Exact Mass: 438.14606460000005
Exact Mass Matches: 438.14606460000005
Found 500 metabolites which its exact mass value is equals to given mass value 438.14606460000005,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Hamaudol 3-glucoside
C21H26O10 (438.15258960000006)
Sec-o-Glucosylhamaudol is a member of chromenes. sec-o-Glucosylhamaudol is a natural product found in Ostericum grosseserratum, Saposhnikovia divaricata, and other organisms with data available. Sec-O-Glucosylhamaudol is a natural compound extracted from Peucedanum japonicum Thunb, decreases levels of μ-opioid receptor, with analgesic effect[1]. Sec-O-Glucosylhamaudol is a natural compound extracted from Peucedanum japonicum Thunb, decreases levels of μ-opioid receptor, with analgesic effect[1]. Sec-O-Glucosylhamaudol is a natural compound extracted from Peucedanum japonicum Thunb, decreases levels of μ-opioid receptor, with analgesic effect[1].
Morusinol
Morusinol is a member of flavones. Morusinol is a natural product found in Morus lhou, Morus mongolica, and other organisms with data available. Morusinol is found in fruits. Morusinol is isolated from root bark of Morus alba (white mulberry Morusinol is a flavonoid isolated from Morus alba root bark. Morusinol has an antiplatelet activity and ?significantly inhibits arterial thrombosis in vivo[1]. Morusinol is a flavonoid isolated from Morus alba root bark. Morusinol has an antiplatelet activity and ?significantly inhibits arterial thrombosis in vivo[1].
Glaucolide B
C21H26O10 (438.15258960000006)
O-demethyl-N-demethyl-staurosporine
(2S)-2-amino-5-[[(2R)-1-(carboxymethylamino)-3-[(E)-N-hydroxy-C-(3-methylsulfanylpropyl)carbonimidoyl]sulfanyl-1-oxopropan-2-yl]amino]-5-oxopentanoic acid
7-Hydroxy-5-(4-hydroxy-2-oxopentyl)-2-methylchromone 7-glucoside
C21H26O10 (438.15258960000006)
7-Hydroxy-5-(4-hydroxy-2-oxopentyl)-2-methylchromone 7-glucoside is found in green vegetables. 7-Hydroxy-5-(4-hydroxy-2-oxopentyl)-2-methylchromone 7-glucoside is a constituent of Chinese rhubarb (Rheum sp.) Constituent of Chinese rhubarb (Rheum species). 7-Hydroxy-5-(4-hydroxy-2-oxopentyl)-2-methylchromone 7-glucoside is found in green vegetables.
Cnidimol 7-glucoside
C21H26O10 (438.15258960000006)
Constituent of Angelica archangelica (angelica). Cnidimol 7-glucoside is found in fats and oils, herbs and spices, and green vegetables. Cnidimol 7-glucoside is found in fats and oils. Cnidimol 7-glucoside is a constituent of Angelica archangelica (angelica).
Kanzonol T
Kanzonol T is found in herbs and spices. Kanzonol T is a constituent of Glycyrrhiza glabra (licorice)
Mulberranol
Mulberranol is found in fruits. Mulberranol is a constituent of the bark of Morus alba (white mulberry) (famine food)
2-{3,5-dihydroxy-9,13,13-trimethyl-8-oxatetracyclo[7.4.1.0(2),.0(1)(2),(1)]tetradeca-2(7),3,5-trien-4-yl}-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-4-one
1,6-Dihydroxy-3,7-dimethoxy-2-(3-methyl-2-butenyl)-8-(2-oxo-3-methyl-3-butenyl)-xanthone
1,6-Dihydroxy-3,7-dimethoxy-2-(3-methyl-2-butenyl)-8-(2-oxo-3-methyl-3-butenyl)-xanthone is found in fruits. 1,6-Dihydroxy-3,7-dimethoxy-2-(3-methyl-2-butenyl)-8-(2-oxo-3-methyl-3-butenyl)-xanthone is a constituent of the heartwood of Garcinia mangostana (mangosteen). Constituent of the heartwood of Garcinia mangostana (mangosteen). 1,6-Dihydroxy-3,7-dimethoxy-2-(3-methyl-2-butenyl)-8-(2-oxo-3-methyl-3-butenyl)-xanthone is found in fruits.
Albanin C
Albanin C is found in fruits. Albanin C is isolated from Morus alba (white mulberry) infected with Fusarium solani. Isolated from Morus alba (white mulberry) infected with Fusarium solani. Albanin C is found in fruits.
Artonin V
Artonin V is found in fruits. Artonin V is a constituent of the root bark of Artocarpus altilis (breadfruit). Constituent of the root bark of Artocarpus altilis (breadfruit). Artonin V is found in fruits.
(4S,6R)-6-[(1E)-4,4-Bis(4-fluorophenyl)-3-(1-methyltetrazol-5-yl)buta-1,3-dienyl]-4-hydroxyoxan-2-one
N-[(3R)-1-(2-Fluorophenyl)-4-oxo-3,4,6,7-tetrahydro[1,4]diazepino[6,7,1-hi]indol-3-yl]-1H-indole-2-carboxamide
(4S,7S,12Br)-6-oxo-7-[[(2S)-3-phenyl-2-sulfanylpropanoyl]amino]-2,3,4,7,8,12b-hexahydro-1H-pyrido[2,1-a][2]benzazepine-4-carboxylic acid
C24H26N2O4S (438.16131960000007)
Sec-o-Glucosylhamaudol
C21H26O10 (438.15258960000006)
Cichorioside K
C21H26O10 (438.15258960000006)
Cichorioside k is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Cichorioside k can be found in endive, which makes cichorioside k a potential biomarker for the consumption of this food product.
Isolupinisoflavone E
Villinol
Millewanin H
A hydroxyisoflavone that is isoflavone substituted by hydroxy groups at positions 5, 7, 3 and 4, a prenyl group at position 6 and a 2-hydroxy-3-methylbut-3-enyl moiety at position 8. Isolated from the leaves of Millettia pachycarpa, it exhibits antiestrogenic activity.
5,7-Dihydroxy-2-[4-hydroxy-3-(2-hydroxy-3-methyl-3-butenyl)phenyl]-6-(2-hydroxy-3-methyl-3-butenyl)-4H-1-benzopyran-4-one
Erysenegalensein H
8beta-Acetoxy-10beta-hydroxyhirsutinolide 1,13-O-diacetate
C21H26O10 (438.15258960000006)
Furowanin B
A hydroxyisoflavone that is 8,9-dihydro-4H-furo[2,3-h]chromen-4-one substituted by a hydroxy group at position 5, a 3,4-dihydroxyphenyl group at position 3, a 2-hydroxypropan-2-yl group at position 8 and a prenyl group at position 6. Isolated from Millettia pachycarpa, it exhibits anti-estrogenic activity.
Millewanin G
A member of the class of 7-hydroxyisoflavones that is isoflavone substituted by hydroxy groups at positions 5, 7, 3 and 4, a prenyl group at position 8 and a 2-hydroxy-3-methylbut-3-enyl moiety at position 6. Isolated from the leaves of Millettia pachycarpa, it exhibits antiestrogenic activity.
Kraussianone 3
Thonningin C
Broussonol C
Lupinisol B
1-Hydroxy-2,3-Epoxylupinifolin
1,10-Epoxy-14-hydroxyhypocretenolide beta-D-glucopyranoside
C21H26O10 (438.15258960000006)
Broussonol E
Papyriflavonol A is a pentahydroxyflavone that is flavone substituted with hydroxy groups at positions 3, 5, 7, 3 and 4 and prenyl groups at positions 6 and 5. Isolated from Broussonetia papyrifera, it exhibits inhibitory activity against phospholipase A2 and tyrosinase. It has a role as a metabolite, an EC 3.1.1.4 (phospholipase A2) inhibitor and an EC 1.14.18.1 (tyrosinase) inhibitor. It is a member of flavonols, a pentahydroxyflavone and a 3-hydroxyflavonoid. Broussonol E is a natural product found in Broussonetia papyrifera and Broussonetia kazinoki with data available. A pentahydroxyflavone that is flavone substituted with hydroxy groups at positions 3, 5, 7, 3 and 4 and prenyl groups at positions 6 and 5. Isolated from Broussonetia papyrifera, it exhibits inhibitory activity against phospholipase A2 and tyrosinase.
Broussonol D
[4R-(4R*,6S*,7R*,10R*)]-4,6-bis(Acetyloxy)-3-[(acetyloxy)methyl]-5,6,7,8,9,10-hexahydro-7-hydroxy-6,10-dimethyl-7,10-epoxycyclodeca[b]furan-2(4H)-one
C21H26O10 (438.15258960000006)
Morusignin L
Morusignin L is a member of flavones. Morusignin L is a natural product found in Morus insignis with data available.
Morusinol
Morusinol is a flavonoid isolated from Morus alba root bark. Morusinol has an antiplatelet activity and ?significantly inhibits arterial thrombosis in vivo[1]. Morusinol is a flavonoid isolated from Morus alba root bark. Morusinol has an antiplatelet activity and ?significantly inhibits arterial thrombosis in vivo[1].
4-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,6-dihydroxybenzoyl]-3-formyl-5-hydroxybenzoic acid
(2S,3R,4S)-5,7,3,4-tetrahydroxy-[2-methyl-2-(4-methyl-3-pentenyl)pyrano]-5,6,4-isoflavone
3,4,6-Tri-Ac-beta-D-4-Aminophenyl 2-acetamido-2-deoxyglucopyranoside
15-hydroxygermacra-1(10),4,11(13)-trien-(12,6);(14,8)-diolide 15-O-beta-D-glucopyranoside
C21H26O10 (438.15258960000006)
Benzyl 2,3,4,6-tetra-O-acetyl-b-D-glucopyranoside
C21H26O10 (438.15258960000006)
5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-8-(3-methylbut-2-en-1-yl)-6H-furo[2,3-c]xanthen-6-one
4-O-beta-D-Glucopyranoside-Secoeranthin
C21H26O10 (438.15258960000006)
Semicochliodinol B
A bisindole alkaloid that is quinone bearing hydroxy substituents at positions 2 and 5 and two indol-3-yl groups at positions 3 and 6, one of which is carrying a prenyl group at position 6. Isolated from the culture broth of Chrysosporium merdarium, it acts as an inhibitor of HIV-1 protease and EGF-R protein tyrosine kinase.
2,4-diacetoxy-1-(5-methoxy-8,8-dimethyl-3,4-dihydro-2H,8H-pyrano[3,2-g]chromen-3-yl)-benzene|Neoranflavan-diacetat
1,8,13-Tri-Ac-1,4-Epoxy-1,8,10,13-tetrahydroxy-5,7(11)-germacradien-12,6-olide
C21H26O10 (438.15258960000006)
3-(beta-D-glucopyranosyloxy)-7,7a-dihydro-6,7-dihydroxy-1a-(3-methyl-2-butenyl)naphth<2,3-b>oxiren-2(1aH)-one|3-(beta-D-glucopyranosyloxy)-7,7a-dihydro-6,7-dihydroxy-1a-(3-methyl-2-butenyl)naphth[2,3-b]oxiren-2(1aH)-one
C21H26O10 (438.15258960000006)
4-[4-hydroxyphenyl-(4-hydroxy-3-methoxybenzyl)]-3-(3,5-dihydroxyphenyl)-2-methoxy-tetrahydrofuran
(2E)-3-[3-(3,4-dihydroxybenzyl)-6-hydroxy-2,4-dimethoxyphenyl]-1-(3,4-dihydroxyphenyl)prop-2-en-1-one|3,4,6-trihydroxy-2,4-dimethoxy-3-(3,4-dihydroxybenzyl)chalcone
2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-6,8-bis(3-methylbut-2-enyl)chromen-4-one
5-((S)-2-oxo-4-hydroxypentyl)-2-(beta-glucopyranosyl-oxy-methyl)chromone
C21H26O10 (438.15258960000006)
2,4,5-trihydroxy-3-(3-methyl-2-butenyl)-(8,8-dimethyl-7-hydroxypyran)-(12,13;7,8)-flavone|hydroxymorusin|mornigrol G
4-hydroxy-5-(1-hydroxy-1-methyl)ethyl-dihydrofuran-(2,3:3,4)-5--prenyl-5,7-dihydroxyflavone
Dehydroascorbic acid-2,3-Bisbenzoylhydrazone, 5,6-di-Ac
D-Arabino-Hexose, 2-deoxy-, diethyl mercaptal, tetraacetate
2,3,6,8,9,12-Hexamethoxybenzo[1,2-b:4,5-b]bisbenzofuran
Furowanin A
2-(1-Methylethenyl)-3,4-dimethoxy-5-hydroxy-6-(3,4-dimethoxyphenyl)-7H-furo[3,2-g][1]benzopyran-7-one
1-Me ether,di-Ac-1,3,9-Trihydroxy-2-prenylpterocarpan
2alpha,3beta-dihydroxycyclohex-4-en-1beta-yl 2-O-[(E)-p-coumaroyl]-beta-D-glucopyranoside
C21H26O10 (438.15258960000006)
7-[(beta-D-glucopyranosyl)oxy]-5-hydroxy-8-[(2E)-4-hydroxy-3-methylbut-2-enyl]-2-methyl-4H-1-benzopyran-4-one
C21H26O10 (438.15258960000006)
Semicochliodinol A
A bisindole alkaloid that is quinone bearing hydroxy substituents at positions 2 and 5 and two indol-3-yl groups at positions 3 and 6, one of which is carrying a prenyl group at position 5. Isolated from the culture broth of Chrysosporium merdarium, it acts as an inhibitor of HIV-1 protease and EGF-R protein tyrosine kinase.
(E)-1-(glutathion-S-yl)-N-hydroxy-omega-(methylsulfanyl)butan-1-imine
Kushenol C
Kushenol C is a natural product found in Sophora flavescens and Gentiana macrophylla with data available.
MonnierisideG
C21H26O10 (438.15258960000006)
2-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,6-dihydroxybenzoyl]-5-formyl-3-hydroxybenzoic acid
4-hydroxy-7-methyl-2-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2,3-dihydrofuro[3,2-g]chromen-5-one
C21H26O10 (438.15258960000006)
2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-(2-hydroxy-3-methylbut-3-enyl)-3-(3-methylbut-2-enyl)chromen-4-one
4-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,6-dihydroxybenzoyl]-3-formyl-5-hydroxybenzoic acid
methyl 2-[[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]methyl]-3-(4-hydroxyphenyl)-4-methoxy-5-oxofuran-2-carboxylate
methyl 2-[[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]methyl]-3-(4-hydroxyphenyl)-4-methoxy-5-oxofuran-2-carboxylate
4-hydroxy-7-methyl-2-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2,3-dihydrofuro[3,2-g]chromen-5-one
C21H26O10 (438.15258960000006)
methyl 2-[[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]methyl]-3-(4-hydroxyphenyl)-4-methoxy-5-oxofuran-2-carboxylate [IIN-based on: CCMSLIB00000848627]
2-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,6-dihydroxybenzoyl]-5-formyl-3-hydroxybenzoic acid [IIN-based on: CCMSLIB00000848506]
methyl 2-[[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]methyl]-3-(4-hydroxyphenyl)-4-methoxy-5-oxofuran-2-carboxylate [IIN-based: Match]
2-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,6-dihydroxybenzoyl]-5-formyl-3-hydroxybenzoic acid [IIN-based: Match]
Losartan Metabolite (1H-Imidazole-2-propanol, 4-chloro-5-(hydroxymethyl)-a-methyl-1-[[2-(1H-tetrazo
Losartan Metabolite (1H-Imidazole-2,5-dimethanol, 4-chloro-a2-propyl-1-[[2-(1H-tetrazol-5-yl)[1,1-
Ala Cys Asp Met
Ala Cys Met Asp
Ala Asp Cys Met
Ala Asp Met Cys
Ala Met Cys Asp
Ala Met Asp Cys
Ala Met Met Ser
Ala Met Ser Met
Ala Ser Met Met
Cys Ala Asp Met
Cys Ala Met Asp
Cys Cys Asp Val
Cys Cys Ile Thr
Cys Cys Leu Thr
Cys Cys Thr Ile
Cys Cys Thr Leu
Cys Cys Val Asp
Cys Asp Ala Met
Cys Asp Cys Val
Cys Asp Met Ala
Cys Asp Thr Thr
C15H26N4O9S (438.1420426000001)
Cys Asp Val Cys
Cys Glu Gly Met
Cys Glu Met Gly
Cys Glu Ser Thr
C15H26N4O9S (438.1420426000001)
Cys Glu Thr Ser
C15H26N4O9S (438.1420426000001)
Cys Gly Glu Met
Cys Gly Met Glu
Cys Gly Pro Tyr
C19H26N4O6S (438.15729760000005)
Cys Gly Tyr Pro
C19H26N4O6S (438.15729760000005)
Cys Ile Cys Thr
Cys Ile Thr Cys
Cys Leu Cys Thr
Cys Leu Thr Cys
Cys Met Ala Asp
Cys Met Asp Ala
Cys Met Glu Gly
Cys Met Gly Glu
Cys Met Ser Val
Cys Met Val Ser
Cys Pro Gly Tyr
C19H26N4O6S (438.15729760000005)
Cys Pro Tyr Gly
C19H26N4O6S (438.15729760000005)
Cys Ser Glu Thr
C15H26N4O9S (438.1420426000001)
Cys Ser Met Val
Cys Ser Thr Glu
C15H26N4O9S (438.1420426000001)
Cys Ser Val Met
Cys Thr Cys Ile
Cys Thr Cys Leu
Cys Thr Asp Thr
C15H26N4O9S (438.1420426000001)
Cys Thr Glu Ser
C15H26N4O9S (438.1420426000001)
Cys Thr Ile Cys
Cys Thr Leu Cys
Cys Thr Ser Glu
C15H26N4O9S (438.1420426000001)
Cys Thr Thr Asp
C15H26N4O9S (438.1420426000001)
Cys Val Cys Asp
Cys Val Asp Cys
Cys Val Met Ser
Cys Val Ser Met
Cys Tyr Gly Pro
C19H26N4O6S (438.15729760000005)
Cys Tyr Pro Gly
C19H26N4O6S (438.15729760000005)
Asp Ala Cys Met
Asp Ala Met Cys
Asp Cys Ala Met
Asp Cys Cys Val
Asp Cys Met Ala
Asp Cys Thr Thr
C15H26N4O9S (438.1420426000001)
Asp Cys Val Cys
Asp Met Ala Cys
Asp Met Cys Ala
Asp Met Ser Ser
C15H26N4O9S (438.1420426000001)
Asp Ser Met Ser
C15H26N4O9S (438.1420426000001)
Asp Ser Ser Met
C15H26N4O9S (438.1420426000001)
Asp Thr Cys Thr
C15H26N4O9S (438.1420426000001)
Asp Thr Thr Cys
C15H26N4O9S (438.1420426000001)
Asp Val Cys Cys
Glu Cys Gly Met
Glu Cys Met Gly
Glu Cys Ser Thr
C15H26N4O9S (438.1420426000001)
Glu Cys Thr Ser
C15H26N4O9S (438.1420426000001)
Glu Gly Cys Met
Glu Gly Met Cys
Glu Met Cys Gly
Glu Met Gly Cys
Glu Ser Cys Thr
C15H26N4O9S (438.1420426000001)
Glu Ser Thr Cys
C15H26N4O9S (438.1420426000001)
Glu Thr Cys Ser
C15H26N4O9S (438.1420426000001)
Glu Thr Ser Cys
C15H26N4O9S (438.1420426000001)
Gly Cys Glu Met
Gly Cys Met Glu
Gly Cys Pro Tyr
C19H26N4O6S (438.15729760000005)
Gly Cys Tyr Pro
C19H26N4O6S (438.15729760000005)
Gly Glu Cys Met
Gly Glu Met Cys
Gly Met Cys Glu
Gly Met Glu Cys
Gly Met Met Thr
Gly Met Thr Met
Gly Pro Cys Tyr
C19H26N4O6S (438.15729760000005)
Gly Pro Tyr Cys
C19H26N4O6S (438.15729760000005)
Gly Thr Met Met
Gly Tyr Cys Pro
C19H26N4O6S (438.15729760000005)
Gly Tyr Pro Cys
C19H26N4O6S (438.15729760000005)
Ile Cys Cys Thr
Ile Cys Thr Cys
Ile Thr Cys Cys
Leu Cys Cys Thr
Leu Cys Thr Cys
Leu Thr Cys Cys
Met Ala Cys Asp
Met Ala Asp Cys
Met Ala Met Ser
Met Ala Ser Met
Met Cys Ala Asp
Met Cys Asp Ala
Met Cys Glu Gly
Met Cys Gly Glu
Met Cys Ser Val
Met Cys Val Ser
Met Asp Ala Cys
Met Asp Cys Ala
Met Asp Ser Ser
C15H26N4O9S (438.1420426000001)
Met Glu Cys Gly
Met Glu Gly Cys
Met Gly Cys Glu
Met Gly Glu Cys
Met Gly Met Thr
Met Gly Thr Met
Met Met Ala Ser
Met Met Gly Thr
Met Met Ser Ala
Met Met Thr Gly
Met Ser Ala Met
Met Ser Cys Val
Met Ser Asp Ser
C15H26N4O9S (438.1420426000001)
Met Ser Met Ala
Met Ser Ser Asp
C15H26N4O9S (438.1420426000001)
Met Ser Val Cys
Met Thr Gly Met
Met Thr Met Gly
Met Val Cys Ser
Met Val Ser Cys
Pro Cys Gly Tyr
C19H26N4O6S (438.15729760000005)
Pro Cys Tyr Gly
C19H26N4O6S (438.15729760000005)
Pro Gly Cys Tyr
C19H26N4O6S (438.15729760000005)
Pro Gly Tyr Cys
C19H26N4O6S (438.15729760000005)
Pro Tyr Cys Gly
C19H26N4O6S (438.15729760000005)
Pro Tyr Gly Cys
C19H26N4O6S (438.15729760000005)
Ser Ala Met Met
Ser Cys Glu Thr
C15H26N4O9S (438.1420426000001)
Ser Cys Met Val
Ser Cys Thr Glu
C15H26N4O9S (438.1420426000001)
Ser Cys Val Met
Ser Asp Met Ser
C15H26N4O9S (438.1420426000001)
Ser Asp Ser Met
C15H26N4O9S (438.1420426000001)
Ser Glu Cys Thr
C15H26N4O9S (438.1420426000001)
Ser Glu Thr Cys
C15H26N4O9S (438.1420426000001)
Ser Met Ala Met
Ser Met Cys Val
Ser Met Asp Ser
C15H26N4O9S (438.1420426000001)
Ser Met Met Ala
Ser Met Ser Asp
C15H26N4O9S (438.1420426000001)
Ser Met Val Cys
Ser Ser Asp Met
C15H26N4O9S (438.1420426000001)
Ser Ser Met Asp
C15H26N4O9S (438.1420426000001)
Ser Thr Cys Glu
C15H26N4O9S (438.1420426000001)
Ser Thr Glu Cys
C15H26N4O9S (438.1420426000001)
Ser Val Cys Met
Ser Val Met Cys
Thr Cys Cys Ile
Thr Cys Cys Leu
Thr Cys Asp Thr
C15H26N4O9S (438.1420426000001)
Thr Cys Glu Ser
C15H26N4O9S (438.1420426000001)
Thr Cys Ile Cys
Thr Cys Leu Cys
Thr Cys Ser Glu
C15H26N4O9S (438.1420426000001)
Thr Cys Thr Asp
C15H26N4O9S (438.1420426000001)
Thr Asp Cys Thr
C15H26N4O9S (438.1420426000001)
Thr Asp Thr Cys
C15H26N4O9S (438.1420426000001)
Thr Glu Cys Ser
C15H26N4O9S (438.1420426000001)
Thr Glu Ser Cys
C15H26N4O9S (438.1420426000001)
Thr Gly Met Met
Thr Ile Cys Cys
Thr Leu Cys Cys
Thr Met Gly Met
Thr Met Met Gly
1-[[2-(2,3-dihydro-2-oxo-1H-indol-4-yl)ethyl]propylcarbamate] glucuronide
Thr Ser Cys Glu
C15H26N4O9S (438.1420426000001)
Thr Ser Glu Cys
C15H26N4O9S (438.1420426000001)
Thr Thr Cys Asp
C15H26N4O9S (438.1420426000001)
Thr Thr Asp Cys
C15H26N4O9S (438.1420426000001)
Val Cys Cys Asp
Val Cys Asp Cys
Val Cys Met Ser
Val Cys Ser Met
Val Asp Cys Cys
Val Met Cys Ser
Val Met Ser Cys
Val Ser Cys Met
Val Ser Met Cys
Tyr Cys Gly Pro
C19H26N4O6S (438.15729760000005)
Tyr Cys Pro Gly
C19H26N4O6S (438.15729760000005)
Tyr Gly Cys Pro
C19H26N4O6S (438.15729760000005)
Tyr Gly Pro Cys
C19H26N4O6S (438.15729760000005)
Tyr Pro Cys Gly
C19H26N4O6S (438.15729760000005)
Tyr Pro Gly Cys
C19H26N4O6S (438.15729760000005)
Kanzonol T
Mulberranol
Albanin C
7-Hydroxy-5-(4-hydroxy-2-oxopentyl)-2-methylchromone 7-glucoside
C21H26O10 (438.15258960000006)
1,6-Dihydroxy-3,7-dimethoxy-2-(3-methyl-2-butenyl)-8-(2-oxo-3-methyl-3-butenyl)-xanthone
Cnidimol 7-glucoside
C21H26O10 (438.15258960000006)
Artonin V
Methyl 2-[4-hydroxy-3-(3-methyl-2-buten-1-yl)benzyl]-3-(4-hydroxyphenyl)-4-methoxy-5-oxo-2,5-dihydro-2-furancarboxylate
2-(4-Hydroxy-7-methyl-5-oxo-2,3-dihydro-5H-furo[3,2-g]chromen-2-yl)-2-propanyl hexopyranoside
C21H26O10 (438.15258960000006)
4-[2-BUTYL-5-(2-METHOXYCARBONYL-3-THIOPHEN-2-YL-PROPENYL)-IMIDAZOL-1-YLMETHYL]-BENZOIC ACID
C24H26N2O4S (438.16131960000007)
[(2R,3R,4S,5R,6S)-3,5,6-triacetyloxy-4-phenylmethoxyoxan-2-yl]methyl acetate
C21H26O10 (438.15258960000006)
2-[2,6-di(propan-2-yl)phenyl]-5-methylimidazo[1,5-a]pyridin-4-ium,hexafluorophosphate
Dolasetron (Mesylate hydrate)
C20H26N2O7S (438.14606460000005)
Dolasetron Mesylate hydrate (MDL-73147EF hydrate) is a serotonin 5-HT3 receptor antagonist used to treat nausea and vomiting following chemotherapy.
Phenyl 2,4,6-Tri-O-acetyl-3-O-allyl-1-thio-beta-D-glucopyranoside
C21H26O8S (438.13483160000004)
4,4-BIS(DIMETHYLAMINO)-4-METHOXY-3-SULFOTRITYL INNER SALT
C24H26N2O4S (438.16131960000007)
L-Aspartic acid,N-[4-[[(2,4-diamino-5-methyl-6-quinazolinyl)methyl]amino]benzoyl]-
1-chloro-Tri-2,3,5-O-benzyl-D-arabofuranose
C26H27ClO4 (438.15977720000006)
1-(3,4-difluorophenyl)-7,7-dimethyl-3-[(3-nitrophenyl)methyl]-6,8-dihydroquinoline-2,5-dione
C24H20F2N2O4 (438.13910640000006)
Methyl 1-C-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-alpha-D-glucopyranoside
C22H27ClO7 (438.14452220000004)
Fmoc-L-1,2,3,4-Tetrahydronorharman-3-carboxylic acid
fmoc-d-1,2,3,4-tetrahydronorharman-3-carboxylic acid
Benzenesulfonamide, N-[(1S)-2-amino[1,1-binaphthalen]-2-yl]-4-methyl
Bruceolide
C21H26O10 (438.15258960000006)
A quassinoid isolated from Brucea javanica and Brucea sumatrana and has been shown to exhibit antimalarial activity.
N-(2-CYANO-4-OXO-4H-CHROMEN-8-YL)-4-(4-PHENYLBUTOXY)BENZAMIDE
(2S)-2-[[5-[3-(2,6-diamino-4-oxo-1H-pyrimidin-5-yl)propylamino]thiophene-2-carbonyl]amino]pentanedioic acid
4-[5-(4-Methoxyphenyl)-2-oxazolyl]-1-methylpyridinium 4-methylbenzenesulfonate
C23H22N2O5S (438.12493620000004)
Benzyl 2,3,4,6-Tetra-O-acetyl--D-Glucopyranoside
C21H26O10 (438.15258960000006)
2,5-Bis(octyldithio)-1,3,4-thiadiazole
C18H34N2S5 (438.13254440000003)
Mibampator
C26170 - Protective Agent > C1509 - Neuroprotective Agent Mibampator (LY451395) is a potent and highly selective potentiator of the AMPA receptors.
7-(4-Fluoro-2-methoxyphenyl)-6-methyl-N-(1-(piperidin-4-yl)-1H-pyrazol-4-yl) thieno (3,2-d)pyrimidin-2-amine
C274 - Antineoplastic Agent > C2189 - Signal Transduction Inhibitor > C129824 - Antineoplastic Protein Inhibitor C274 - Antineoplastic Agent > C163758 - Targeted Therapy Agent > C163790 - Flt-3-targeting Agent C274 - Antineoplastic Agent > C163758 - Targeted Therapy Agent > C164035 - FGFR-targeting Agent C471 - Enzyme Inhibitor > C1404 - Protein Kinase Inhibitor > C1967 - Tyrosine Kinase Inhibitor C471 - Enzyme Inhibitor > C129825 - Antineoplastic Enzyme Inhibitor > C155727 - FGFR Inhibitor
1H-Isoindol-1-one, 2-((1-(2-(4-fluorophenyl)-2-oxoethyl)-4-piperidinyl)methyl)-2,3-dihydro-, hydrochloride, hydrate (1:1:2)
C22H28ClFN2O4 (438.17215300000004)
C78272 - Agent Affecting Nervous System > C29710 - Antipsychotic Agent
2,5-Cyclohexadiene-1,4-dione, 2-(2-(1,1-dimethyl-2-propenyl)-1H-indol-3-yl)-3,6-dihydroxy-5-(1H-indol-3-yl)-
Spiraprilat
C20H26N2O5S2 (438.12830660000003)
An azaspiro compound that is spirapril in which the ethyl ester group has been hydrolysed to the corresponding carboxylic acid group. It is the active metabolite of the angiotensin-converting enzyme (ACE) inhibitor spirapril. C78274 - Agent Affecting Cardiovascular System > C270 - Antihypertensive Agent C471 - Enzyme Inhibitor > C783 - Protease Inhibitor > C247 - ACE Inhibitor
Bis(trimethylsilyl) 2,3-bis[(trimethylsilyl)oxy]succinate
(2s)-3-(1-{[2-(2-Chlorophenyl)-5-Methyl-1,3-Oxazol-4-Yl]methyl}-1h-Indol-5-Yl)-2-Ethoxypropanoic Acid
C24H23ClN2O4 (438.13462680000004)
6-[(1E)-4,4-bis(4-fluorophenyl)-3-(1-methyltetrazol-5-yl)buta-1,3-dienyl]-4-hydroxyoxan-2-one
6-[4-methoxy-3-(3-oxolanyloxy)phenyl]-3-(2-methoxyphenyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine
C22H22N4O4S (438.13616920000004)
2-Cyano-3-(1-{[(furan-2-ylmethyl)-carbamoyl]-methyl}-1H-indol-3-yl)-N-m-tolyl-acrylamide
5-[2-[[2-[[2-furanyl(oxo)methyl]amino]phenyl]-oxomethoxy]-1-oxoethyl]-2,4-dimethyl-1H-pyrrole-3-carboxylic acid ethyl ester
6-[4,6-bis(4-methoxyphenyl)-2-pyridinyl]-4H-1,4-benzoxazin-3-one
ethyl 4-[6-(4-oxo-2-sulfanylidene-1H-thieno[3,2-d]pyrimidin-3-yl)hexanoyl]piperazine-1-carboxylate
C19H26N4O4S2 (438.13953960000003)
3-chloro-N-[2-[4-(4-fluorophenyl)-1-piperazinyl]-2-(3-pyridinyl)ethyl]benzamide
5-(2-Hydroxy-3,4-dimethyl-phenyl)-2H-pyrazole-3-carboxylic acid (3-ethylcarbamoyl-4,5,6,7-tetrahydro-benzo[b]thiophen-2-yl)-amide
(4E)-1-acetyl-6-hydroxyspiro[chromene-2,4-piperidin]-4(3H)-one N-(4-methylphenyl)thiosemicarbazone
2-[3-(4-methylphenyl)-6,7-dihydro-5H-pyrrolo[1,2-a]imidazol-1-ium-1-yl]-1-(10-phenothiazinyl)ethanone
(1S,5R)-7-[4-(3-pyridinyl)phenyl]-N-[4-(trifluoromethyl)phenyl]-3,6-diazabicyclo[3.1.1]heptane-3-carboxamide
(1S,5R)-7-[4-(2-fluorophenyl)phenyl]-3-(3-methoxyphenyl)sulfonyl-3,6-diazabicyclo[3.1.1]heptane
C24H23FN2O3S (438.14133400000003)
(1S,5R)-N-(1,3-benzodioxol-5-yl)-7-[4-(4-cyanophenyl)phenyl]-3,6-diazabicyclo[3.1.1]heptane-3-carboxamide
(1S,5R)-3-(2-fluorophenyl)sulfonyl-7-[4-(3-methoxyphenyl)phenyl]-3,6-diazabicyclo[3.1.1]heptane
C24H23FN2O3S (438.14133400000003)
(6S,7S,8S)-4-(benzenesulfonyl)-8-(hydroxymethyl)-7-[4-(3-methylbut-1-ynyl)phenyl]-1,4-diazabicyclo[4.2.0]octan-2-one
C24H26N2O4S (438.16131960000007)
(6R,7S,8S)-4-(benzenesulfonyl)-8-(hydroxymethyl)-7-[4-(3-methylbut-1-ynyl)phenyl]-1,4-diazabicyclo[4.2.0]octan-2-one
C24H26N2O4S (438.16131960000007)
(1R,5S)-6-(4-fluorophenyl)sulfonyl-7-[4-(2-methoxyphenyl)phenyl]-3,6-diazabicyclo[3.1.1]heptane
C24H23FN2O3S (438.14133400000003)
(6S,7R,8R)-4-(benzenesulfonyl)-8-(hydroxymethyl)-7-[4-(3-methylbut-1-ynyl)phenyl]-1,4-diazabicyclo[4.2.0]octan-2-one
C24H26N2O4S (438.16131960000007)
(6R,7R,8S)-4-(benzenesulfonyl)-8-(hydroxymethyl)-7-[4-(3-methylbut-1-ynyl)phenyl]-1,4-diazabicyclo[4.2.0]octan-2-one
C24H26N2O4S (438.16131960000007)
(6S,7S,8R)-4-(benzenesulfonyl)-8-(hydroxymethyl)-7-[4-(3-methylbut-1-ynyl)phenyl]-1,4-diazabicyclo[4.2.0]octan-2-one
C24H26N2O4S (438.16131960000007)
(6S,7R,8S)-4-(benzenesulfonyl)-8-(hydroxymethyl)-7-[4-(3-methylbut-1-ynyl)phenyl]-1,4-diazabicyclo[4.2.0]octan-2-one
C24H26N2O4S (438.16131960000007)
(2R,3R)-cis-delta-viniferin
A stilbenoid that is the (2R,3R)-cis-stereoisomer of delta-viniferin, obtained by cyclodimerisation of cis-resveratrol.
(2S,3S)-cis-delta-viniferin
A stilbenoid that is the (2S,3S)-cis-stereoisomer of delta-viniferin, obtained by cyclodimerisation of cis-resveratrol.
5,7-Dihydroxy-2-[7-hydroxy-2-(hydroxymethyl)-2-(4-methylpent-3-enyl)chromen-6-yl]-2,3-dihydrochromen-4-one
2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-8-(2-hydroxy-3-methylbut-3-enyl)-3-(3-methylbut-2-enyl)chromen-4-one
[(1S,2S,4R,8R)-8,10-diacetyloxy-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-11-en-12-yl]methyl acetate
C21H26O10 (438.15258960000006)
(4S,5R,6R)-6-[(1S)-1-hydroxyethyl]-4-methyl-7-oxo-3-[(3S,5S)-5-[(sulfamoylamino)methyl]pyrrolidin-3-yl]sulfanyl-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid;hydrate
2,5-Bis(2,5-dimethoxybenzyloxy)-2,4,6-cycloheptatrien-1-one
2-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,6-dihydroxybenzoyl]-5-formyl-3-hydroxybenzoic acid
Hamaudol 3-glucoside
C21H26O10 (438.15258960000006)
Sec-o-Glucosylhamaudol is a member of chromenes. sec-o-Glucosylhamaudol is a natural product found in Ostericum grosseserratum, Saposhnikovia divaricata, and other organisms with data available. Sec-O-Glucosylhamaudol is a natural compound extracted from Peucedanum japonicum Thunb, decreases levels of μ-opioid receptor, with analgesic effect[1]. Sec-O-Glucosylhamaudol is a natural compound extracted from Peucedanum japonicum Thunb, decreases levels of μ-opioid receptor, with analgesic effect[1]. Sec-O-Glucosylhamaudol is a natural compound extracted from Peucedanum japonicum Thunb, decreases levels of μ-opioid receptor, with analgesic effect[1].
Asterriquinone C1
A bisindole alkaloid that is quinone bearing two hydroxy substituents at position 2 and 5 and two indol-3-yl groups at positions 3 and 6, one of which is carrying a 1,1-dimethylallyl group at position 2; major microspecies at pH 7.3.
(+)-kotanin
A member of the class of 8,8-bicoumarins resulting from the formal oxidative dimerisation of 4,7-dimethoxy-5-methyl-2H-chromen-2-one (the S-(+) enantiomer). A fungal metabolite, its isolation from Aspergillus clavatus was first reported in 1971.
SIRT2-IN-9
SIRT2-IN-9 (compound 12) is a selective inhibitor of SRIT2 with an IC50 value of 1.3 μM. SIRT2-IN-9 inhibits proliferative activity of MCF-7 breast cancer cells. SIRT2-IN-9 can be used for the research of cancer[1].
(8z)-2,16-dioxapentacyclo[22.2.2.1³,⁷.1¹⁷,²¹.0¹⁰,¹⁵]triaconta-1(26),3(30),4,6,8,10,12,14,17(29),18,20,24,27-tridecaene-4,12,22-triol
3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-(2-hydroxy-3-methylbut-3-en-1-yl)-8-(3-methylbut-2-en-1-yl)chromen-4-one
2-[(8ar,10as)-4-hydroxy-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5h-xanthen-1-yl]-3,5,7-trihydroxychromen-4-one
2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-8-[(2s)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]chromen-4-one
20,28-dihydroxy-4,11,18,25-tetraazaheptacyclo[14.11.1.0²,¹⁵.0³,¹².0⁵,¹⁰.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-2(15),3,5,7,9,11,13,17(26),20,22,24-undecaene-9-carboxylic acid
(1s,10r)-1,4,6,14-tetrahydroxy-5,10-bis(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-3,5,7,11,13,15-hexaen-2-one
[(9r)-3,15-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-yl]oxidanesulfonic acid
C21H26O8S (438.13483160000004)
ethyl (2s)-4-[(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methyl]-2-hydroxy-3-(4-hydroxyphenyl)-5-oxofuran-2-carboxylate
(1r,2r,8r,10r,14s,17r,18r)-17-(furan-3-yl)-2,7,7,18-tetramethyl-6,9,16-trioxapentacyclo[11.7.0.0²,⁸.0⁸,¹⁰.0¹⁴,¹⁸]icosa-3,12-diene-5,11,15-trione
5,7',8-trihydroxy-6-(3-hydroxy-3-methylbutyl)-2',2'-dimethyl-[3,6'-bichromen]-4-one
(1s,2r,6r,7z,11e)-3-methylidene-8-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-5,14-dioxatricyclo[10.2.1.0²,⁶]pentadeca-7,11-diene-4,13-dione
C21H26O10 (438.15258960000006)
4,4',7,7'-tetramethoxy-5,5'-dimethyl-[6,8'-bichromene]-2,2'-dione
[(1s,2e,8r,10s,11r)-8,10-bis(acetyloxy)-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-6-yl]methyl acetate
C21H26O10 (438.15258960000006)
(2e)-1-(3,4-dihydroxyphenyl)-3-{3-[(3,4-dihydroxyphenyl)methyl]-6-hydroxy-2,4-dimethoxyphenyl}prop-2-en-1-one
6-{3-[(1r)-3-ethoxy-1-(4-hydroxyphenyl)but-3-en-1-yl]-4,6-dihydroxy-2-methylphenyl}-4-methoxypyran-2-one
(2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-{[(1r,3r,4s)-4,8,10-trihydroxy-1,3-dimethyl-1h,3h,4h-naphtho[2,3-c]pyran-7-yl]oxy}oxane-3,4,5-triol
C21H26O10 (438.15258960000006)
(9r)-3-(2,4-dihydroxyphenyl)-5,9-dihydroxy-8,8-dimethyl-6-(3-methylbut-2-en-1-yl)-9h,10h-pyrano[2,3-h]chromen-4-one
methyl 4a,5,6,7-tetrahydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate
C17H26O13 (438.13733460000003)
methyl (2e,4r,5r,6e)-7-{2-[2-(2-hydroxypropan-2-yl)-1,3-thiazol-4-yl]-1,3-thiazol-4-yl}-3,5-dimethoxy-4-methylhepta-2,6-dienoate
C20H26N2O5S2 (438.12830660000003)
4-hydroxy-2,15-dioxapentacyclo[22.2.2.1³,⁷.1¹⁰,¹⁴.0¹⁶,²¹]triaconta-1(26),3(30),4,6,10,12,14(29),16(21),18,24,27-undecaene-17,20-dione
2-(hydroxymethyl)-6-({4,8,10-trihydroxy-1,3-dimethyl-1h,3h,4h-naphtho[2,3-c]pyran-7-yl}oxy)oxane-3,4,5-triol
C21H26O10 (438.15258960000006)