charge is delocalized over oxygen and carbon, or similar covalent metal derivatives in which the metal is bound to oxygen.

S-[2-(N7-Guanyl)ethyl]-N-acetyl-L-cysteine

C12H16N6O4S (340.0954)

2alpha-Methylandrosterone

3alpha-Hydroxy-2alpha-methyl-5alpha-androstan-17-one

C20H32O2 (304.2402)

16beta-Estradiol

13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,16-diol

C18H24O2 (272.1776)

D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones

Fluoroacetaldehyde

2-fluoroacetaldehyde

C2H3FO (62.0168)

4a-Hydroxytetrahydrobiopterin

(4aS,6R)-2-amino-6-[(1R,2S)-1,2-dihydroxypropyl]-4a-hydroxy-4,4a,5,6,7,8-hexahydropteridin-4-one

C9H15N5O4 (257.1124)

Tetrahydrobiopterin (BH4) is essential for catalyzing the conversion of phenylalanine into tyrosine by phenylalanine hydroxylase. During this physiological reaction, the oxidation of BH4 creates 4a-hydroxytetrahydropterin (CAS: 70110-58-6) intermediates and hydrogen peroxide is formed. The hydrogen peroxide and the hydroxytetrahydropterin can both be derived from alternate breakdown routes of a common precursor, the corresponding 4a-hydroperoxytetrahydropterin (PMID: 8323303). Tetrahydrobiopterin (BH4) is essential to catalyze the conversion of phenylalanine to tyrosine by phenylalanine hydroxylase. During this physiological reaction, the oxidation of BH4 creates 4a-hydroxytetrahydropterin intermediates and hydrogen peroxide is formed. The hydrogen peroxide and the hydroxytetrahydropterin can both derive from alternate routes of breakdown of a common precursor, the corresponding 4a-hydroperoxytetrahydropterin. (PMID 8323303) [HMDB]

Pyoverdine I

Pyoverdin Pa A

C55H83N17O22 (1333.5898)

Coelichelin

C21H39N7O11 (565.2707)

A tetrapeptide hydroxamate siderophore that is isolated from Streptomyces coelicolor.

Hydroxyspheroidene

3,4-Didehydro-1,1,2,2,7,8-hexahydro-1-hydroxy-1-methoxy-psi,psi-carotene

C41H62O2 (586.475)

D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids

leucokininI

Leucokinin I

C41H53N11O12 (891.3875)

6-(alpha-D-Glucosaminyl)-1D-myo-inositol 1,2-cyclic phosphate

C12H22NO12P (403.088)

A myo-inositol cyclic phosphate that is 1D-myo-inositol 1,2-cyclic phosphate having an alpha-D-glucosaminyl residue attached at the 6-position.

3-hydroxyoctadecanoyl-CoA

{[5-(6-amino-9H-purin-9-yl)-4-hydroxy-2-({[hydroxy({[hydroxy(3-hydroxy-3-{[2-({2-[(3-hydroxyoctadecanoyl)sulfanyl]ethyl}carbamoyl)ethyl]carbamoyl}-2,2-dimethylpropoxy)phosphoryl]oxy})phosphoryl]oxy}methyl)oxolan-3-yl]oxy}phosphonic acid

C39H70N7O18P3S (1049.3711)

3-hydroxyoctadecanoyl-CoA is a human metabolite involved in the fatty acid elongation in mitochondria pathway. The enzyme long-chain-3-hydroxyacyl-CoA dehydrogenase catalyzes the conversion of 3-Oxododecanoyl-CoA to (S)-3-Hydroxydodecanoyl-CoA.3-hydroxyoctadecanoyl-CoA is an intermediate in fatty acid metabolism, being the substrate of the enzymes beta-hydroxyacyl-CoA dehydrogenase and 3-hydroxyacyl-CoA dehydrogenase [EC 1.1.1.211-1.1.1.35]; 3-hydroxyoctadecanoyl-CoA is an intermediate in fatty acid elongation in mitochondria, the substrate of the enzymes enoyl-CoA hydratase and long-chain-enoyl-CoA hydratase [EC 4.2.1.17-4.2.1.74]. (KEGG).

6alpha-Hydroxymaackiain

5,7,11,19-tetraoxapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2,4(8),9,13(18),14,16-hexaene-1,16-diol

C16H12O6 (300.0634)

Isolated from leaves of Trifolium pratense (red clover) as a phytoalexin. 6alpha-Hydroxymaackiain is found in many foods, some of which are pulses, tea, common pea, and herbs and spices. 6alpha-Hydroxymaackiain is found in common pea. 6alpha-Hydroxymaackiain is isolated from leaves of Trifolium pratense (red clover) as a phytoalexin.

Petromyzonol

3α,7α,12α,24-tetrahydroxy-5α-cholane

C24H42O4 (394.3083)

2,3-Dihydroxy-2-carboxybiphenyl

C13H10O4 (230.0579)

Thiobenzamide S-oxide

Phenyl(sulphinylidene)methanamine

C7H7NOS (153.0248)

Volicitin

N-(17-hydroxy-9Z,12Z,15Z-octadecatrienoyl) glutamine

C23H38N2O5 (422.2781)

Fructoselysine 6-phosphate

C12H25N2O10P (388.1247)

An L-lysine derivative having a 6-phosphofructosyl group attached to the side-chain amino group.

15Z-tetracosenoyl-CoA

{[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-2-({[hydroxy({hydroxy[(3R)-3-hydroxy-2,2-dimethyl-3-{[2-({2-[(15Z)-tetracos-15-enoylsulfanyl]ethyl}carbamoyl)ethyl]carbamoyl}propoxy]phosphoryl}oxy)phosphoryl]oxy}methyl)oxolan-3-yl]oxy}phosphonic acid

C45H80N7O17P3S (1115.4544)

15z-tetracosenoyl-coa, also known as nervonoyl-coa, is a member of the class of compounds known as very long-chain fatty acyl coas. Very long-chain fatty acyl coas are acyl CoAs where the group acylated to the coenzyme A moiety is a very long aliphatic chain of 22 carbon atoms or more. Thus, 15z-tetracosenoyl-coa is considered to be a fatty ester lipid molecule. 15z-tetracosenoyl-coa is practically insoluble (in water) and an extremely strong acidic compound (based on its pKa). 15z-tetracosenoyl-coa can be found in a number of food items such as hazelnut, sugar apple, cardamom, and ginkgo nuts, which makes 15z-tetracosenoyl-coa a potential biomarker for the consumption of these food products. In humans, 15z-tetracosenoyl-coa is involved in several metabolic disorders, some of which include de novo triacylglycerol biosynthesis TG(24:1(15Z)/22:4(7Z,10Z,13Z,16Z)/18:3(6Z,9Z,12Z)), de novo triacylglycerol biosynthesis TG(24:1(15Z)/22:1(13Z)/20:5(5Z,8Z,11Z,14Z,17Z)), de novo triacylglycerol biosynthesis TG(20:0/24:1(15Z)/20:4(5Z,8Z,11Z,14Z)), and de novo triacylglycerol biosynthesis TG(24:0/22:2(13Z,16Z)/24:1(15Z)). 15Z-tetracosenoyl-CoA is classified as a member of the Very long-chain fatty acyl CoAs. Very long-chain fatty acyl CoAs are acyl CoAs where the group acylated to the coenzyme A moiety is a very long aliphatic chain of 22 carbon atoms or more. 15Z-tetracosenoyl-CoA is considered to be practically insoluble (in water) and acidic. 15Z-tetracosenoyl-CoA is a fatty ester lipid molecule

Alcophosphamide

3-({amino[bis(2-chloroethyl)amino]phosphoryl}oxy)propan-1-ol

C7H17Cl2N2O3P (278.0354)

Detoxification of cyclophosphamide is effected, in part, by hepatic class 1 aldehyde dehydrogenase (ALDH-1)-catalyzed oxidation of aldophosphamide, a pivotal aldehyde intermediate, to the nontoxic metabolite, carboxyphosphamide. Detoxification of aldophosphamide may also be effected by enzymes, viz. Thus, NAD-linked oxidation and NADPH-linked reduction of aldophosphamide catalyzed by relevant erythrocyte enzymes were quantified. (PMID: 9394035) It has already been demonstrated that horse liver alcohol dehydrogenase catalyzes the reduction of aldophosphamide to alcophosphamide. (PMID: 8216347) D000970 - Antineoplastic Agents > D018906 - Antineoplastic Agents, Alkylating > D009588 - Nitrogen Mustard Compounds D000970 - Antineoplastic Agents > D018906 - Antineoplastic Agents, Alkylating > D010752 - Phosphoramide Mustards

7-Oxoheptanoic acid

7-Ketoheptanoic acid

C7H12O3 (144.0786)

6-Thiourate

6-thio- (van) (8CI) uric acid

C5H4N4O2S (184.0055)

This compound belongs to the family of Purines and Purine Derivatives. These are aromatic heterocyclic compounds containing a purine moiety, which is formed a pyrimidine-ring ring fused to an imidazole ring.

2-ene-Valproic acid

2-Propyl-2-pentenoic acid, sodium salt

C8H14O2 (142.0994)

2-ene-Valproic acid is only found in individuals that have used or taken Valproic Acid.2-ene-Valproic acid is a metabolite of Valproic Acid. 2-ene-valproic acid belongs to the family of Branched Fatty Acids. These are fatty acids containing a branched chain. D002491 - Central Nervous System Agents > D000927 - Anticonvulsants D009676 - Noxae > D013723 - Teratogens

7-Aminomethyl-7-carbaguanine

2-amino-5-(aminomethyl)-3H,4H,7H-pyrrolo[2,3-d]pyrimidin-4-one

C7H9N5O (179.0807)

7-Aminomethyl-7-carbaguanine is one of the precursors of nucleoside Q (queuosine) biosynthesis. It is a substrate for preQ1 synthase (EC 1.7.1.13) which catalyzes the NADPH-dependent reduction of 7-cyano-7-carbaguanine (preQ0) to 7-aminomethyl-7-carbaguanine (preQ1). More specifically, this enzyme catalyzes the chemical reaction. 7-aminomethyl-7-carbaguanine + 2 NADP+ <-> 7-cyano-7-carbaguanine + 2 NADPH + 2 H+. 7-Aminomethyl-7-carbaguanine is one of the precursors of nucleoside Q (queuosine) biosynthesis. It is a substrate for preQ1 synthase (EC 1.7.1.13) which catalyzes the NADPH-dependent reduction of 7-cyano-7-carbaguanine (preQ0) to 7-aminomethyl-7-carbaguanine (preQ1). More specifically, this enzyme catalyzes the chemical reaction

Hydnocarpic acid

11-[(1R)-cyclopent-2-en-1-yl]undecanoic acid

C16H28O2 (252.2089)

An optically active form of hydnocarpic acid having (R)-configuration. A cyclopentenyl fatty acid consisting of undecanoic acid having a cyclopent-2-enyl group at the 11-position.

Ophiobolene

Ophiobolin F; Ophiobolene

C25H42O (358.3235)

A sesterterpenoid that is (7Z)-ophiobola-7,19-diene carrying a hydroxy substituent at position 3.

Eucarvone

2,4-Cycloheptadien-1-one,2,6,6-trimethyl-

C10H14O (150.1045)

Eucarvone is a member of the class of compounds known as monocyclic monoterpenoids. Monocyclic monoterpenoids are monoterpenoids containing 1 ring in the isoprene chain. Eucarvone is slightly soluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Eucarvone can be found in blackcurrant, which makes eucarvone a potential biomarker for the consumption of this food product.

2-(2-Methylthio)ethylmalate

2-(2-Methylthio)ethylmalic acid

C7H12O5S (208.0405)

dihomomethionine

(S)-2-Amino-6-(methylthio)hexanoic acid

C7H15NO2S (177.0823)

A sulfur-containing amino acid consisting of 2-aminohexanoic acid having a methylthio substituent at the 6-position.

7 alpha,26-Dihydroxy-4-cholesten-3-one

(2R,9R,15R)-9-hydroxy-14-[(2R)-7-hydroxy-6-methylheptan-2-yl]-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-6-en-5-one

C27H44O3 (416.329)

7 alpha,26-Dihydroxy-4-cholesten-3-one is involved in primary bile acid biosynthesis. 7 alpha,26-Dihydroxy-4-cholesten-3-one is produced from 7 alpha,27-Dihydroxycholesterol through the action of HSD3B7 (EC:1.1.1.181). 7 alpha,26-Dihydroxy-4-cholesten-3-one can then be converted to 7 alpha-Hydroxy-3-oxo-4-cholestenoate by CYP27A (EC:1.14.13.15). 7 alpha,26-Dihydroxy-4-cholesten-3-one is involved in primary bile acid biosynthesis.

Pellidole

Diacetylaminoazotoluene

C18H19N3O2 (309.1477)

Germacrone 4,5-epoxide

(6Z)-6,10-dimethyl-3-(propan-2-ylidene)-11-oxabicyclo[8.1.0]undec-6-en-4-one

C15H22O2 (234.162)

Germacrone 4,5-epoxide is found in turmeric. Germacrone 4,5-epoxide is a constituent of essential oil of Curcuma zedoaria (zedoary) Constituent of essential oil of Curcuma zedoaria (zedoary). Germacrone 4,5-epoxide is found in turmeric.

gamma-Terpineol

1-Methyl-4-(1-methylethylidene)cyclohexanol, 9ci

C10H18O (154.1358)

gamma-Terpineol is found in ceylan cinnamon. gamma-Terpineol is isolated from carrot oils, from the cinnamon tree (Cinnamomum zeylanicum) and Scotch pine (Pinus sylvestris).Terpineol is a naturally occurring monoterpene alcohol that has been isolated from a variety of sources such as cajuput oil, pine oil, and petitgrain oil. There are three isomers, alpha-, beta-, and gamma-terpineol, the last two differing only by the location of the double bond. Terpineol is usually a mixture of these isomers with alpha-terpineol as the major constituent. (Wikipedia). Isolated from carrot oils, from the cinnamon tree (Cinnamomum zeylanicum) and Scotch pine (Pinus sylvestris)

Butirosin

butirosin A

C21H41N5O12 (555.2752)

D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents

8-oxogeranial

2,6-Octadienedial, 2,6-dimethyl-, (E,E)-

C10H14O2 (166.0994)

Procyanidin B5

(2S)-2-(3,4-dihydroxyphenyl)-6-[(2R,3R,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-4-yl]-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

C30H26O12 (578.1424)

Isolated from cacao Theobroma cacao. Procyanidin B5 is found in many foods, some of which are medlar, red bell pepper, red raspberry, and apricot. Procyanidin B5 is found in apple. Procyanidin B5 is isolated from cacao Theobroma cacao.

JI-20A

Antibiotic JI-20A

C19H39N5O9 (481.2748)

D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D005839 - Gentamicins

3,3-Diethyl-2,4-dioxopiperidine

C9H15NO2 (169.1103)

R - Respiratory system > R05 - Cough and cold preparations > R05D - Cough suppressants, excl. combinations with expectorants C78273 - Agent Affecting Respiratory System > C66917 - Antitussive Agent

Senegin IV

C81H122O39 (1718.7563)

Atractylodinol

(2E,8E)-9-(Furan-2-yl)nona-2,8-dien-4,6-diyn-1-ol

C13H10O2 (198.0681)

SF-2052

Formimidoyl-fortimicin A

C18H36N6O6 (432.2696)

5alpha-Pregnan-20alpha-ol-3-one

(1S,2S,7S,10R,11S,14S,15S)-14-[(1S)-1-hydroxyethyl]-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-one

C21H34O2 (318.2559)

This compound belongs to the family of Gluco/mineralocorticoids, Progestogins and Derivatives. These are steroids whose structure is based on an hydroxylated prostane moiety.

alpha-cis-bergamotene

(1R,5R)-2,6-dimethyl-6-(4-methylpent-3-enyl)bicyclo[3.1.1]hept-2-ene

C15H24 (204.1878)

Leucocyanidin

(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,4,5,7-tetrol

C15H14O7 (306.0739)

Leucocyanidin is a leucoanthocyanidin. Leucocyanidin is a natural product found in Euphorbia hirta, Koenigia coriaria, and Cassia roxburghii with data available. Leucocyanidin is an active anti-ulcerogenic ingredient was extracted from Litchi Chinensis. Leucocyanidin demonstrates a significant protective effect against Aspirin-induced erosions in rat models[1]. Leucocyanidin is an active anti-ulcerogenic ingredient was extracted from Litchi Chinensis. Leucocyanidin demonstrates a significant protective effect against Aspirin-induced erosions in rat models[1].

18R-HEPE

(5Z,8Z,11E,14Z,16E,18S)-18-hydroxyicosa-5,8,11,14,16-pentaenoic acid

C20H30O3 (318.2195)

18R-HEPE which is the R form of 18(+/-)-HEPE, is produced by non-enzymatic oxidation of EPA. [HMDB] 18R-HEPE which is the R form of 18(+/-)-HEPE, is produced by non-enzymatic oxidation of EPA.

Calusterone

(1S,2R,9S,10R,11S,14S,15S)-14-hydroxy-2,9,14,15-tetramethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-6-en-5-one

C21H32O2 (316.2402)

Calusterone is an androgenic steroid. Calusterone induce given orally induce a marked decrease (between 30 and 70\\% depending on the dose) in the binding capacity of oestradiol-17beta to specific uterine receptors in vivo. As an androgen, calusterone has been used as a therapeutic agent in postmenopausal women with metastatic breast cancer; the addition of a potent hormonal agent to effective cytotoxic chemotherapy improves the results of treatment of women with metastatic breast cancer. Calusterone is tested in sport screening; fast and sensitive method for the comprehensive screening of anabolic agents and other banned doping substances using gas chromatography/tandem mass spectrometry (GC/MS/MS) with an external ionization ion trap mass spectrometer have been developed for the parent substances and their metabolites. (PMID: 17610244, 12375280, 153787, 2325376, 12375280) [HMDB] Calusterone is an androgenic steroid. Calusterone induce given orally induce a marked decrease (between 30 and 70\\% depending on the dose) in the binding capacity of oestradiol-17beta to specific uterine receptors in vivo. As an androgen, calusterone has been used as a therapeutic agent in postmenopausal women with metastatic breast cancer; the addition of a potent hormonal agent to effective cytotoxic chemotherapy improves the results of treatment of women with metastatic breast cancer. Calusterone is tested in sport screening; fast and sensitive method for the comprehensive screening of anabolic agents and other banned doping substances using gas chromatography/tandem mass spectrometry (GC/MS/MS) with an external ionization ion trap mass spectrometer have been developed for the parent substances and their metabolites. (PMID: 17610244, 12375280, 153787, 2325376, 12375280). D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones > D045930 - Anabolic Agents C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C2360 - Anabolic Steroid Same as: D03144

Nervonyl CoA

(2S)-4-({[({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)-2-hydroxy-3,3-dimethyl-N-[2-({2-[(15Z)-tetracos-15-enoylsulfanyl]ethyl}-C-hydroxycarbonimidoyl)ethyl]butanimidic acid

C45H80N7O17P3S (1115.4544)

This compound belongs to the family of Acyl CoAs. These are organic compounds contaning a coenzyme A substructure linked to another moeity through an ester bond.

L-Dopaquinone

2-amino-3-(3,4-dioxocyclohexa-1,5-dien-1-yl)propanoic acid

C9H9NO4 (195.0532)

Implicated in food discolouration (enzymatic browning). Implicated in food discolouration (enzymatic browning)

(13S)-13-hydroxyoctadeca-9,11-dienoic acid

13-Hydroxy-9,11-octadecadienoic acid, (S)-(e,Z)-isomer

C18H32O3 (296.2351)

1,2-Dichloroethylene

1,2-Dichloroethylene, (e)-isomer

C2H2Cl2 (95.9534)

2-Amino-4-oxopentanoic acid

C5H9NO3 (131.0582)

2,4-Diaminoazobenzene

4-(2-phenyldiazen-1-yl)benzene-1,3-diamine

C12H12N4 (212.1062)

2,4-Dodecadienoic acid, 11-methoxy-3,7,11-trimethyl-, 1-methylethyl ester, (2Z,4E,7S)-

C19H34O3 (310.2508)

Octadeca-6,9,12,15-tetraenoic acid

octadeca-6,9,12,15-tetraenoic acid

C18H28O2 (276.2089)

Octadeca-6,9,12,15-tetraenoic acid, also known as 6,9,12,15-octadecatetraenoic acid, belongs to lineolic acids and derivatives class of compounds. Those are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions. Octadeca-6,9,12,15-tetraenoic acid is practically insoluble (in water) and a weakly acidic compound (based on its pKa). Octadeca-6,9,12,15-tetraenoic acid can be found in borage, which makes octadeca-6,9,12,15-tetraenoic acid a potential biomarker for the consumption of this food product.

[(1r)-1-Aminoethyl]phosphonic acid

1-(Aminoethyl)phosphonic acid, (+-)-isomer

C2H8NO3P (125.0242)

BENZOYLARGININE NITROANILIDE

5-[(diaminomethylidene)amino]-N-(4-nitrophenyl)-2-(phenylformamido)pentanamide

C19H22N6O4 (398.1702)

D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D002863 - Chromogenic Compounds D004396 - Coloring Agents

Dactimicin

N-(4-amino-3-{[3-amino-6-(1-aminoethyl)oxan-2-yl]oxy}-2,5-dihydroxy-6-methoxycyclohexyl)-2-methanimidamido-N-methylacetamide

C18H36N6O6 (432.2696)

Diacetazotol

N-acetyl-N-{2-methyl-4-[2-(2-methylphenyl)diazen-1-yl]phenyl}acetamide

C18H19N3O2 (309.1477)

4-Aminohex-5-ynoic acid

4-Amino-5-hexynoic acid

C6H9NO2 (127.0633)

D004791 - Enzyme Inhibitors

Levopromazine

[3-(2-methoxy-10H-phenothiazin-10-yl)-2-methylpropyl]dimethylamine

C19H24N2OS (328.1609)

D002492 - Central Nervous System Depressants > D014149 - Tranquilizing Agents > D014150 - Antipsychotic Agents D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D014149 - Tranquilizing Agents D018377 - Neurotransmitter Agents > D015259 - Dopamine Agents > D018492 - Dopamine Antagonists D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics

N-acetyl Leukotriene E4

6-({2-carboxy-2-[(1-hydroxyethylidene)amino]ethyl}sulphanyl)-5-hydroxyicosa-7,9,11,14-tetraenoic acid

C25H39NO6S (481.2498)

Leucocyanidin

2-(3,4-Dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,4,5,7-tetrol

C15H14O7 (306.0739)

Leucocyanidin, also known as 3,3,4,4,5,7-flavanhexol or resivit, is a member of the class of compounds known as catechins. Catechins are compounds containing a catechin moiety, which is a 3,4-dihydro-2-chromene-3,5.7-tiol. Thus, leucocyanidin is considered to be a flavonoid lipid molecule. Leucocyanidin is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Leucocyanidin can be found in a number of food items such as climbing bean, black mulberry, corn salad, and caraway, which makes leucocyanidin a potential biomarker for the consumption of these food products. Leucocyanidin is a colorless chemical compound that is a member of the class of natural products known as leucoanthocyanidins . Leucocyanidin is an active anti-ulcerogenic ingredient was extracted from Litchi Chinensis. Leucocyanidin demonstrates a significant protective effect against Aspirin-induced erosions in rat models[1]. Leucocyanidin is an active anti-ulcerogenic ingredient was extracted from Litchi Chinensis. Leucocyanidin demonstrates a significant protective effect against Aspirin-induced erosions in rat models[1].

alpha-fenchyl alcoholalpha-1,3,3-trimethyl-norbornan-2-ol

C10H18O (154.1358)

Fenchol or 1,3,3-Trimethylbicyclo[2.2.1]heptan-2-ol, belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. Fenchol is a naturally occurring bicyclic monoterpenoid and an isomer of Borneol. Monoterpenoids are terpenes that contain 10 carbon atoms and are comprised of two isoprene units. The biosynthesis of monoterpenes is known to occur mainly through the methyl-eritritol-phosphate (MEP) pathway in the plastids. Geranyl diphosphate (GPP) is a key intermediate in the biosynthesis of cyclic monoterpenes. GPP undergoes several cyclation reactions to yield a diverse number of cyclic arrangements. Fenchol is an extremely weak basic (essentially neutral) compound (based on its pKa). It is a colorless or white solid with a characteristic scent found in basil and Aster. Fenchol is used extensively in perfumery. Flavouring compound [Flavornet]

N-ACETYLANTHRANILIC ACID

N-Acetyl-anthranilic acid

C9H9NO3 (179.0582)

Pseudobaptigenin

3- (1,3-Benzodioxol-5-yl) -7-hydroxy-4H-1-benzopyran-4-one

C16H10O5 (282.0528)

A member of the class of 7-hydroxyisoflavones that is 7-hydroxyisoflavone and in which the phenyl group at position 3 is replaced by a 1,3-benzodioxol-5-yl group.

TRANS-3-CHLOROACRYLIC ACID

(2E)-3-Chloro-2-propenoic acid

C3H3ClO2 (105.9822)

Isogentisin

1,3-Dihydroxy-7-methoxyxanthone

C14H10O5 (258.0528)

A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1 and 3 and a methoxy group at position 7.

NCI60_026742

4H-1-Benzopyran-4-one, 5,6,7,8-tetramethoxy-2-(3,4,5-trimethoxyphenyl)-

C22H24O9 (432.142)

2-(3,4,5-trimethoxyphenyl)-5,6,7,8-tetramethoxy-4H-1-benzopyran-4-one is a methoxyflavone that is flavone substituted by methoxy groups at positions 5, 6, 7, 8, 3, 4 and 5. It has a role as a plant metabolite. It is functionally related to a flavone. 5,6,7,8,3,4,5-Heptamethoxyflavone is a natural product found in Conoclinium coelestinum, Citrus medica, and other organisms with data available.

ACon1_000409

5-[4-Carboxy-2-[[1,3-dioxo-3-[4-[(1-oxooctadecyl)-amino]phenyl]propyl]amino]phenoxy]isophthalicacid

C15H12O6 (288.0634)

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-4-one is a member of flavanones. (+/-)-Eriodictyol is a natural product found in Prunus campanulata, Lawsonia inermis, and other organisms with data available.

ST 29:3;O

(3S,5S,9R,10S,13R,14R,17R)-17-[(2R,3E,5R)-5-ethyl-6-methylhepta-3,6-dien-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

C29H46O (410.3548)

A 3beta-sterol that is methyl-5alpha-ergosta-8,14,24(28)-trien-3beta-ol carrying an additional 4alpha-methyl substituent. Stigmasta-7,22E,25-trien-3beta-ol is a steroid. It derives from a hydride of a stigmastane.

Benzoylecgonine

(3S,4R)-3-benzoyloxy-8-methyl-8-azabicyclo[3.2.1]octane-4-carboxylic acid

C16H19NO4 (289.1314)

CONFIDENCE standard compound; EAWAG_UCHEM_ID 2823

Cephalomannine

[(1S,2S,3R,4S,7R,9R,10S,12S,15S)-4,12-diacetyloxy-1,9-dihydroxy-15-[(2R,3S)-2-hydroxy-3-[[(E)-2-methylbut-2-enoyl]amino]-3-phenylpropanoyl]oxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate

C45H53NO14 (831.3466)

relative retention time with respect to 9-anthracene Carboxylic Acid is 1.172 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.307 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.248 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.291 Cephalomannine is a Paclitaxel (HY-B0015) alkaloidal analog and isolated from most Cephalotaxus species. Cephalomannine is an orally active anti-tumor agent and can be used as a chemotherapy agent for cancer research[1][2]. Cephalomannine is a Paclitaxel (HY-B0015) alkaloidal analog that can be isolated from most Cephalotaxus species. Cephalomannine is an orally active anti-tumor agent and can be used as a chemotherapy agent for cancer research[1][2][3][4]. Cephalomannine is a Paclitaxel (HY-B0015) alkaloidal analog and isolated from most Cephalotaxus species. Cephalomannine is an orally active anti-tumor agent and can be used as a chemotherapy agent for cancer research[1][2].

Isopyridoxal

Pyridoxal hydrochrolide

C8H9NO3 (167.0582)

A pyridinecarbaldehyde that is pyridine-5-carbaldehyde bearing methyl, hydroxy and hydroxymethyl substituents at positions 2, 3 and 4 respectively.

2-Hydroxyformononetin

C16H12O5 (284.0685)

A methoxyisoflavone that is formononetin with a hydroxy group at position 2.

Melilotoside

(E)-3-[2-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]oxy]phenyl]prop-2-enoic acid

C15H18O8 (326.1002)

3-Ketocholanic acid

C24H38O3 (374.2821)

CONFIDENCE standard compound; INTERNAL_ID 76

Hippeastrine

(2S,3S,9S,10S)-9-hydroxy-4-methyl-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),7,13,15(19)-tetraen-12-one

C17H17NO5 (315.1107)

Hippeastrine is an indole alkaloid isolated from the Amaryllidaceae family and has been shown to exhibit cytotoxic activity. It has a role as an antineoplastic agent and a metabolite. It is an indole alkaloid, a delta-lactone, a secondary alcohol and an organic heteropentacyclic compound. Hippeastrine is a natural product found in Pancratium trianthum, Pancratium canariense, and other organisms with data available. An indole alkaloid isolated from the Amaryllidaceae family and has been shown to exhibit cytotoxic activity. Origin: Plant; SubCategory_DNP: Isoquinoline alkaloids, Amaryllidaceae alkaloids

Vulgarin

C15H20O4 (264.1362)

Origin: Plant; SubCategory_DNP: Sesquiterpenoids

3,4-AHBA

3-Amino-4-hydroxybenzoic acid

C7H7NO3 (153.0426)

3-Amino-4-hydroxybenzoic acid is an endogenous metabolite.

3-Amino-4-hydroxybenzoic acid

C7H7NO3 (153.0426)

3-Amino-4-hydroxybenzoic acid is an endogenous metabolite.

2-Aminobenzenesulfonic acid

C6H7NO3S (173.0147)

2-Aminobenzenesulfonic acid is an endogenous metabolite.

DICLOBUTRAZOL

Pesticide6_Diclobutrazol_C15H19Cl2N3O_1-(2,4-Dichlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)-3-pentanol

C15H19Cl2N3O (327.0905)

Eremantholide A

C19H24O6 (348.1573)

5,7,3,4,5-Pentahydroxyflavanone

C15H12O7 (304.0583)

2-Hydroxyphytanic acid

2-hydroxy-3,7,11,15-tetramethylhexadecanoic acid

C20H40O3 (328.2977)

An alpha-hydroxy fatty acid formed from phytanic acid by bacterial cytochrome P450; and also formed in human peroxisomal disorders.

3alpha,7alpha-Dihydroxy-5beta-cholestan-26-oic acid

C27H46O4 (434.3396)

A cholestanoid that is 5beta-cholestan-26-oic acid substituted by alpha-hydroxy groups at positions 3 and 7 respectively.

16-kaurene

5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadecane

C20H32 (272.2504)

L-dopaquinone

2-amino-3-(3,4-dioxocyclohexa-1,5-dien-1-yl)propanoic acid

C9H9NO4 (195.0532)

3-oxodecanoyl-CoA

C31H52N7O18P3S (935.2302)

An oxo-fatty acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxylic acid group of 3-oxodecanoic acid.

FA 5:1;O2

(4S)-4-hydroxy-2-ketovaleric acid;(4S)-4-hydroxy-2-oxovaleric acid;(S)-4-hydroxy-2-ketopentanoic acid

C5H8O4 (132.0423)

D018377 - Neurotransmitter Agents > D018847 - Opioid Peptides D018377 - Neurotransmitter Agents > D004399 - Dynorphins 2-Methylsuccinic acid is a normal metabolite in human fluids and the main biochemical measurable features in ethylmalonic encephalopathy. Ethylmalonic acid is non-carcinogenic potentially toxic and associated with anorexia nervosa and malonyl-CoA decarboxylase deficiency.

FA 16:2

11-(2-cyclopenten-1-yl)undecanoic acid

C16H28O2 (252.2089)

2-Amino-4-oxopentanoic acid

2-amino-4-oxo-pentanoic acid

C5H9NO3 (131.0582)

A derivative of valeric acid having amino and oxo substituents at the 2- and 4-positions respectively.

7,8-Diaminononanoic acid

7,8-DAP;7,8-DAPA;7,8-Diaminononanoate;7,8-diaminopelargonic acid;DAP;DAPA

C9H20N2O2 (188.1525)

An amino fatty acid carrying amino substituents at positions 7 and 8. Some of its isomers are naturally occurring intermediates of biotin synthesis, and targets of antimicrobial and herbicide development.

20-hydroxy-LTE4

5S,20-dihydroxy-6R-(S-cysteinyl),7E,9E,11Z,14Z-eicosatetraenoic acid

C23H37NO6S (455.2341)

20-Hydroxy-leukotriene E4

(5S,6R,7E,9E,11Z,14Z)-6-[(2-amino-2-carboxyethyl)sulfanyl]-5,20-dihydroxyicosa-7,9,11,14-tetraenoic acid

C23H37NO6S (455.2341)

8R-HPETE

(5Z,9E,11Z,14Z)-(8R)-8-Hydroxyperoxyeicosa-5,9,11,14-tetraenoate

C20H32O4 (336.23)

18R-HEPE

18R-hydroxy-5Z,8Z,11Z,14Z,16E-eicosapentaenoic acid

C20H30O3 (318.2195)

An 18-HEPE that consists of (5Z,8Z,11Z,14Z,16E)-icosapentaenoic in which the 18-hydroxy group has R-configuration.

CoA 20:3

(8Z,11Z,14Z)-eicosatrienoyl-coenzyme A;8Z,11Z,14Z-eicosatrienoyl-CoA;8Z,11Z,14Z-icosatrienoyl-CoA;CoA[20:3(8Z,11Z,14Z)];all-cis-eicosa-8,11,14-trienoyl-CoA;all-cis-eicosa-8,11,14-trienoyl-coenzyme A;all-cis-icosa-8,11,14-trienoyl-CoA;all-cis-icosa-8,11,14-trienoyl-coenzyme A

C41H68N7O17P3S (1055.3605)

CoA 18:0;O

3-phosphoadenosine 5-{3-[(3R)-3-hydroxy-4-{[3-({2-[(3-hydroxyoctadecanoyl)sulfanyl]ethyl}amino)-3-oxopropyl]amino}-2,2-dimethyl-4-oxobutyl] dihydrogen diphosphate}

C39H70N7O18P3S (1049.3711)

A 3-hydroxy fatty acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of 3-hydroxyoctadecanoic acid.

CoA 10:1;O

{[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-2-({[hydroxy({hydroxy[(3R)-3-hydroxy-3-{[2-({2-[(3-hydroxy-2,6-dimethyl-5-methylideneheptanoyl)sulfanyl]ethyl}carbamoyl)ethyl]carbamoyl}-2,2-dimethylpropoxy]phosphoryl}oxy)phosphoryl]oxy}methyl)oxolan-3-yl]oxy}phosphonic acid

C31H52N7O18P3S (935.2302)

anthraniloyl-CoA

3-phosphoadenosine 5-{3-[(3R)-4-{[3-({2-[(2-aminobenzoyl)sulfanyl]ethyl}amino)-3-oxopropyl]amino}-3-hydroxy-2,2-dimethyl-4-oxobutyl] dihydrogen diphosphate}

C28H41N8O17P3S (886.1523)

A member of the class of benzoyl-CoAs having 2-aminobenzoyl as the S-acyl group.

Itaconyl-CoA

3-phosphoadenosine 5-{3-[(3R)-4-{[3-({2-[(3-carboxybut-3-enoyl)sulfanyl]ethyl}amino)-3-oxopropyl]amino}-3-hydroxy-2,2-dimethyl-4-oxobutyl] dihydrogen diphosphate}

C26H40N7O19P3S (879.1312)

The S-itaconyl derivative of coenzyme A.

palmitone

hentriacontan-16-one

C31H62O (450.48)

ST 27:1;O4

(3alpha,5beta,7alpha,12alpha)-3,7,12-trihydroxycholestan-26-al

C27H46O4 (434.3396)

ST 28:4;O

(22E)-24-methylcholesta-5,7,22,24(24(1))-tetraen-3beta-ol

C28H42O (394.3235)

(+)-cis-sabinol

(1S,3R,5S)-4-methylidene-1-(propan-2-yl)bicyclo[3.1.0]hexan-3-ol

C10H16O (152.1201)

Erythromycin C

C36H65NO13 (719.4456)

An erythromycin that consists of erythronolide A having 2,6-dideoxy-3-C-methyl-alpha-L-ribo-hexopyranosyl and 3,4,6-trideoxy-3-(dimethylamino)-beta-D-xylo-hexopyranosyl residues attahced at positions 4 and 6 respectively. D004791 - Enzyme Inhibitors > D011500 - Protein Synthesis Inhibitors D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents D005765 - Gastrointestinal Agents

Xenognosin B

7-Hydroxy-3-(2-hydroxy-4-methoxyphenyl)-4H-chromen-4-one

C16H12O5 (284.0685)

7β-Eplerenone Impurity

(7beta,11alpha,17alpha)-9,11-Epoxy-17-hydroxy-3-oxo-pregn-4-ene-7,21-dicarboxylic acid gamma-lactone methyl ester

C24H30O6 (414.2042)

Protirelina

C16H22N6O4 (362.1702)

H - Systemic hormonal preparations, excl. sex hormones and insulins > H01 - Pituitary and hypothalamic hormones and analogues > H01A - Anterior pituitary lobe hormones and analogues > H01AB - Thyrotropin

17-Hydroxyandrost-4-en-3-one

C19H28O2 (288.2089)

D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones

omega-Carboxy-N-acetyl-LTE4

C25H37NO8S (511.224)

Bolasterone

17beta-hydroxy-7alpha,17-dimethylandrost-4-en-3-one

C21H32O2 (316.2402)

D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones > D045930 - Anabolic Agents C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C2360 - Anabolic Steroid Same as: D03144

Eucarvone

2,4-Cycloheptadien-1-one, 2,6,6-trimethyl-

C10H14O (150.1045)

Isoguanine

2H-Purin-2-one, 6-amino-1,3-dihydro- (9CI)

C5H5N5O (151.0494)

Prenal

InChI=1\C5H8O\c1-5(2)3-4-6\h3-4H,1-2H

C5H8O (84.0575)

Albafuran A

4-[(2E)-3,7-dimethylocta-2,6-dienyl]-5-(6-hydroxy-1-benzofuran-2-yl)benzene-1,3-diol

C24H26O4 (378.1831)

A member of the class of 1-benzofurans that is 1-benzofuran substituted by a hydroxy group at position 6 and a 2-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-3,5-dihydroxyphenyl group at position 2.

cumic acid

4-09-00-01843 (Beilstein Handbook Reference)

C10H12O2 (164.0837)

4-Isopropylbenzoic acid, an aromatic monoterpenoid, is isolated from the stem bark of Bridelia retusa. 4-Isopropylbenzoic acid exhibits antifungal activities. 4-Isopropylbenzoic acid is also a reversible and uncompetitive inhibitor of mushroom tyrosinase[1][2]. 4-Isopropylbenzoic acid, an aromatic monoterpenoid, is isolated from the stem bark of Bridelia retusa. 4-Isopropylbenzoic acid exhibits antifungal activities. 4-Isopropylbenzoic acid is also a reversible and uncompetitive inhibitor of mushroom tyrosinase[1][2].

Barrelin

Naphtho(1,2-b)furan-2,6(3H,4H)-dione, 3a,5,5a,9,9a,9b-hexahydro-9-hydroxy-3,5a,9-trimethyl-, (3S-(3alpha,3aalpha,5abeta,9alpha,9aalpha,9bbeta))-

C15H20O4 (264.1362)

Durol

InChI=1\C10H14\c1-7-5-9(3)10(4)6-8(7)2\h5-6H,1-4H

C10H14 (134.1095)

586-81-2

Cyclohexanol, 1-methyl-4-(1-methylethylidene)-

C10H18O (154.1358)

D-DCTA

Butanedioic acid, 2,3-bis(((2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl)oxy)-, (2S,3S)-

C22H18O12 (474.0798)

505-56-6

1,20-Eicosanedicarboxylic acid

C22H42O4 (370.3083)

Resivit

rel-(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,4,5,7-tetrol

C15H14O7 (306.0739)

Leucocyanidin is an active anti-ulcerogenic ingredient was extracted from Litchi Chinensis. Leucocyanidin demonstrates a significant protective effect against Aspirin-induced erosions in rat models[1]. Leucocyanidin is an active anti-ulcerogenic ingredient was extracted from Litchi Chinensis. Leucocyanidin demonstrates a significant protective effect against Aspirin-induced erosions in rat models[1].

Ophiobolin F

C25H42O (358.3235)

N-Acetyl-ala-ala-ala-methylester

C12H21N3O5 (287.1481)

Ferric cyanide

C3FeN3 (133.9442)

N-(17-hydroxylinolenoyl)-L-glutamine

C23H38N2O5 (422.2781)

(7R,8Z)-bacteriochlorophyll b

C55H72MgN4O6 (908.5302)

Digalacturonic acid

4-O-alpha-D-Galactopyranuronosyl-D-galacturonic acid

C12H18O13 (370.0747)

Glycoside F

.BETA.-D-GLUCOPYRANOSIDE, (3.BETA.,25R)-26-(.BETA.-D-GLUCOPYRANOSYLOXY)-22-HYDROXYFUROST-5-EN-3-YL O-6-DEOXY-.ALPHA.-L-MANNOPYRANOSYL-(1->2)-O-(.BETA.-D-GLUCOPYRANOSYL-(1->4))-

C51H84O23 (1064.5403)

Deltoside is a steroid saponin. Protodeltonin is a natural product found in Balanites roxburghii, Trigonella foenum-graecum, and Balanites aegyptiaca with data available.

Docosanedioic_acid

1,20-Eicosanedicarboxylic acid

C22H42O4 (370.3083)

Docosanedioic acid is an alpha,omega-dicarboxylic acid that is docosane in which the methyl groups have been oxidised to the corresponding carboxylic acids. It has a role as a metabolite. It is an alpha,omega-dicarboxylic acid and a dicarboxylic fatty acid. It is a conjugate acid of a docosanedioate(2-). It derives from a hydride of a docosane. Docosanedioic acid is a natural product found in Pinus radiata with data available. An alpha,omega-dicarboxylic acid that is docosane in which the methyl groups have been oxidised to the corresponding carboxylic acids.

3-Methyl-2-butenal

C5H8O (84.0575)

triclofos

C2H4Cl3O4P (227.8913)

N - Nervous system > N05 - Psycholeptics > N05C - Hypnotics and sedatives C78272 - Agent Affecting Nervous System > C29756 - Sedative and Hypnotic

BENSULIDE

C14H24NO4PS3 (397.0605)

(S)-2-Propylpiperidine

C8H17N (127.1361)

phthalylsulfathiazole

C17H13N3O5S2 (403.0297)

Propoxycaine

C16H26N2O3 (294.1943)

mecoprop-p

C10H11ClO3 (214.0397)

16-Hentriacontanone

hentriacontan-16-one

C31H62O (450.48)

A dialkyl ketone that is hentriacontane in which the hydrogens at position 16 are replaced by an oxo group.

2-Oxohexanoic acid

C6H10O3 (130.063)

A straight-chain fatty acid consisting of hexanoic acid having an oxo group at position 2.

2-HYDROXYCYCLOHEXANONE

2-hydroxycyclohexanone dimer

C6H10O2 (114.0681)

alpha-Fenchol

(-)-alpha-fenchol

C10H18O (154.1358)

A fenchane monoterpenoid that is bicyclo[2.2.1]heptane substituted by methyl groups at positions 1, 3 and 3 and a hydroxy group at position 2 (the 1S,2S,4R stereoisomer).

2-Butynedioic acid

Acetylenedicarboxylic acid

C4H2O4 (113.9953)

gamma-Terpineol

C10H18O (154.1358)

2-(4-hydroxyphenyl)propanoic acid

C9H10O3 (166.063)

Coproporphyrinogen I

C36H44N4O8 (660.3159)

2-acetyllactic acid

2-hydroxy-2-methyl-3-oxobutanoic acid

C5H8O4 (132.0423)

A derivative of butyric acid having methyl, hydroxy and oxo substituents at the 2-, 2- and 3-positions respectively.

2-Methylbenzyl cyanide

2-(o-Tolyl)acetonitrile

C9H9N (131.0735)

5-Hydroxyvaleric Acid

5-HYDROXYPENTANOIC ACID

C5H10O3 (118.063)

An omega-hydroxy fatty acid consisting of pentanoic acid carrying a hydroxy group at C-5.

butirosin A

C21H41N5O12 (555.2752)

A butirosin that consists of neamine in which is substituted at position 2 by a beta-D-xylofuranosyl and at position 4 by an (S)-2-hydroxy-4-aminobutyryl group. D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents

3,6-Dichlorocatechol

C6H4Cl2O2 (177.9588)

2,3-Dihydroxyindole

C8H7NO2 (149.0477)

Uridine 2-phosphate

C9H13N2O9P (324.0359)

2-Deoxyinosine 5-monophosphate

C10H13N4O7P (332.0522)

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1-sulfinylpropane

Propanethial S-oxide, (1Z)-

C3H6OS (90.0139)

3-methylbut-2-enoyl-CoA

C26H42N7O17P3S (849.1571)

An unsaturated fatty acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of 3-methylbut-2-enoic acid.

(2E,6E)-2,6-dimethylocta-2,6-dienedial

C10H14O2 (166.0994)

8Z,11Z,14Z-eicosatrienoyl-CoA

all-cis-icosa-8,11,14-trienoyl-CoA

C41H68N7O17P3S (1055.3605)

An unsaturated fatty acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of all-cis-icosa-8,11,14-trienoic acid.

Isoglutamic acid

3-Aminopentanedioic acid

C5H9NO4 (147.0532)

A 1,5-dicarboxylic acid compound having a 3-amino substituent. It has been isolated from the extracts of the algae, Chondria armata.

Diacetazotol

C18H19N3O2 (309.1477)

hygrine

C8H15NO (141.1154)

A 1-(1-methylpyrrolidin-2-yl)acetone that has R configuration. It is a pyrrolidine alkaloid found in the coca plant, Erythroxylum coca.

2-amino-3-oxobutanoic acid

C4H7NO3 (117.0426)

An alpha-amino acid that is acetoacetic acid which is substituted by an amino group at position 2.

Allophanic acid

C2H4N2O3 (104.0222)

Aurasperone D

C31H24O10 (556.1369)

L-Lactaldehyde

C3H6O2 (74.0368)

10-Formyldihydrofolate

C20H21N7O7 (471.1502)

gamma-Glutamyl phosphate

C5H10NO7P (227.0195)

6-Lactoyltetrahydropterin

6-Lactoyl-5,6,7,8-tetrahydropterin

C9H13N5O3 (239.1018)

threo-3-methyl-L-aspartic acid

C5H9NO4 (147.0532)

An aspartic acid derivative having a 3-methyl substituent.

2,3,5-Trichlorobenzene-1,4-diol

C6H3Cl3O2 (211.9199)

(S)-Ureidoglycolate

C3H6N2O4 (134.0328)

(-)-7-Epi-alpha-selinene

C15H24 (204.1878)

An isomer of selinene where the double bond in the octahydronaphthalene ring system is endocyclic with (2S,4aR,8aR)-configuration.

2-Hexaprenyl-3-methyl-6-methoxy-1,4 benzoquinone

C38H56O3 (560.4229)

(R)-2-Methylpyrrolidine

(R)-2-Methyl-pyrrolidine

C5H11N (85.0891)

A 2-methylpyrrolidine that has (R)-configuration.

3-Ketovaleric acid

3-Oxopentanoic acid

C5H8O3 (116.0473)

1-Deoxy-D-xylulose

C5H10O4 (134.0579)

alpha-Ribazole

C14H18N2O4 (278.1267)

but-3-ynal

C4H4O (68.0262)

A butynal which has a monosubstituted triple bond.

(2S,3R)-3-hydroxybutane-1,2,3-tricarboxylic acid

C7H10O7 (206.0427)

A 3-hydroxybutane-1,2,3-tricarboxylic acid which has (2S,3R) configuration.

alpha-Cyclocostunolide

C15H20O2 (232.1463)

19-Oxotestosterone

C19H26O3 (302.1882)

2beta,3beta,5beta,14,20,22R,25-heptahydroxycholest-7-en-6-one

C27H44O8 (496.3036)

(R)-Norreticuline

C18H21NO4 (315.1471)

Raucaffricine

C27H32N2O8 (512.2159)

4-amino-2-methyl-5-phosphooxymethylpyrimidine

(4-AMINO-2-METHYLPYRIMIDIN-5-YL)METHYL DIHYDROGEN PHOSPHATE

C6H10N3O4P (219.0409)

An aminopyrimidine having the amino group at the 4-position together with methyl and phosphooxymethyl groups at the 2- and 5-positions respectively.

Cmp-2-keto-3-deoxy-octulosonic acid

C17H26N3O15P (543.1101)

phosphonoacetaldehyde

C2H5O4P (123.9925)

A phosphonic acid consisting of acetaldehyde with the phospho group at the 2-position.

Procyanidin B5

C30H26O12 (578.1424)

A proanthocyanidin consisting of two molecules of (-)-epicatechin joined by a bond between positions 4 and 6 in beta-configuration. It can be found in grape seeds, in Hibiscus cannabinus (kenaf) root and bark, in apple and in cacao.

Cifostodine

2,3-cyclic CMP

C9H12N3O7P (305.0413)

Sorgolactone

C18H20O5 (316.1311)

Thiourocanic acid

C6H6N2O2S (170.015)

(3S)-3,6-Diaminohexanoic acid

C6H14N2O2 (146.1055)

5-(5-(2,6-Dichloro-4-(4,5-Dihydro-2-Oxazoly)phenoxy)pentyl)-3-Methyl Isoxazole

C18H20Cl2N2O3 (382.0851)

(1E)-4-oxobut-1-ene-1,2,4-tricarboxylic acid

C7H6O7 (202.0114)

Allopregnan-20alpha-ol-3-one

C21H34O2 (318.2559)

2-Methylpropanal O-methyloxime

C5H11NO (101.0841)

Antibiotic JI-20A

C19H39N5O9 (481.2748)

D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D005839 - Gentamicins

UDP-4-dehydro-6-deoxy-D-glucose

C15H22N2O16P2 (548.0445)

2-(2-methylthioethyl)malic acid

C7H12O5S (208.0405)

3-Methyl-6-methoxy-2-octaprenyl-1,4-benzoquinone

C48H72O3 (696.5481)

N-Hydroxytyrosine

N-Hydroxy-L-tyrosine

C9H11NO4 (197.0688)

Deoxy-5-methylcytidylic acid

C10H16N3O7P (321.0726)

Fernenol

C30H50O (426.3861)

Cellobiono-1,5-lactone

C12H20O11 (340.1006)

Calystegin b2

C7H13NO4 (175.0845)

3-O-Acetylhamayne

C18H19NO5 (329.1263)

8(R)-HPETE

C20H32O4 (336.23)

The (R)-enantiomer of 8-HPETE.

N-(2,4-diamino-6-hydroxypyrimidin-5-yl)-N-methylformamide

C6H9N5O2 (183.0756)

2-Oxosuccinamic acid

C4H5NO4 (131.0219)

Clavaminic acid

C8H10N2O4 (198.0641)

Calystegin A3

C7H13NO3 (159.0895)

(+)-galbacin

C20H20O5 (340.1311)

Formimidoyl-fortimicin A

C18H36N6O6 (432.2696)

(E)-2-Butenyl-4-methyl-threonine

C9H17NO3 (187.1208)

N(6)-[(indol-3-yl)acetyl]-L-lysine

C16H21N3O3 (303.1583)

D006133 - Growth Substances > D010937 - Plant Growth Regulators > D007210 - Indoleacetic Acids

S-(5-Deoxy-D-ribos-5-yl)-L-homocysteine

C9H17NO6S (267.0777)

S-(PGA1)-glutathione

C30H49N3O10S (643.3138)

Sulfoacetate

SULFOACETIC ACID

C2H4O5S (139.9779)

A carboxyalkanesulfonic acid that is the C-sulfo derivative of acetic acid.

alpha1-Sitosterol

C30H50O (426.3861)

Fluoroacetaldehyde

C2H3FO (62.0168)

2-Methyl-1-(2,4,6-trihydroxyphenyl)butan-1-one

C11H14O4 (210.0892)

CoA 24:1

(15Z)-tetracosenoyl-coenzyme A;(Z)-15-tetracosenoyl-CoA;15cis-tetracosenoyl-CoA;15cis-tetracosenoyl-coenzyme A;Tetracosenoyl-CoA;nervonoyl-CoA;nervonoyl-coenzyme A

C45H80N7O17P3S (1115.4544)

A very long-chain fatty acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of (15Z)-tetracosenoic acid.

ent-7beta-Hydroxykaurenoic acid

ent-7alpha-Hydroxykaur-16-en-19-oic acid

C20H30O3 (318.2195)

Apiitol

C5H12O5 (152.0685)

2,2-Dichloroacetaldehyde

C2H2Cl2O (111.9483)

CYCLOHEXYL ACETATE

C8H14O2 (142.0994)

2-Ene-vpa

2-N-Propyl-2-pentenoic acid

C8H14O2 (142.0994)

D002491 - Central Nervous System Agents > D000927 - Anticonvulsants D009676 - Noxae > D013723 - Teratogens

DIDECYL PHTHALATE

Didecyl 1,2-benzenedicarboxylate

C28H46O4 (446.3396)

PCB 8

2,4-DICHLOROBIPHENYL

C12H8Cl2 (222.0003)

D004785 - Environmental Pollutants > D011078 - Polychlorinated Biphenyls

4-Butylphenol

p-Hydroxybutylbenzene

C10H14O (150.1045)

Durene

1,2,4,5-TETRAMETHYLBENZENE

C10H14 (134.1095)

PCB 155

2,2,4,4,6,6-HEXACHLOROBIPHENYL

C12H4Cl6 (357.8444)

D004785 - Environmental Pollutants > D011078 - Polychlorinated Biphenyls

PCB 21

2,3,4-Trichlorobiphenyl

C12H7Cl3 (255.9613)

(R)-2-(8,8-dimethyl-2,3,4,8-tetrahydropyrano[2,3-f]chromen-3-yl)-5-methoxyphenol

C21H22O4 (338.1518)

Kaur-16-ene

C20H32 (272.2504)

1-Aminoethylphosphonic acid

DL-1-(Aminoethyl)phosphonic acid

C2H8NO3P (125.0242)

6-Thiourate

6-Thiouric acid

C5H4N4O2S (184.0055)

Furofoline I

C16H11NO3 (265.0739)

6alpha-Hydroxymaackiain

C16H12O6 (300.0634)

(-)-Chimonanthine

C22H26N4 (346.2157)

Alcophosphamide

C7H17Cl2N2O3P (278.0354)

D000970 - Antineoplastic Agents > D018906 - Antineoplastic Agents, Alkylating > D009588 - Nitrogen Mustard Compounds D000970 - Antineoplastic Agents > D018906 - Antineoplastic Agents, Alkylating > D010752 - Phosphoramide Mustards

2-Amino-6-(1,2-dihydroxypropyl)-4a-hydroxy-1,5,6,7-tetrahydropteridin-4-one

C9H15N5O4 (257.1124)

3,5,14-trihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carboxaldehyde

C23H32O6 (404.2199)