Exact Mass: 346.0399
Exact Mass Matches: 346.0399
Found 371 metabolites which its exact mass value is equals to given mass value 346.0399
,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
6-Methoxy-7-methylquercetin
6-methoxy-7-methylquercetin, also known as eupatoletin, is a member of the class of compounds known as flavonols. Flavonols are compounds that contain a flavone (2-phenyl-1-benzopyran-4-one) backbone carrying a hydroxyl group at the 3-position. Thus, 6-methoxy-7-methylquercetin is considered to be a flavonoid lipid molecule. 6-methoxy-7-methylquercetin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 6-methoxy-7-methylquercetin can be found in german camomile, which makes 6-methoxy-7-methylquercetin a potential biomarker for the consumption of this food product. Eupatolitin is a tetrahydroxyflavone that is flavone substituted by hydroxy groups at positions 3, 5, 3 and 4 and methoxy groups at positions 6 and 7 respectively. It is a tetrahydroxyflavone, a dimethoxyflavone and a member of flavonols. It is functionally related to a flavone. Eupatolitin is a natural product found in Dicoma tomentosa, Haplopappus foliosus, and other organisms with data available.
DIBOA trihexose
Syringetin,?a flavonoid derivative, is associated with increased BMP-2 production. Syringetin stimulates osteoblast differentiation at various stages, from maturation to terminally differentiated osteoblasts[1]. Syringetin,?a flavonoid derivative, is associated with increased BMP-2 production. Syringetin stimulates osteoblast differentiation at various stages, from maturation to terminally differentiated osteoblasts[1].
Aflatoxin B1 diol
This compound belongs to the family of Difurocoumarocyclopentenone Series. These are polycyclic aromatic compounds containing a cyclopenten-2-one ring fused to the coumarin moiety of the difurocoumarin skeleton. Difurocoumarocyclopentenones are a subgroup of the aflatoxins and related compounds D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D011042 - Poisons > D000348 - Aflatoxins
Aflatoxin B1 dialdehyde
Limocitrin
Limocitrin is a hydroxyflavan. Limocitrin is a natural product found in Sedum anglicum, Sedum forsterianum, and other organisms with data available. Limocitrin is found in citrus. Limocitrin is a constituent of citrus fruit peels Constituent of citrus fruit peels. Limocitrin is found in lemon and citrus.
Syringetin
Syringetin is a dimethoxyflavone that is myricetin in which the hydroxy groups at positions 3 and 5 have been replaced by methoxy groups. It has a role as a platelet aggregation inhibitor and a metabolite. It is a tetrahydroxyflavone, a dimethoxyflavone, a 7-hydroxyflavonol, a member of 3-methoxyflavones and a 3,5-dimethoxyflavone. It is functionally related to a myricetin. It is a conjugate acid of a syringetin(1-). Syringetin is a natural product found in Lysimachia congestiflora, Chondropetalum, and other organisms with data available. A dimethoxyflavone that is myricetin in which the hydroxy groups at positions 3 and 5 have been replaced by methoxy groups. Syringetin,?a flavonoid derivative, is associated with increased BMP-2 production. Syringetin stimulates osteoblast differentiation at various stages, from maturation to terminally differentiated osteoblasts[1]. Syringetin,?a flavonoid derivative, is associated with increased BMP-2 production. Syringetin stimulates osteoblast differentiation at various stages, from maturation to terminally differentiated osteoblasts[1].
Spinacetin
Isolated from spinach (Spinacia oleracea). Spinacetin is found in german camomile, green vegetables, and spinach. Spinacetin is found in german camomile. Spinacetin is isolated from spinach (Spinacia oleracea
6-(4-carboxy-2,6-dihydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid
6-(4-carboxy-2,6-dihydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 3,4,5-trihydroxybenzoic acid. It is generated by UDP-glucuronosyltransferase 1-1 (P22309) enzyme via an aromatic-OH-glucuronidation reaction. This aromatic-OH-glucuronidation occurs in humans.
3,3'-Bisjuglone
3,3-Bisjuglone is found in nuts. 3,3-Bisjuglone is a constituent of Juglans regia (walnut). Constituent of Juglans regia (walnut). 3,3-Bisjuglone is found in nuts.
3,4,5-trihydroxy-6-(3,4,5-trihydroxybenzoyloxy)oxane-2-carboxylic acid
Aflatoxin G2a
Aflatoxin G2a is a minor mycotoxin produced by Aspergillus flavus and Aspergillus parasiticus (Hugo Vanden Bossche, D.W.R. Mackenzie and G. Cauwenbergh. Aspergillus and Aspergillosis, 1987).
Aflatoxin GM2
Aflatoxin GM2 is a minor mycotoxin produced by Aspergillus flavus and Aspergillus parasiticus (Hugo Vanden Bossche, D.W.R. Mackenzie and G. Cauwenbergh. Aspergillus and Aspergillosis, 1987).
5,6,7,8-Tetrahydroxy-3',4'-dimethoxyflavone
5,6,7,8-Tetrahydroxy-3,4-dimethoxyflavone is found in citrus. 5,6,7,8-Tetrahydroxy-3,4-dimethoxyflavone is isolated from Seville orange (Citrus aurantium). Isolated from Seville orange (Citrus aurantium). 5,6,7,8-Tetrahydroxy-3,4-dimethoxyflavone is found in citrus.
N1-(2-Hydroxyethyl)flurazepam
N1-(2-Hydroxyethyl)flurazepam is a metabolite of flurazepam. Flurazepam (marketed under the brand names Dalmane and Dalmadorm) is a drug which is a benzodiazepine derivative. It possesses anxiolytic, anticonvulsant, sedative and skeletal muscle relaxant properties. It produces a metabolite with a very long half-life (40–250 hours), which may stay in the bloodstream for up to four days. http://www. non-benzodiazepines. org. uk/equivalents. html Flurazepam is therefore unsuitable as a sleeping medication for some individuals due to next day sedation. (Wikipedia)
6-(5-carboxy-2,3-dihydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid
6-(5-carboxy-2,3-dihydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 3,4,5-trihydroxybenzoic acid. It is generated by UDP-glucuronosyltransferase 1-1 (P22309) enzyme via an aromatic-OH-glucuronidation reaction. This aromatic-OH-glucuronidation occurs in humans.
Hydroxydehydro Nifedipine Carboxylate
Raclopride
Cyathusal B
An organic heterotricyclic compound that is 1H,6H-pyrano[4,3-c]isochromene-7-carbaldehyde substituted by hydroxy groups at positions 6, 9 and 10, methoxy group at position 8, oxo group at position 1 and a propenyl group at position 3. It is isolated from the fermented mushroom Cyathus stercoreus and exhibits radical scavenging activities.
Leucanthogenin
Leucanthogenin is a natural product found in Sideritis leucantha with data available.
Quercetagetin 3,4-dimethyl ether
Gossypetin 3,7-dimethyl ether
Gossypetin 3,8-dimethyl ether
7,8,3,4-Trihydroxy-3,5-dimethoxyflavone
Ganhuangenin
Viscidulin III is a compound isolated from the roots of Scutellaria planipes (L.)[1]. Viscidulin III can inhibit the proliferation of HL-60 (IC50= 17.4μM). Viscidulin III is a potential natural tumor inhibitor[2]. Viscidulin III is a compound isolated from the roots of Scutellaria planipes (L.)[1]. Viscidulin III can inhibit the proliferation of HL-60 (IC50= 17.4μM). Viscidulin III is a potential natural tumor inhibitor[2].
Axillarin
A dimethoxyflavone that is the 3,6-dimethyl ether derivative of quercetagetin. 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,6-dimethoxy-4h-chromen-4-one, also known as 3,4,5,7-tetrahydroxy-3,6-dimethoxyflavone or 3,6-dimethoxyquercetagetin, is a member of the class of compounds known as 6-o-methylated flavonoids. 6-o-methylated flavonoids are flavonoids with methoxy groups attached to the C6 atom of the flavonoid backbone. Thus, 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,6-dimethoxy-4h-chromen-4-one is considered to be a flavonoid lipid molecule. 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,6-dimethoxy-4h-chromen-4-one is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,6-dimethoxy-4h-chromen-4-one can be found in german camomile, which makes 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,6-dimethoxy-4h-chromen-4-one a potential biomarker for the consumption of this food product.
Syringetin
Syringetin,?a flavonoid derivative, is associated with increased BMP-2 production. Syringetin stimulates osteoblast differentiation at various stages, from maturation to terminally differentiated osteoblasts[1]. Syringetin,?a flavonoid derivative, is associated with increased BMP-2 production. Syringetin stimulates osteoblast differentiation at various stages, from maturation to terminally differentiated osteoblasts[1].
Limocitrin
relative retention time with respect to 9-anthracene Carboxylic Acid is 1.074 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.078 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.072
3,5-dichloro-N-[(1-ethylpyrrolidin-2-yl)methyl]-2-hydroxy-6-methoxybenzamide
1,3,4,6-tetrahydroxy-5,8-dimethoxy-2-methylanthraquinone|5,8-Di-Me ether-1,3,4,5,6,8-Hexahydroxy-2-methylanthraquinone
1,3,4,5-tetrahydroxy-7,8-dimethoxy-2-methylanthraquinone|5, 6-Di-Me ether-1, 2, 4, 5, 6, 8-Hexahydroxy-3-methylanthraquinone
18-Bromo-(9Z,17E)-octadeca-9,17-diene-5,7,15-triynoic acid
(13E,17E)-18-Bromo-13,17-octadecadiene-5,7-15-triynoic acid|18-Bromo-(13E,17E)-octadeca-9,17-diene-5,7,15-triynoic acid
(9E,15E)-form-18-Bromo-9,15-octadecadiene-5,7,17-triynoic acid
3,8-Dihydroxy-4,6-dimethoxy-9-oxo-9H-xanthene-1-carboxylic acid methyl ester
(-)-(3ar,3bt,5ac,5bt,10at,12ac)-dodecahydro-[1,2,5,6]tetrathiocino[3,4-a;8,7-a]dipyrrolizine|Cassiporin; 1alpha,1beta,2beta,2alpha-Bis-dithio-di-(7aalpha-pyrrolizidin)|cassipourine
(R)-5-hydroxy-2-methoxy-3-(2,3-dihydro-2-methoxycarbonyl-4-methyl-3-oxofuran-2-yl)-4H-1-benzopyran-4-one
(Z)-10-bromo-15-chloro-11,11-dimethyl-7-methylidenespiro[5.5]undec-3(15)-ene-4-one|dendroidone
1,3,5,8-Tetrahydroxy-6,7-dimethoxy-2-methyl-anthrachinon|1,3,5,8-tetrahydroxy-6,7-dimethoxy-2-methylanthraquinone|2,3-Di-Me ether-1,2,3,4,5,7-Hexahydroxy-6-methylanthraquinone
Aflatoxin G2a
1,2,3,6,8-pentahydroxy-7-(1-methoxyethyl)anthracene-9,10-dione
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6,8-dimethoxychromen-4-one
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,6-dimethoxychromen-4-one
Raclopride
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 C78272 - Agent Affecting Nervous System > C66883 - Dopamine Antagonist Raclopride is a dopamine D2/D3 receptor antagonist with potential antipsychotic effects. Raclopride binds to D2 and D3 receptors with Kis of 1.8 nM and 3.5 nM, respectively[1][2].
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6,8-dimethoxychromen-4-one
3,5-Pyridinedicarboxylic acid, 2-(hydroxymethyl)-6-methyl-4-(2-nitrophenyl)-, 5-methyl ester
Aflatoxin GM2
3,3-Bisjuglone
5,6,7,8-Tetrahydroxy-3',4'-dimethoxyflavone
18-bromo-13E,17E-octadecatrien-5,7,15-triynoic acid
4,4,5,5,6,6,6-heptafluoro-3,3-bis(trifluoromethyl)hex-1-ene
7-{[(4-METHOXYPHENYL)SULFONYL]AMINO}-1H-INDOLE-2-CARBOXYLICACID
Olsalazine sodium
D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D005765 - Gastrointestinal Agents D018501 - Antirheumatic Agents
(5R)-(+)-2,2,3-TRIMETHYL-5-BENZYL-4-IMIDAZOLIDINONE DICHLOROACETIC ACID
c-[4-(3,4-dichloro-benzyl)-morpholin-2-yl]-methylamine dihydrochloride
3,4-bis(2,4,5-trimethylthiophen-3-yl)furan-2,5-dione
1,1,1,2,2,4-Hexafluoro-3-[(1,3,3,4,4,4-hexafluoro-2-butanyl)oxy]b utane
(5S)-(-)-2,2,3-TRIMETHYL-5-BENZYL-4-IMIDAZOLIDINONE DICHLOROACETIC ACID
(6H-DIBENZ[C,E][1,2]OXAPHOSPHORIN-6-YLMETHYL)-P-OXIDE-BUTANEDIOIC ACID
2-CHLORO-2,2-DIFLUORO-1-(4-HYDROXYPIPERIDINO)-1-ETHANONE
4-CHLORO-2-[(PHENYLTHIO)METHYL]-5,6,7,8-TETRAHYDRO[1]BENZOTHIENO[2,3-D]PYRIMIDINE
4-(5-CHLORO-NAPHTHALENE-2-SULFONYL)-PIPERAZINE HYDROCHLORIDE
9-BROMO-1-BUTOXYBENZO[C][1,6]NAPHTHYRIDIN-6(5H)-ONE
4-(2-TRIFLUOROMETHOXY-BENZENESULFONYL)-PIPERAZINE HYDROCHLORIDE
5-(4-chlorobenzyloxycarbonyl)-4-(trifluoromethyl)pyrimidin-2-yl hydrazine
Ethyl 2-[Bis(2,2,2-Trifluoroethoxy)Phosphoryl]Propanoate
2-Oxo-2-phenylethyl 2-(4-(bromomethyl)phenyl)acetate
2-ETHOXY-5-[(PIPERIDINE-1-CARBONYL)-AMINO]-BENZENESULFONYL CHLORIDE
1-(5-chloro-2-nitrophenyl)-3,4-dihydro-6,7-dimethoxyisoquinoline
Pentamethonium bromide
C78272 - Agent Affecting Nervous System > C66880 - Anticholinergic Agent > C66886 - Nicotinic Antagonist
1-(4-((4-Bromophenyl)sulfonyl)piperazin-1-yl)ethanone
2,2-[1,2-Phenylenebis(oxy)]bis(1,3,2-benzodioxaborole)
1-[3,6-bis(4-chlorophenyl)-1H-1,2,4,5-tetrazin-2-yl]ethanone
Clodantoin
G - Genito urinary system and sex hormones > G01 - Gynecological antiinfectives and antiseptics > G01A - Antiinfectives and antiseptics, excl. combinations with corticosteroids C254 - Anti-Infective Agent > C514 - Antifungal Agent
ISOPROPYL 2-(4-CHLORO-6-PHENYLTHIENO[2,3-D]PYRIMIDIN-2-YL)ACETATE
6-Amino-8-chloro-4-[(3-chloro-4-fluorophenyl)amino]-3-quinolineca rbonitrile
2-[3-[[1-(4,5-dihydro-1,3-thiazol-2-yl)azetidin-3-yl]disulfanyl]azetidin-1-yl]-4,5-dihydro-1,3-thiazole
(2z)-2-Cyano-N-(2,2-Dichlorobiphenyl-4-Yl)-3-Hydroxybut-2-Enamide
Thiophene-2,5-disulfonic acid 2-amide-5-(4-methyl-benzylamide)
Raclopride C 11
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 C1446 - Radiopharmaceutical Compound > C2124 - Radioconjugate
aflatoxin B1 8,9-dihydrodiol
An aflatoxin B1 compound formed via enzymic epoxidation of aflatoxin B1 followed by non-enzymic hydrolysis.
4-(1H-benzimidazol-2-ylmethylsulfanyl)-2-methyl-[1]benzofuro[3,2-d]pyrimidine
5-bromo-N-[(1,2-dimethyl-5-indolyl)methyl]-2-furancarboxamide
Aflatoxin Q2a
D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D011042 - Poisons > D000348 - Aflatoxins
[(2R,3S,4R,5R)-5-(6-Amino-9H-purin-9-YL)-3,4-dihydroxytetrahydro-2-furanyl]methyl sulfamate
1-[(2-Nitrophenyl)sulfonyl]-1H-pyrrolo[3,2-B]pyridine-6-carboxamide
2-amino-N-(4-methyl-1,3-thiazol-2-yl)-5-[(4-methyl-4H-1,2,4-triazol-3-yl)sulfanyl]benzamide
(1s)-1(9-Deazahypoxanthin-9yl)1,4-dideoxy-1,4-imino-d-ribitol-5-phosphate
(3e)-5-Fluoro-1-[(6-Fluoro-4h-1,3-Benzodioxin-8-Yl)methyl]-1h-Indole-2,3-Dione 3-Oxime
Warfarin potassium
D006401 - Hematologic Agents > D000925 - Anticoagulants > D015110 - 4-Hydroxycoumarins D010575 - Pesticides > D012378 - Rodenticides D016573 - Agrochemicals
Eupatolitin
Eupatolitin is a tetrahydroxyflavone that is flavone substituted by hydroxy groups at positions 3, 5, 3 and 4 and methoxy groups at positions 6 and 7 respectively. It is a tetrahydroxyflavone, a dimethoxyflavone and a member of flavonols. It is functionally related to a flavone. Eupatolitin is a natural product found in Dicoma tomentosa, Haplopappus foliosus, and other organisms with data available. 6-methoxy-7-methylquercetin, also known as eupatoletin, is a member of the class of compounds known as flavonols. Flavonols are compounds that contain a flavone (2-phenyl-1-benzopyran-4-one) backbone carrying a hydroxyl group at the 3-position. Thus, 6-methoxy-7-methylquercetin is considered to be a flavonoid lipid molecule. 6-methoxy-7-methylquercetin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 6-methoxy-7-methylquercetin can be found in german camomile, which makes 6-methoxy-7-methylquercetin a potential biomarker for the consumption of this food product.
1-(2-carboxylatophenylamino)-1-deoxy-D-ribulose 5-phosphate(3-)
[5-(2,6-dioxo-3H-purin-9-yl)-3-hydroxyoxolan-2-yl]methyl phosphate
[(2R,3S,4R,5S)-3,4-dihydroxy-5-(5-hydroxybenzimidazol-1-yl)oxolan-2-yl]methyl dihydrogen phosphate
O3-[2-(trifluoromethyl)benzoyl]-4-chloro-1-methyl-1H-pyrazole-3-carbohydroximamide
4-[(E)-[5-chloro-3-methyl-1-(4-methylphenyl)pyrazol-4-yl]methylideneamino]-3-methyl-1H-1,2,4-triazole-5-thione
5-bromo-N-[2-(2-methyl-1-indolyl)ethyl]-2-furancarboxamide
4-[(2E)-2-[(E)-3-(2-nitrophenyl)prop-2-enylidene]hydrazinyl]benzenesulfonamide
7-chloro-5-(4-fluorophenyl)-4-(1-oxopropyl)-3,5-dihydro-1H-1,4-benzodiazepin-2-one
2-[(2-chlorophenyl)methoxy]-N-(4,5-dihydrothiazol-2-yl)benzamide
N-[2-(4-chlorophenyl)ethyl]-2-([1,2,4]triazolo[4,3-a]pyridin-3-ylthio)acetamide
N-(4,5-dithiophen-2-yl-2-thiazolyl)-2-methyl-1-cyclopropanecarboxamide
(6-chloroimidazo[1,2-a]pyridin-2-yl)methyl (E)-3-(3-chlorophenyl)prop-2-enoate
N-[(2,5-dichlorophenyl)methyl]-5-ethyl-1H-indole-2-carboxamide
(2S,3S,4R)-1-(4-fluorophenyl)sulfonyl-4-(hydroxymethyl)-3-phenyl-2-azetidinecarbonitrile
(2R,3S,4R)-1-(4-fluorophenyl)sulfonyl-4-(hydroxymethyl)-3-phenylazetidine-2-carbonitrile
(2R,3R,4S)-1-(4-fluorophenyl)sulfonyl-4-(hydroxymethyl)-3-phenyl-2-azetidinecarbonitrile
(2S,3R,4S)-1-(4-fluorophenyl)sulfonyl-4-(hydroxymethyl)-3-phenyl-2-azetidinecarbonitrile
(2R,3R,4R)-1-(4-fluorophenyl)sulfonyl-4-(hydroxymethyl)-3-phenyl-2-azetidinecarbonitrile
(2S,3R,4R)-1-(4-fluorophenyl)sulfonyl-4-(hydroxymethyl)-3-phenyl-2-azetidinecarbonitrile
(2S,3S,4S)-1-(4-fluorophenyl)sulfonyl-4-(hydroxymethyl)-3-phenyl-2-azetidinecarbonitrile
(2R,3S,4S)-1-(4-fluorophenyl)sulfonyl-4-(hydroxymethyl)-3-phenyl-2-azetidinecarbonitrile
Cephalexin(1-)
The anion resulting from the removal of a proton from the carboxylic acid group of cephalexin.
N-[(E)-[(Z)-2-bromo-3-phenylprop-2-enylidene]amino]-2,5-dimethylfuran-3-carboxamide
3-[(Z)-2-(5-chloro-2-hydroxyanilino)-1-nitroethenyl]-3H-2-benzofuran-1-one
(E)-3-(5-bromo-2-methoxyphenyl)-N-(pyridin-3-ylmethyl)prop-2-enamide
5,7-Dihydroxy-2-(1-hydroxy-3,5-dimethoxy-4-oxocyclohexa-2,5-dien-1-yl)chromen-4-one
2-hydroxy-3-[3-[(E)-4-hydroxy-3-methylbut-2-enyl]-4-sulooxyphenyl]propanoic acid
2,3-Dihydroxy-3-[3-(3-methylbut-2-enyl)-4-sulooxyphenyl]propanoic acid
Aflatoxin B1 diol
D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D011042 - Poisons > D000348 - Aflatoxins
N-(5-phosphonato-beta-D-ribosyl)anthranilate
An organophosphate oxoanion resulting from deprotonation of the phosphate and carboxy groups of N-(5-phospho-beta-D-ribosyl)anthranilic acid.
TuMP
A ribonucleoside monophosphate that is tubercidin with a phosphate group replacing the hydrogen on the 5-hydroxy group.
5,7,3,5-tetrahydroxy-3,4-dimethyoxyflavone
A tetrahydroxyflavone that is myricetin in which the hydroxy groups at positions 3 and 4 are replaced by methoxy groups. It has been isolated from Combretum quadrangulare.
(+)-taxifolin 3-O-acetate
An acetate ester obtained by formal condensation between the 3-hydroxy group of (+)-taxifolin and acetic acid.
IMP(2-)
A nucleoside 5-monophosphate(2-) that results from the removal of two protons from the phosphate group of IMP; major species at pH 7.3.
1-(2-carboxylatophenylamino)-1-deoxy-D-ribulose 5-phosphate(3-)
An organophosphate oxoanion resulting from the removal of a total of three protons from the phosphate and carboxy groups of 1-(2-carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate.
JNJ-42041935
JNJ-42041935 is a potent, competitive and selective inhibitor of prolyl hydroxylase PHD; inhibits PHD1, PHD2, and PHD3 with pKi values of 7.91±0.04, 7.29 ±0.05, and 7.65±0.09, respectively.
(1s,3r,5s,7s,8s)-10-bromo-8-chloro-7,11,11-trimethyl-3-(prop-1-en-2-yl)-4,6-dioxatricyclo[5.4.0.0¹,⁵]undec-9-ene
(2s,6'r)-3'-bromo-4-methyl-6'-(methylamino)-2'-azaspiro[furan-2,7'-tricyclo[6.3.1.0⁴,¹²]dodecane]-1'(11'),3',8'(12'),9'-tetraen-5-one
3-{[4-(3,8-dihydroxy-1,4-dioxonaphthalen-2-yl)but-3-en-1-yl]oxy}-3-oxopropanoic acid
(2s)-6-hydroxy-4,7'-dimethyl-6'-oxaspiro[1-benzofuran-2,2'-tricyclo[7.3.1.0⁵,¹³]tridecane]-1'(13'),4',7',9',11'-pentaene-3,3'-dione
(9e,17e)-18-bromooctadeca-9,17-dien-5,7,15-triynoic acid
2-(3,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-6-methoxychromen-4-one
(12r)-5-chloro-6,8-dihydroxy-12-methyl-11-oxatricyclo[12.4.0.0⁴,⁹]octadeca-1(18),4,6,8,14,16-hexaene-2,10-dione
2-(2,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-8-methoxychromen-4-one
3,7,8-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-methoxychromen-4-one
2,3,12,13-tetrathia-9,16-diazapentacyclo[12.6.0.0⁴,¹¹.0⁵,⁹.0¹⁶,²⁰]icosane
2-(2,6-dihydroxyphenyl)-5,6-dihydroxy-7,8-dimethoxychromen-4-one
2-(3,4-dihydroxyphenyl)-7,8-dihydroxy-3,6-dimethoxychromen-4-one
methyl 3,8-dihydroxy-4,6-dimethoxy-9-oxoxanthene-1-carboxylate
5,6,7-trihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3-methoxychromen-4-one
5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenoxy)-6-methoxychromen-4-one
6-(4,5-dihydroxy-2-phenylnaphthalen-1-yl)-4-hydroxypyran-2-one
5,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,6-dimethoxychromen-4-one
2-(2,3-dihydroxyphenyl)-n-hydroxy-n-[2-(3h-imidazol-4-yl)ethyl]-1,3-thiazole-4-carboxamide
3',5,5',7-tetrahydroxy-2',8-dimethoxyflavone
{"Ingredient_id": "HBIN007540","Ingredient_name": "3',5,5',7-tetrahydroxy-2',8-dimethoxyflavone","Alias": "NA","Ingredient_formula": "C17H14O8","Ingredient_Smile": "NA","Ingredient_weight": "346.293","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "NA","TCMSP_id": "NA","TCM_ID_id": "8270","PubChem_id": "NA","DrugBank_id": "NA"}
5,7,2,5-tetrahydroxy-8,6-dimethoxyflavone
{"Ingredient_id": "HBIN011163","Ingredient_name": "5,7,2,5-tetrahydroxy-8,6-dimethoxyflavone","Alias": "NA","Ingredient_formula": "C17H14O8","Ingredient_Smile": "NA","Ingredient_weight": "376.34","OB_score": "33.81582599","CAS_id": "NA","SymMap_id": "SMIT01177","TCMID_id": "NA","TCMSP_id": "MOL002909","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
5,7,3′,4′-Tetrahydroxy-6,5′-dimethoxyflavone
{"Ingredient_id": "HBIN011181","Ingredient_name": "5,7,3\u2032,4\u2032-Tetrahydroxy-6,5\u2032-dimethoxyflavone","Alias": "NA","Ingredient_formula": "C17H14O8","Ingredient_Smile": "COC1=CC(=CC(=C1O)O)C2=CC(=O)C3=C(C(=C(C=C3O2)O)OC)O","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "41033","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}