Exact Mass: 467.95050960000003
Exact Mass Matches: 467.95050960000003
Found 37 metabolites which its exact mass value is equals to given mass value 467.95050960000003,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Deoxyuridine triphosphate
Dutp, also known as 2-deoxyuridine 5-triphosphate or deoxy-utp, is a member of the class of compounds known as pyrimidine 2-deoxyribonucleoside triphosphates. Pyrimidine 2-deoxyribonucleoside triphosphates are pyrimidine nucleotides with a triphosphate group linked to the ribose moiety lacking a hydroxyl group at position 2. Dutp is slightly soluble (in water) and an extremely strong acidic compound (based on its pKa). Dutp can be found in a number of food items such as bilberry, japanese chestnut, black radish, and lovage, which makes dutp a potential biomarker for the consumption of these food products. Dutp can be found primarily in prostate Tissue, as well as throughout most human tissues. Dutp exists in all living species, ranging from bacteria to humans. In humans, dutp is involved in the pyrimidine metabolism. Dutp is also involved in few metabolic disorders, which include beta ureidopropionase deficiency, dihydropyrimidinase deficiency, MNGIE (mitochondrial neurogastrointestinal encephalopathy), and UMP synthase deficiency (orotic aciduria). Moreover, dutp is found to be associated with prostate cancer. Dutp is a non-carcinogenic (not listed by IARC) potentially toxic compound. Metabolism of organophosphates occurs principally by oxidation, by hydrolysis via esterases and by reaction with glutathione. Demethylation and glucuronidation may also occur. Oxidation of organophosphorus pesticides may result in moderately toxic products. In general, phosphorothioates are not directly toxic but require oxidative metabolism to the proximal toxin. The glutathione transferase reactions produce products that are, in most cases, of low toxicity. Paraoxonase (PON1) is a key enzyme in the metabolism of organophosphates. PON1 can inactivate some organophosphates through hydrolysis. PON1 hydrolyzes the active metabolites in several organophosphates insecticides as well as, nerve agents such as soman, sarin, and VX. The presence of PON1 polymorphisms causes there to be different enzyme levels and catalytic efficiency of this esterase, which in turn suggests that different individuals may be more susceptible to the toxic effect of organophosphate exposure (T3DB). Deoxyuridine triphosphate (dUTP) is a deoxynucleotide triphosphate (dNTP) that is chemically similar to uridine triphosphate (UTP) except that it has a deoxyribose sugar instead of a ribose sugar. DNA synthesis requires the availability of deoxynucleotide triphosphates (dTTP, dATP, dGTP, dCTP), whereas RNA synthesis requires the availability of nucleotide triphosphates (NTPs) such as TTP, ATP, GTP, and UTP. The conversion of nucleotide triphosphates (NTPs) into dNTPs can only be done in the diphosphate form. Typically, an NTP has one phosphate removed to become an NDP. This is then converted into a dNDP by an enzyme called ribonucleotide reductase and followed by the re-addition of phosphate to give a dNTP. dUTP is a substrate for several enzymes, including inosine triphosphate pyrophosphatase, deoxyuridine 5-triphosphate nucleotidohydrolase (mitochondrial), uridine-cytidine kinase 1, nucleoside diphosphate kinase 3, nucleoside diphosphate kinase B, nucleoside diphosphate kinase 6, nucleoside diphosphate kinase (mitochondrial), nucleoside diphosphate kinase homolog 5, nucleoside diphosphate kinase A, and nucleoside diphosphate kinase 7. While UTP is routinely incorporated into RNA, dUTP is not normally incorporated into DNA. Instead, if dUTP is misincorporated into DNA, it can cause DNA damage. Therefore, dUTP can be considered as a teratogen or a mutagen. The extent of DNA damage caused by dUTP is highly dependent on the levels of the dUTP pyrophosphatase (dUTPase) and uracil-DNA glycosylase (UDG), which limits the intracellular accumulation of dUTP. Additionally, loss of viability following thymidylate synthase (TS) inhibition occurs as a consequence of the accumulation of dUTP in some cell lines and subsequent misincorporation of uracil into DNA (PMID: 11487279).
alpha-D-Ribose 1-methylphosphonate 5-triphosphate
C6H16O16P4 (467.93888560000005)
2-[3-(4-Chlorophenyl)-2-[(2,4-dichlorobenzoyl)imino]-4-oxo-5-thiazolidinylidene]-acetic acid, methyl ester
C19H11Cl3N2O4S (467.95050960000003)
Indigotin disulfonate sodium
Colour additive for food
4-(3-Chloro-2-cyanophenoxy)-N-(3,5-dichloro-4-pyridinyl)benzenesulfonohydrazide
5-acetoxy-2,10-dibromo-3-chloro-7alpha,8alpha-epoxy-alpha-chamigrene
C17H23Br2ClO3 (467.97023580000007)
4, 19-Dibromo-3-ethyl-2, 20-dioxabicyclo[14.3.1]eicosa-1(19), 6, 9, 16-tetraen-12-yn-18-one, 9CI
C20H22Br2O3 (467.99355819999994)
Dibrompropamidine
C17H18Br2N4O2 (467.97964079999997)
D - Dermatologicals > D08 - Antiseptics and disinfectants > D08A - Antiseptics and disinfectants > D08AC - Biguanides and amidines S - Sensory organs > S01 - Ophthalmologicals > S01A - Antiinfectives C254 - Anti-Infective Agent > C28394 - Topical Anti-Infective Agent D000890 - Anti-Infective Agents
2-Deoxythymidine-5-diphosphate trisodium salt
C10H13N2Na3O11P2 (467.96876879999996)
5-bromo-1,3-bis(bromomethyl)-2-octoxybenzene
C16H23Br3O (467.92988879999996)
2-[4-bromo-2-[1-(2,6-dichlorophenyl)pyrazole-4-carbonyl]phenoxy]acetic acid
Clobenpropit dihydrobromide
C14H19Br2ClN4S (467.93856040000003)
Clobenpropit dihydrobromide is a potent histamine H3R antagonist/inverse agonist with a pEC50 of 8.07 for histamine H3LR[1]. Clobenpropit dihydrobromide acts as partial agonist at histamine H4 receptors (Ki 13 nM). Clobenpropit dihydrobromide also binds to serotonin 5-HT3 receptors (Ki 7.4 nM) and α2A/α2C adrenoceptors (Ki 17.4/7.8 nM)[2]. Clobenpropit dihydrobromide increases apoptosis[3].
2,3,4,5-tetrachloro-6-(3-hydroxy-6-oxoxanthen-9-yl)benzoic acid
C20H8Cl4O5 (467.91258380000005)
N-CYANO-3-(IODOMETHYL)-4-(1H,1H-NONAFLUOROPENTYL)PYRROLIDINE
2-[3-(4-Chlorophenyl)-2-[(2,4-dichlorobenzoyl)imino]-4-oxo-5-thiazolidinylidene]-acetic acid, methyl ester
C19H11Cl3N2O4S (467.95050960000003)
4-tert-butyl-N-[(1E)-(3,5-dibromo-2,4-dihydroxyphenyl)methylidene]benzohydrazide
7-Bromo-2-{(E)-1-[5-(2-nitrophenyl)-2-furyl]methylidene}[1,3]thiazolo[2,3:2,3]imidazo[4,5-B]pyridin-3(2H)-one
C19H9BrN4O4S (467.95278540000004)
(2r,3s,5r,6s,8r)-3,6-dibromo-8-[(3z)-1-chlorohex-3-en-5-yn-1-yl]-2-ethyloxocan-5-yl acetate
C17H23Br2ClO3 (467.97023580000007)
3-[(2,3-dibromo-4,5-dihydroxyphenyl)methyl]-3a,6-dihydroxy-3-methoxy-dihydro-5h-furo[3,2-b]furan-2-one
methyl 3',4-dibromo-4'-chloro-1,3,3,4'-tetramethyl-7-oxaspiro[bicyclo[4.1.0]heptane-2,1'-cyclohexan]-4-ene-6'-carboxylate
C17H23Br2ClO3 (467.97023580000007)
methyl (1s,2s,3's,4's,6r,6's)-3',4-dibromo-4'-chloro-1,3,3,4'-tetramethyl-7-oxaspiro[bicyclo[4.1.0]heptane-2,1'-cyclohexan]-4-ene-6'-carboxylate
C17H23Br2ClO3 (467.97023580000007)
4,19-dibromo-3-ethyl-2,20-dioxabicyclo[14.3.1]icosa-1(19),6,9,16-tetraen-12-yn-18-one
C20H22Br2O3 (467.99355819999994)
(3s,4r,6e,9z)-4,19-dibromo-3-ethyl-2,20-dioxabicyclo[14.3.1]icosa-1(19),6,9,16-tetraen-12-yn-18-one
C20H22Br2O3 (467.99355819999994)