Exact Mass: 516.3271314
Exact Mass Matches: 516.3271314
Found 500 metabolites which its exact mass value is equals to given mass value 516.3271314
,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Fusidic Acid
Fusidic acid is a steroid antibiotic that is isolated from the fermentation broth of Fusidium coccineum. It has a role as a protein synthesis inhibitor, an EC 2.7.1.33 (pantothenate kinase) inhibitor and an Escherichia coli metabolite. It is a 3alpha-hydroxy steroid, an 11alpha-hydroxy steroid, a sterol ester, a steroid acid, an alpha,beta-unsaturated monocarboxylic acid and a steroid antibiotic. It is a conjugate acid of a fusidate. It derives from a hydride of a 5alpha-cholestane. An antibiotic isolated from the fermentation broth of Fusidium coccineum. (From Merck Index, 11th ed) It acts by inhibiting translocation during protein synthesis. It is often used topically in creams and eyedrops but is available in systemic formulations including tablets and injections. Fusidic acid is a natural product found in Epidermophyton floccosum, Stilbella aciculosa, and other organisms with data available. Fusidic Acid is a bacteriostatic antibiotic derived from the fungus Fusidium coccineum and used as a topical medication to treat skin infections. Fusidic acid acts as a bacterial protein synthesis inhibitor by preventing the turnover of elongation factor G (EF-G) from the ribosome. Fusidic acid is effective primarily on gram-positive bacteria. An antibiotic isolated from the fermentation broth of Fusidium coccineum. (From Merck Index, 11th ed). It acts by inhibiting translocation during protein synthesis. See also: Fusidate Sodium (active moiety of). Fusidic Acid is only found in individuals that have used or taken this drug. It is an antibiotic isolated from the fermentation broth of Fusidium coccineum. (From Merck Index, 11th ed) It acts by inhibiting translocation during protein synthesis.Fusidic acid works by interfering with bacterial protein synthesis, specifically by preventing the translocation of the elongation factor G (EF-G) from the ribosome. It also can inhibit chloramphenicol acetyltransferase enzymes. J - Antiinfectives for systemic use > J01 - Antibacterials for systemic use > J01X - Other antibacterials > J01XC - Steroid antibacterials D - Dermatologicals > D09 - Medicated dressings > D09A - Medicated dressings > D09AA - Medicated dressings with antiinfectives D - Dermatologicals > D06 - Antibiotics and chemotherapeutics for dermatological use > D06A - Antibiotics for topical use S - Sensory organs > S01 - Ophthalmologicals > S01A - Antiinfectives > S01AA - Antibiotics A steroid antibiotic that is isolated from the fermentation broth of Fusidium coccineum. D004791 - Enzyme Inhibitors > D011500 - Protein Synthesis Inhibitors C254 - Anti-Infective Agent > C28394 - Topical Anti-Infective Agent D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents C254 - Anti-Infective Agent > C52588 - Antibacterial Agent COVID info from PDB, Protein Data Bank C784 - Protein Synthesis Inhibitor Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Fusidic acid (Fusidate) a bacteriostatic antibiotic produced from the Fusidium coccineum fungus, belongs to the class of steroids. Fusidic acid has no corticosteroid effects. Fusidic acid inhibits the growth of bacteria by preventing the release of translation elongation factor G (EF-G) from the ribosome[1][2].
Cucurbitacin D
Cucurbitacin D is a cucurbitacin in which a lanostane skeleton is multi-substituted with hydroxy, methyl and oxo substituents, with unsaturation at positions 5 and 23. It is a cucurbitacin, a secondary alpha-hydroxy ketone and a tertiary alpha-hydroxy ketone. It derives from a hydride of a lanostane. Cucurbitacin D is a natural product found in Elaeocarpus chinensis, Elaeocarpus hainanensis, and other organisms with data available. Cucurbitacin D is found in calabash. Cucurbitacin D is isolated from plants of the Cucurbitacea Cucurbitacin D is an active component in Trichosanthes kirilowii, disrupts interactions between Hsp90 and two co-chaperones, Cdc37 and p23. Cucurbitacin D prevents Hsp90 client (Her2, Raf, Cdk6, pAkt) maturation without induction of the heat shock response. Anti-cancer activity[1]. Cucurbitacin D is an active component in Trichosanthes kirilowii, disrupts interactions between Hsp90 and two co-chaperones, Cdc37 and p23. Cucurbitacin D prevents Hsp90 client (Her2, Raf, Cdk6, pAkt) maturation without induction of the heat shock response. Anti-cancer activity[1].
Probucol
Probucol is only found in individuals that have used or taken this drug. It is a drug used to lower LDL and HDL cholesterol yet has little effect on serum-triglyceride or VLDL cholesterol. (From Martindale, The Extra Pharmacopoeia, 30th ed, p993).Probucol lowers serum cholesterol by increasing the fractional rate of low-density lipoprotein (LDL) catabolism in the final metabolic pathway for cholesterol elimination from the body. Additionally, probucol may inhibit early stages of cholesterol biosynthesis and slightly inhibit dietary cholesterol absorption. Recent information suggests that probucol may inhibit the oxidation and tissue deposition of LDL cholesterol, thereby inhibiting atherogenesis. It appears to inhibits ABCA1-mediated cellular lipid efflux. D057847 - Lipid Regulating Agents > D000960 - Hypolipidemic Agents > D000924 - Anticholesteremic Agents C - Cardiovascular system > C10 - Lipid modifying agents > C10A - Lipid modifying agents, plain C78276 - Agent Affecting Digestive System or Metabolism > C29703 - Antilipidemic Agent D020011 - Protective Agents > D000975 - Antioxidants D009676 - Noxae > D000963 - Antimetabolites
Adynerin
Adynerin is a natural steroid found in the herbs of Nerium oleander.
L-Olivosyl-oleandolide
3-O-(alpha-L-olivosyl)oleandolide is a macrolide that is oleandolide having a 2,6-dideoxy-alpha-L-arabino-hexopyranosyl (alpha-L-olivosyl) residue attached at position 3. It has a role as a metabolite. It is a macrolide, a glycoside and a monosaccharide derivative. It is functionally related to an oleandolide. L-Olivosyl-oleandolide is a naturally occurring sesquiterpene lactone derivative that contains an olivosyl moiety, which is a specific type of ester derived from olivolic acid. The "L" in the name indicates that the olivosyl group is in the L-configuration, which refers to the spatial arrangement of atoms around the chiral center in the molecule. This compound is an example of a glycosylated sesquiterpene lactone, where the sesquiterpene lactone oleandolide is modified by the attachment of the olivosyl group. The presence of the olivosyl group can alter the biological properties of the parent compound, oleandolide, potentially affecting its pharmacological activities such as cytotoxicity, anti-inflammatory effects, and antimicrobial activity. L-Olivosyl-oleandolide can be found in certain plant species and may contribute to the plant's defense mechanisms against pathogens and herbivores. In its chemical structure, L-Olivosyl-oleandolide consists of a sesquiterpene lactone core with a lactone ring fused to a sesquiterpene framework, and it is appended with the L-olivosyl ester group, which adds complexity to its molecular structure and function. This compound is of interest in the fields of natural products chemistry and pharmacognosy for its potential therapeutic applications and as a subject of study for understanding the biosynthesis of such natural products.
Ganoderenic acid C
Ganoderenic acid C is found in mushrooms. Ganoderenic acid C is a constituent of fungus Ganoderma lucidum (reishi) Constituent of fungus Ganoderma lucidum (reishi). Ganoderenic acid C is found in mushrooms.
Ganoderic acid A
Ganoderic acid A is found in mushrooms. Ganoderic acid A is a constituent of Ganoderma lucidum (reishi) Constituent of Ganoderma lucidum (reishi). Ganoderic acid A is found in mushrooms. Ganoderic acid A can inhibit of the JAK-STAT3 signaling pathway, also inhibit proliferation, viability, ROS. Ganoderic acid A can inhibit of the JAK-STAT3 signaling pathway, also inhibit proliferation, viability, ROS.
Ganoderic acid B
Ganoderic acid B is found in mushrooms. Ganoderic acid B is a constituent of Ganoderma lucidum (reishi) Constituent of Ganoderma lucidum (reishi). Ganoderic acid B is found in mushrooms. Ganoderic acid B is a triterpene isolated from a mushroom Ganoderma lucidum. Ganoderic acid B inhibits the activation of Epstein-Barr virus (EBV) antigens as telomerase inhibitor. Ganoderic acid B is a moderately active inhibitor against HIV-1 protease[1][2][3]. Ganoderic acid B is a triterpene isolated from a mushroom Ganoderma lucidum. Ganoderic acid B inhibits the activation of Epstein-Barr virus (EBV) antigens as telomerase inhibitor. Ganoderic acid B is a moderately active inhibitor against HIV-1 protease[1][2][3].
Ganoderic acid epsilon
Ganoderic acid epsilon is found in mushrooms. Ganoderic acid epsilon is a constituent of Ganoderma lucidum (reishi) Constituent of Ganoderma lucidum (reishi). Ganoderic acid epsilon is found in mushrooms.
Phytolaccinic acid
Aglycone from the berries of Phytolacca americana (pokeberry). Phytolaccinic acid is found in fruits. Phytolaccinic acid is found in fruits. Aglycone from the berries of Phytolacca americana (pokeberry
Ganoderic acid delta
Ganoderic acid gamma is found in mushrooms. Ganoderic acid gamma is a constituent of Ganoderma lucidum (reishi) Constituent of Ganoderma lucidum (reishi). Ganoderic acid delta is found in mushrooms.
Pokeberrygenin
Pokeberrygenin is found in fruits. Pokeberrygenin is isolated from Phytolacca americana berries (pokeberry Isolated from Phytolacca americana berries (pokeberry). Pokeberrygenin is found in fruits.
(Z)-2-((3R,4S,8S,9S,10S,11R,13R,14S,16S)-16-Acetoxy-3,11-dihydroxy-4,8,10,14-tetramethyldodecahydro-1H-cyclopenta[a]phenanthren-17(2H,10H,14H)-ylidene)-6-methylhept-5-enoic acid
Oleaside A
Ganoderenic acid c
Ganoderenic acid C is a triterpenoid.
Ganoderic acid B
Ganoderic acid B is a triterpenoid. Ganoderic acid B is a natural product found in Ganoderma sinense and Ganoderma lucidum with data available. See also: Reishi (part of). Ganoderic acid B is a triterpene isolated from a mushroom Ganoderma lucidum. Ganoderic acid B inhibits the activation of Epstein-Barr virus (EBV) antigens as telomerase inhibitor. Ganoderic acid B is a moderately active inhibitor against HIV-1 protease[1][2][3]. Ganoderic acid B is a triterpene isolated from a mushroom Ganoderma lucidum. Ganoderic acid B inhibits the activation of Epstein-Barr virus (EBV) antigens as telomerase inhibitor. Ganoderic acid B is a moderately active inhibitor against HIV-1 protease[1][2][3].
3-Ac 鈥樎?3alpha,5alpha,11beta,20R,22xi,24xi)-22,25-Epoxy-3,11-dihydroxy-24-methylfurostano-18,20-lactone
(22S)-2alpha-hydroxy-3alpha-acetoxy-24-methyl-11beta,18;18,20beta;22,25-triepoxy-5alpha-furostane
(4Z)-1-(8-acetoxyocatadec-4-enoyl)-2,6-diacetoxybenzene
6-O-Acetyl-2,3,4-tri-O-<(+)-3-methylvaleryl>-beta-D-glucose
Di-Ac-(3alpha,5alpha,23S,25R)-Spirostane-3,23-diol
(1beta,5beta,7alpha,8xi,9beta,10alpha,11alpha,14beta)-7,8,11,14-tetrahydroxypimar-15-en-1-yl beta-D-glucopyranoside|ent-isopimanervoside B
3beta,6alpha-Diacetoxy-20xi-hydroxy-5alpha-cholest-9(11)-en-23-on|3beta,6alpha-diacetoxy-20xi-hydroxy-5alpha-cholest-9(11)-en-23-one|Diacetyl-thornasterosol A
14-hydroxy-3beta-(O3-methyl-alpha-L-arabino-2,6-dideoxy-hexopyranosyloxy)-5beta,14beta-carda-16,20(22)-dienolide|14-Hydroxy-3beta-(O3-methyl-alpha-L-arabino-2,6-didesoxy-hexopyranosyloxy)-5beta,14beta-carda-16,20(22)-dienolid
Isocucurbitacin D
16beta,22-diacetoxy-24-methyl-12,24-dioxoscalaran-25-al
lycernuic ketone B|methyl 3alpha,21beta,29-trihydroxy-16-oxoserrat-14-en-24-carboxylate
5alpha-cholestane-3beta,4beta,5,6alpha,8,14,15alpha,24,26-nonaol
2,3-seco-taraxer-14-ene-2,3,28-trioic acid 3-methyl ester
Di-Ac-(1beta,3beta,5alpha,25R)-Spirostane-1,3-diol
2,6-Diacetyl-3,4-diisobutyryl-1-O-octylglucopyranoside
(3beta)-3,29-dihydroxy-23-methoxy-23-oxoolean-12-en-28-oic acid|kalidiumin
IC202C
An aldoxime isolated from Streptoalloteichus sp.1454-19. It is a siderophore which exhibits immunosuppressive activity on a mixed lymphocyte culture reaction (MLCR).
rel-18(S),19(R)-diacetoxy-18,19-epoxy-2(R)-hexanyloxy-5(R),8(S),9(S),10(R)-cleroda-3,13(16),14-triene
25-hydroxy-6-oxocholest-4-en-3alpha,11alpha-diyl diacetate
1-O-acetyl-2-O-[(3R,7R)-3,7-bis(acetyloxy)octadecanoyl]-sn-glycerol
12alpha,16beta-diacetoxy-20,24-dimethyl-24-oxoscalar-25-al|12alpha,16beta-diacetoxy-20,24-dimethyl-24-oxoscalaran-25-al
(22S)-2alpha-acetoxy-3alpha-hydroxy-24-methyl-11beta,18;18,20beta;22,25-triepoxy-5alpha-furostane
3beta,7beta,15beta-trihydroxy-11,23-dioxo-lanost-8,16-dien-26-oic acid
1-O-linoloyl-3-O-beta-D-galactopyranosyl-sn-glycerol
2beta,15S,16,17,19-pentahydroxyisopimar-8(14)-ene 17-O-beta-D-glucopyranoside
13,27-cyclo-3alpha,16alpha,29-trihydroxyolean-11-ene-24,28-dioic acid|donellanic acid C
(1R)-1,4-epoxy-11alpha-hydroxy-3,4-seco-lup-20(30)-ene-3,28-dioic acid 3-methyl ester|acanthosessiligenin II
(24E)-3alpha-9alpha-23alpha-trihydroxy-15-oxo-17,14-friedolanosta-8(14),24-dien-26-oate|garcihombronane L
1,3,7-Tris(3-methyl-2-butenyl)-4-methoxy-5-benzoyl-8,8-dimethylbicyclo[3.3.1]non-3-ene-2,9-dione
Methyl (24E)-3??,23??-dihydroxy-8??,9??-epoxy-15-oxo-17,14-friedo-lanostan-24-en-26-oate
caseargrewiin H|rel-(2R,5S,8R,9R,10S,18R,19S)-18,19-diacetoxy-18,19-epoxy-2-hexanoyloxycleroda-3,12(Z),14-triene
21-O-alpha-L-rhamnopyranosyl-18R-hydroxydihydroalloprotolichesterinate
(20xi)-16alpha,25-dihydroxy-3,4-seco-24-methyllanosta-4(28),8,24(241)-triene-3,21-dioic acid|25-hydroxyporicoic acid H
(20R,22R)-3beta-acetoxy-1alpha,12beta,20-trihydroxy-witha-5,24-dienolide
21R,23R-epoxy-7alpha,24S-dihydroxy-21alpha,25-dimethoxyapotirucalla-1,14-dien-3-one|holstinone A
3beta,22alpha-dihydroxy-23-oxo-12-oleanene-28,29-dioic acid
methyl 3-oxo-1alpha,19alpha,28-trihydroxyurs-12-en-24-oate
2beta.3beta-Dihydroxy-27-nor-oleanen-(13)-disaeure-(23.28)-28-aethylester|2beta.3beta-dihydroxy-27-nor-oleanene-(13)-dioic acid-(23.28)-28-ethyl ester|Senegensaeuremonoethylester
Ile Gln Lys Glu
Lys Gln Ile Glu
Ganoderic_acid
Ganoderic acid A is a triterpenoid. Ganoderic acid A is a natural product found in Ganoderma sinense, Ganoderma lucidum, and Wolfiporia cocos with data available. See also: Reishi (part of). Ganoderic acid A can inhibit of the JAK-STAT3 signaling pathway, also inhibit proliferation, viability, ROS. Ganoderic acid A can inhibit of the JAK-STAT3 signaling pathway, also inhibit proliferation, viability, ROS.
Ganoderic acid ε
Ganoderic acid epsilon is a triterpenoid. Ganoderic acid epsilon is a natural product found in Ganoderma lucidum with data available.
Phytolaccagenic acid
Phytolaccagenic acid is a natural product found in Anisomeria coriacea, Diploclisia glaucescens, and other organisms with data available.
Cucurbitacin D
Glycoside from leaves and fruit of Cucumis sativus (cucumber). Cucurbitacide E is found in cucumber and green vegetables. Cucurbitacin D is an active component in Trichosanthes kirilowii, disrupts interactions between Hsp90 and two co-chaperones, Cdc37 and p23. Cucurbitacin D prevents Hsp90 client (Her2, Raf, Cdk6, pAkt) maturation without induction of the heat shock response. Anti-cancer activity[1]. Cucurbitacin D is an active component in Trichosanthes kirilowii, disrupts interactions between Hsp90 and two co-chaperones, Cdc37 and p23. Cucurbitacin D prevents Hsp90 client (Her2, Raf, Cdk6, pAkt) maturation without induction of the heat shock response. Anti-cancer activity[1].
9-hydroxy-5b,8,11a-trimethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a,5a,8-tricarboxylic acid
9-hydroxy-5b,8,11a-trimethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a,5a,8-tricarboxylic acid_32.4\\%
9-hydroxy-5b,8,11a-trimethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a,5a,8-tricarboxylic acid_major
(6R)-6-((3S,5S,9S,10S,13S,14S,17R)-3-acetoxy-10,13-dimethyl-7,16-dioxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methylheptyl acetate
Ala Ile Lys Trp
Ala Ile Trp Lys
Ala Lys Ile Trp
Ala Lys Leu Trp
Ala Lys Trp Ile
Ala Lys Trp Leu
Ala Leu Lys Trp
Ala Leu Trp Lys
Ala Trp Ile Lys
Ala Trp Lys Ile
Ala Trp Lys Leu
Ala Trp Leu Lys
Asp Lys Arg Val
C21H40N8O7 (516.3019810000001)
Asp Lys Val Arg
C21H40N8O7 (516.3019810000001)
Asp Arg Lys Val
C21H40N8O7 (516.3019810000001)
Asp Arg Val Lys
C21H40N8O7 (516.3019810000001)
Asp Val Lys Arg
C21H40N8O7 (516.3019810000001)
Asp Val Arg Lys
C21H40N8O7 (516.3019810000001)
Glu Ile Lys Lys
Glu Ile Lys Gln
Glu Lys Ile Lys
Glu Lys Lys Ile
Glu Lys Lys Leu
Glu Lys Leu Lys
Glu Leu Lys Lys
Ile Ala Lys Trp
Ile Ala Trp Lys
Ile Glu Lys Lys
Ile Lys Ala Trp
Ile Lys Glu Lys
Ile Lys Lys Glu
Ile Lys Arg Thr
Ile Lys Thr Arg
Ile Lys Trp Ala
Ile Gln Arg Thr
C21H40N8O7 (516.3019810000001)
Ile Gln Thr Arg
C21H40N8O7 (516.3019810000001)
Ile Arg Lys Thr
Ile Arg Gln Thr
C21H40N8O7 (516.3019810000001)
Ile Arg Thr Lys
Ile Arg Thr Gln
C21H40N8O7 (516.3019810000001)
Ile Thr Lys Arg
Ile Thr Gln Arg
C21H40N8O7 (516.3019810000001)
Ile Thr Arg Lys
Ile Thr Arg Gln
C21H40N8O7 (516.3019810000001)
Ile Trp Ala Lys
Ile Trp Lys Ala
Lys Ala Ile Trp
Lys Ala Leu Trp
Lys Ala Trp Ile
Lys Ala Trp Leu
Lys Asp Arg Val
C21H40N8O7 (516.3019810000001)
Lys Asp Val Arg
C21H40N8O7 (516.3019810000001)
Lys Glu Ile Lys
Lys Glu Lys Ile
Lys Glu Lys Leu
Lys Glu Leu Lys
Lys Ile Ala Trp
Lys Ile Glu Lys
Lys Ile Lys Glu
Lys Ile Arg Thr
Lys Ile Thr Arg
Lys Ile Trp Ala
Lys Lys Glu Ile
Lys Lys Glu Leu
Lys Lys Ile Glu
Lys Lys Lys Asn
Lys Lys Leu Glu
Lys Lys Asn Lys
Lys Lys Asn Gln
C21H40N8O7 (516.3019810000001)
Lys Lys Gln Asn
C21H40N8O7 (516.3019810000001)
Lys Leu Ala Trp
Lys Leu Glu Lys
Lys Leu Lys Glu
Lys Leu Arg Thr
Lys Leu Thr Arg
Lys Leu Trp Ala
Lys Asn Lys Lys
Lys Asn Lys Gln
C21H40N8O7 (516.3019810000001)
Lys Asn Gln Lys
C21H40N8O7 (516.3019810000001)
Lys Gln Lys Asn
C21H40N8O7 (516.3019810000001)
Lys Gln Asn Lys
C21H40N8O7 (516.3019810000001)
Lys Arg Asp Val
C21H40N8O7 (516.3019810000001)
Lys Arg Ile Thr
Lys Arg Leu Thr
Lys Arg Thr Ile
Lys Arg Thr Leu
Lys Arg Val Asp
C21H40N8O7 (516.3019810000001)
Lys Thr Ile Arg
Lys Thr Leu Arg
Lys Thr Arg Ile
Lys Thr Arg Leu
Lys Val Asp Arg
C21H40N8O7 (516.3019810000001)
Lys Val Arg Asp
C21H40N8O7 (516.3019810000001)
Lys Trp Ala Ile
Lys Trp Ala Leu
Lys Trp Ile Ala
Lys Trp Leu Ala
Leu Ala Lys Trp
Leu Ala Trp Lys
Leu Glu Lys Lys
Leu Lys Ala Trp
Leu Lys Glu Lys
Leu Lys Lys Glu
Leu Lys Arg Thr
Leu Lys Thr Arg
Leu Lys Trp Ala
Leu Gln Arg Thr
C21H40N8O7 (516.3019810000001)
Leu Gln Thr Arg
C21H40N8O7 (516.3019810000001)
Leu Arg Lys Thr
Leu Arg Gln Thr
C21H40N8O7 (516.3019810000001)
Leu Arg Thr Lys
Leu Arg Thr Gln
C21H40N8O7 (516.3019810000001)
Leu Thr Lys Arg
Leu Thr Gln Arg
C21H40N8O7 (516.3019810000001)
Leu Thr Arg Lys
Leu Thr Arg Gln
C21H40N8O7 (516.3019810000001)
Leu Trp Ala Lys
Leu Trp Lys Ala
Asn Lys Lys Lys
Asn Lys Lys Gln
C21H40N8O7 (516.3019810000001)
Asn Lys Gln Lys
C21H40N8O7 (516.3019810000001)
Asn Gln Lys Lys
C21H40N8O7 (516.3019810000001)
Gln Ile Arg Thr
C21H40N8O7 (516.3019810000001)
Gln Ile Thr Arg
C21H40N8O7 (516.3019810000001)
Gln Lys Lys Asn
C21H40N8O7 (516.3019810000001)
Gln Lys Asn Lys
C21H40N8O7 (516.3019810000001)
Gln Leu Arg Thr
C21H40N8O7 (516.3019810000001)
Gln Leu Thr Arg
C21H40N8O7 (516.3019810000001)
Gln Asn Lys Lys
C21H40N8O7 (516.3019810000001)
Gln Arg Ile Thr
C21H40N8O7 (516.3019810000001)
Gln Arg Leu Thr
C21H40N8O7 (516.3019810000001)
Gln Arg Thr Ile
C21H40N8O7 (516.3019810000001)
Gln Arg Thr Leu
C21H40N8O7 (516.3019810000001)
Gln Thr Ile Arg
C21H40N8O7 (516.3019810000001)
Gln Thr Leu Arg
C21H40N8O7 (516.3019810000001)
Gln Thr Arg Ile
C21H40N8O7 (516.3019810000001)
Gln Thr Arg Leu
C21H40N8O7 (516.3019810000001)
Arg Asp Lys Val
C21H40N8O7 (516.3019810000001)
Arg Asp Val Lys
C21H40N8O7 (516.3019810000001)
Arg Ile Lys Thr
Arg Ile Gln Thr
C21H40N8O7 (516.3019810000001)
Arg Ile Thr Lys
Arg Ile Thr Gln
C21H40N8O7 (516.3019810000001)
Arg Lys Asp Val
C21H40N8O7 (516.3019810000001)
Arg Lys Ile Thr
Arg Lys Leu Thr
Arg Lys Thr Ile
Arg Lys Thr Leu
Arg Lys Val Asp
C21H40N8O7 (516.3019810000001)
Arg Leu Lys Thr
Arg Leu Gln Thr
C21H40N8O7 (516.3019810000001)
Arg Leu Thr Lys
Arg Leu Thr Gln
C21H40N8O7 (516.3019810000001)
Arg Gln Ile Thr
C21H40N8O7 (516.3019810000001)
Arg Gln Leu Thr
C21H40N8O7 (516.3019810000001)
Arg Gln Thr Ile
C21H40N8O7 (516.3019810000001)
Arg Gln Thr Leu
C21H40N8O7 (516.3019810000001)
Arg Arg Ser Val
Arg Arg Val Ser
Arg Ser Arg Val
Arg Ser Val Arg
Arg Thr Ile Lys
Arg Thr Ile Gln
C21H40N8O7 (516.3019810000001)
Arg Thr Lys Ile
Arg Thr Lys Leu
Arg Thr Leu Lys
Arg Thr Leu Gln
C21H40N8O7 (516.3019810000001)
Arg Thr Gln Ile
C21H40N8O7 (516.3019810000001)
Arg Thr Gln Leu
C21H40N8O7 (516.3019810000001)
Arg Val Asp Lys
C21H40N8O7 (516.3019810000001)
Arg Val Lys Asp
C21H40N8O7 (516.3019810000001)
Arg Val Arg Ser
Arg Val Ser Arg
Ser Arg Arg Val
Ser Arg Val Arg
Ser Val Arg Arg
Thr Ile Lys Arg
Thr Ile Gln Arg
C21H40N8O7 (516.3019810000001)
Thr Ile Arg Lys
Thr Ile Arg Gln
C21H40N8O7 (516.3019810000001)
Thr Lys Ile Arg
Thr Lys Leu Arg
Thr Lys Arg Ile
Thr Lys Arg Leu
Thr Leu Lys Arg
Thr Leu Gln Arg
C21H40N8O7 (516.3019810000001)
Thr Leu Arg Lys
Thr Leu Arg Gln
C21H40N8O7 (516.3019810000001)
Thr Gln Ile Arg
C21H40N8O7 (516.3019810000001)
Thr Gln Leu Arg
C21H40N8O7 (516.3019810000001)
Thr Gln Arg Ile
C21H40N8O7 (516.3019810000001)
Thr Gln Arg Leu
C21H40N8O7 (516.3019810000001)
Thr Arg Ile Lys
Thr Arg Ile Gln
C21H40N8O7 (516.3019810000001)
Thr Arg Lys Ile
Thr Arg Lys Leu
Thr Arg Leu Lys
Thr Arg Leu Gln
C21H40N8O7 (516.3019810000001)
Thr Arg Gln Ile
C21H40N8O7 (516.3019810000001)
Thr Arg Gln Leu
C21H40N8O7 (516.3019810000001)
Val Asp Lys Arg
C21H40N8O7 (516.3019810000001)
Val Asp Arg Lys
C21H40N8O7 (516.3019810000001)
Val Lys Asp Arg
C21H40N8O7 (516.3019810000001)
Val Lys Arg Asp
C21H40N8O7 (516.3019810000001)
Val Arg Asp Lys
C21H40N8O7 (516.3019810000001)
Val Arg Lys Asp
C21H40N8O7 (516.3019810000001)
Val Arg Arg Ser
Val Arg Ser Arg
Val Ser Arg Arg
Trp Ala Ile Lys
Trp Ala Lys Ile
Trp Ala Lys Leu
Trp Ala Leu Lys
Trp Ile Ala Lys
Trp Ile Lys Ala
Trp Lys Ala Ile
Trp Lys Ala Leu
Trp Lys Ile Ala
Trp Lys Leu Ala
Trp Leu Ala Lys
Trp Leu Lys Ala
Phytolaccinic acid
Pokeberrygenin
GANODERIC ACID A
Ganoderic acid A can inhibit of the JAK-STAT3 signaling pathway, also inhibit proliferation, viability, ROS. Ganoderic acid A can inhibit of the JAK-STAT3 signaling pathway, also inhibit proliferation, viability, ROS.
Ganoderic acid B
Ganoderic acid B is a triterpene isolated from a mushroom Ganoderma lucidum. Ganoderic acid B inhibits the activation of Epstein-Barr virus (EBV) antigens as telomerase inhibitor. Ganoderic acid B is a moderately active inhibitor against HIV-1 protease[1][2][3]. Ganoderic acid B is a triterpene isolated from a mushroom Ganoderma lucidum. Ganoderic acid B inhibits the activation of Epstein-Barr virus (EBV) antigens as telomerase inhibitor. Ganoderic acid B is a moderately active inhibitor against HIV-1 protease[1][2][3].
Ganoderic acid D
ganoderic acid epsilon
ST 27:0;O9
1,4,7,10-Tetrakis(ethoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane
BOC-O-BENZYL-L-BETA-HOMOHYDROXYPROLINE DICYCLOHEXYLAMINE SALT
elatericin A
Cucurbitacin D is an active component in Trichosanthes kirilowii, disrupts interactions between Hsp90 and two co-chaperones, Cdc37 and p23. Cucurbitacin D prevents Hsp90 client (Her2, Raf, Cdk6, pAkt) maturation without induction of the heat shock response. Anti-cancer activity[1]. Cucurbitacin D is an active component in Trichosanthes kirilowii, disrupts interactions between Hsp90 and two co-chaperones, Cdc37 and p23. Cucurbitacin D prevents Hsp90 client (Her2, Raf, Cdk6, pAkt) maturation without induction of the heat shock response. Anti-cancer activity[1].
9-[(E)-3-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxy-5-[[3-[(2S,3S)-3-hydroxybutan-2-yl]oxiran-2-yl]methyl]oxan-2-yl]but-2-enoyl]oxynonanoic acid
(3S,8S,9R,10R,13R,14S,16R,17R)-17-[(E,2R)-2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl]-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-3,7,8,10,12,15,16,17-octahydrocyclopenta[a]phenanthren-11-one
(2E)-2-[(17E)-16-(acetyloxy)-3,11-dihydroxy-4,8,10,14-tetramethylgonan-17-ylidene]-6-methylhept-5-enoic acid
2-[hydroxy-[(2R)-2-hydroxy-3-[(6Z,9Z,12Z,15Z)-octadeca-6,9,12,15-tetraenoyl]oxypropoxy]phosphoryl]oxyethyl-trimethylazanium
(3beta,4alpha,5alpha,8alpha,9beta,11alpha)-3,8,11-Trihydroxy-4-methyl-1,6-dioxo-9,19-cycloergost-24(28)-ene-4-carboxylic acid
4-[[[(3S,6R,7S,8aS)-3-(4-acetamidobutyl)-6-(4-hydroxyphenyl)-1,4-dioxo-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazin-7-yl]-oxomethyl]amino]butyl-trimethylammonium
N-[(4S,7S,8S)-8-methoxy-4,7,10-trimethyl-5-[2-(4-morpholinyl)-1-oxoethyl]-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]cyclopropanecarboxamide
N-[(4R,7S,8R)-8-methoxy-4,7,10-trimethyl-5-(2-morpholin-4-ylacetyl)-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]cyclopropanecarboxamide
N-[(4S,7R,8R)-8-methoxy-4,7,10-trimethyl-5-(2-morpholin-4-ylacetyl)-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]cyclopropanecarboxamide
N-[(4R,7R,8S)-8-methoxy-4,7,10-trimethyl-5-[2-(4-morpholinyl)-1-oxoethyl]-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]cyclopropanecarboxamide
N-[(4R,7S,8S)-8-methoxy-4,7,10-trimethyl-5-(2-morpholin-4-ylacetyl)-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]cyclopropanecarboxamide
N-[(2S,3R)-2-[[cyclopropylmethyl(methyl)amino]methyl]-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-2,3,4,7-tetrahydro-1,5-benzoxazonin-9-yl]-3-(4-morpholinyl)propanamide
N-[(2R,3S)-2-[[cyclopropylmethyl(methyl)amino]methyl]-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-2,3,4,7-tetrahydro-1,5-benzoxazonin-9-yl]-3-(4-morpholinyl)propanamide
N-[(4S,7S,8R)-8-methoxy-4,7,10-trimethyl-5-[2-(4-morpholinyl)-1-oxoethyl]-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]cyclopropanecarboxamide
1-[(4S,7S,8R)-5-[cyclohexyl(oxo)methyl]-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propylurea
1-[(4R,7S,8S)-5-[cyclohexyl(oxo)methyl]-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propylurea
1-[(4S,7S,8S)-5-[cyclohexyl(oxo)methyl]-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propylurea
1-[(4S,7R,8S)-5-[cyclohexyl(oxo)methyl]-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propylurea
N-[(2S,3R)-2-[[cyclopropylmethyl(methyl)amino]methyl]-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-2,3,4,7-tetrahydro-1,5-benzoxazonin-9-yl]-3-(4-morpholinyl)propanamide
N-[(2R,3R)-2-[[cyclopropylmethyl(methyl)amino]methyl]-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-2,3,4,7-tetrahydro-1,5-benzoxazonin-9-yl]-3-(4-morpholinyl)propanamide
N-[(2R,3R)-2-[[cyclopropylmethyl(methyl)amino]methyl]-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-2,3,4,7-tetrahydro-1,5-benzoxazonin-9-yl]-3-(4-morpholinyl)propanamide
N-[(2S,3S)-2-[[cyclopropylmethyl(methyl)amino]methyl]-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-2,3,4,7-tetrahydro-1,5-benzoxazonin-9-yl]-3-(4-morpholinyl)propanamide
N-[(4S,7R,8S)-8-methoxy-4,7,10-trimethyl-5-[2-(4-morpholinyl)-1-oxoethyl]-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]cyclopropanecarboxamide
N-[(4R,7R,8R)-8-methoxy-4,7,10-trimethyl-5-[2-(4-morpholinyl)-1-oxoethyl]-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]cyclopropanecarboxamide
1-[(4S,7R,8R)-5-[cyclohexyl(oxo)methyl]-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propylurea
1-[(4R,7R,8S)-5-[cyclohexyl(oxo)methyl]-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propylurea
1-[(4R,7S,8R)-5-[cyclohexyl(oxo)methyl]-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propylurea
1-[(4R,7R,8R)-5-[cyclohexyl(oxo)methyl]-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propylurea
N-[(5S,6R,9R)-8-[cyclohexyl(oxo)methyl]-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-2-(dimethylamino)acetamide
2-[hydroxy-[(2R)-2-hydroxy-3-[(9E,11E,13E,15E)-octadeca-9,11,13,15-tetraenoyl]oxypropoxy]phosphoryl]oxyethyl-trimethylazanium
[2-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] (9E,12E)-octadeca-9,12-dienoate
[(4E,8E,12E)-3-hydroxy-2-(propanoylamino)octadeca-4,8,12-trienyl] 2-(trimethylazaniumyl)ethyl phosphate
[(4E,8E,12E)-2-(butanoylamino)-3-hydroxyheptadeca-4,8,12-trienyl] 2-(trimethylazaniumyl)ethyl phosphate
[(4E,8E,12E)-3-hydroxy-2-(pentanoylamino)hexadeca-4,8,12-trienyl] 2-(trimethylazaniumyl)ethyl phosphate
[(4E,8E,12E)-2-acetamido-3-hydroxynonadeca-4,8,12-trienyl] 2-(trimethylazaniumyl)ethyl phosphate
[(4E,8E,12E)-2-(hexanoylamino)-3-hydroxypentadeca-4,8,12-trienyl] 2-(trimethylazaniumyl)ethyl phosphate
[(4E,8E,12E)-2-(heptanoylamino)-3-hydroxytetradeca-4,8,12-trienyl] 2-(trimethylazaniumyl)ethyl phosphate
(6R)-6-((3S,5S,9S,10S,13S,14S,17R)-3-acetoxy-10,13-dimethyl-7,16-dioxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methylheptyl acetate
2-[hydroxy-[(2R)-2-hydroxy-3-[(6E,9E,12E,15E)-octadeca-6,9,12,15-tetraenoyl]oxypropoxy]phosphoryl]oxyethyl-trimethylazanium
2-[hydroxy-[2-hydroxy-3-[(6Z,9Z,12Z,15Z)-octadeca-6,9,12,15-tetraenoyl]oxypropoxy]phosphoryl]oxyethyl-trimethylazanium
2-[[2-acetyloxy-3-[(4Z,7Z,10Z,13Z)-hexadeca-4,7,10,13-tetraenoxy]propoxy]-hydroxyphosphoryl]oxyethyl-trimethylazanium
Cucurbitacin_D
Cucurbitacin D is a cucurbitacin in which a lanostane skeleton is multi-substituted with hydroxy, methyl and oxo substituents, with unsaturation at positions 5 and 23. It is a cucurbitacin, a secondary alpha-hydroxy ketone and a tertiary alpha-hydroxy ketone. It derives from a hydride of a lanostane. Cucurbitacin D is a natural product found in Elaeocarpus chinensis, Elaeocarpus hainanensis, and other organisms with data available. A cucurbitacin in which a lanostane skeleton is multi-substituted with hydroxy, methyl and oxo substituents, with unsaturation at positions 5 and 23. Cucurbitacin D is an active component in Trichosanthes kirilowii, disrupts interactions between Hsp90 and two co-chaperones, Cdc37 and p23. Cucurbitacin D prevents Hsp90 client (Her2, Raf, Cdk6, pAkt) maturation without induction of the heat shock response. Anti-cancer activity[1]. Cucurbitacin D is an active component in Trichosanthes kirilowii, disrupts interactions between Hsp90 and two co-chaperones, Cdc37 and p23. Cucurbitacin D prevents Hsp90 client (Her2, Raf, Cdk6, pAkt) maturation without induction of the heat shock response. Anti-cancer activity[1].
probucol
D057847 - Lipid Regulating Agents > D000960 - Hypolipidemic Agents > D000924 - Anticholesteremic Agents C - Cardiovascular system > C10 - Lipid modifying agents > C10A - Lipid modifying agents, plain C78276 - Agent Affecting Digestive System or Metabolism > C29703 - Antilipidemic Agent D020011 - Protective Agents > D000975 - Antioxidants D009676 - Noxae > D000963 - Antimetabolites
N-(5-aminopentyl)-N-hydroxy-N-{5-[hydroxy(4-{[5-(hydroxyimino)pentyl]amino}-4-oxobutanoyl)amino]pentyl}butanediamide
27-nor-campestan-3beta,4beta,5alpha,6alpha,7beta,8beta,14alpha,15alpha,24-nonol
FR171456
A steroid acid that is 9beta,19-cyclo-5alpha-ergost-24(28)-ene-4alpha-carboxylic acid which is substituted by hydroxy groups at the 3beta, 8alpha, and 11alpha positions, by a methyl group at the 4beta position, and by oxo groups at positions 1 and 6. It is a cholesterol and ergosterol synthesis inhibitor isolated from the fungus Sporormiella minima that specifically targets the enzyme, sterol-4-alpha-carboxylate-3-dehydrogenase, encoded by ERG26 in budding yeast, and NSDHL in humans.
3-O-(alpha-L-olivosyl)oleandolide
A macrolide that is oleandolide having a 2,6-dideoxy-alpha-L-arabino-hexopyranosyl (alpha-L-olivosyl) residue attached at position 3.