Exact Mass: 396.1838846
Exact Mass Matches: 396.1838846
Found 202 metabolites which its exact mass value is equals to given mass value 396.1838846,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
1-[2-Amino-6-(3,5-dimethoxyphenyl)pyrido[2,3-d]pyrimidin-7-yl]-3-tert-butylurea
C20H24N6O3 (396.19097939999995)
D004791 - Enzyme Inhibitors > D047428 - Protein Kinase Inhibitors
(10S,11R)-Pterosin C 4-glucoside
(10S,11R)-Pterosin C 4-glucoside is found in green vegetables. (10S,11R)-Pterosin C 4-glucoside is isolated from Pteridium aquilinum (bracken fern). Isolated from Pteridium aquilinum (bracken fern). (10S,11R)-Pterosin C 4-glucoside is found in green vegetables and root vegetables.
(S)-(E)-8-(3,6-Dimethyl-2-heptenyl)-4',5,7-trihydroxyflavanone
(S)-(E)-8-(3,6-Dimethyl-2-heptenyl)-4,5,7-trihydroxyflavanone is found in mushrooms. (S)-(E)-8-(3,6-Dimethyl-2-heptenyl)-4,5,7-trihydroxyflavanone is a constituent of Artocarpus communis (breadfruit). Constituent of Artocarpus communis (breadfruit). 8-(3,6-Dimethyl-2-heptenyl)-naringenin is found in mushrooms.
Pteroside P
Constituent of Pteridium aquilinum (bracken fern). Pteroside P is found in green vegetables and root vegetables. Pteroside P is found in green vegetables. Pteroside P is a constituent of Pteridium aquilinum (bracken fern).
4,5-Dihydroniveusin A
4,5-Dihydroniveusin A is found in fats and oils. 4,5-Dihydroniveusin A is a constituent of Helianthus annuus (sunflower). Constituent of Helianthus annuus (sunflower). 4,5-Dihydroniveusin A is found in sunflower and fats and oils.
(S)-(E)-2'-(3,6-Dimethyl-2-heptenyl)-3',4',7-trihydroxyflavanone
(S)-(E)-2-(3,6-Dimethyl-2-heptenyl)-3,4,7-trihydroxyflavanone is found in fruits. (S)-(E)-2-(3,6-Dimethyl-2-heptenyl)-3,4,7-trihydroxyflavanone is a constituent of Artocarpus communis (breadfruit). Constituent of Artocarpus communis (breadfruit). (S)-(E)-2-(3,6-Dimethyl-2-heptenyl)-3,4,7-trihydroxyflavanone is found in fruits.
(3'x,5'a,9'x,10'b)-O-(3-Hydroxy-6-oxo-7-drimen-11-yl)umbelliferone
(3x,5a,9x,10b)-O-(3-Hydroxy-6-oxo-7-drimen-11-yl)umbelliferone is found in herbs and spices. (3x,5a,9x,10b)-O-(3-Hydroxy-6-oxo-7-drimen-11-yl)umbelliferone is a constituent of Ferula galbaniflua (galbanum). Constituent of Ferula galbaniflua (galbanum). (3x,5a,9x,10b)-O-(3-Hydroxy-6-oxo-7-drimen-11-yl)umbelliferone is found in herbs and spices.
fluticasone 17beta-carboxylic acid
fluticasone 17beta-carboxylic acid is a metabolite of fluticasone propionate. Fluticasone propionate is a corticosteroid derived from fluticasone used to treat asthma and allergic rhinitis (hay fever). It is also used to treat eosinophilic esophagitis. (Wikipedia)
1-[2-Amino-6-(3,5-dimethoxyphenyl)pyrido[2,3-d]pyrimidin-7-yl]-3-tert-butylurea
C20H24N6O3 (396.19097939999995)
D004791 - Enzyme Inhibitors > D047428 - Protein Kinase Inhibitors
Lobetyolin
Lobetyolin
Unii-yjz71tro1X is a natural product found in Platycodon grandiflorus with data available. See also: Codonopsis pilosula root (part of). Lobetyolin, a bioactive compound, is derived from Codonopsis pilosula. Lobetyolin has anti-inflammatory, anti-oxidative and xanthine oxidase inhibiting activities. Lobetyolin also induces the apoptosis via the inhibition of ASCT2-mediated glutamine metabolism[1][2]. Lobetyolin is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Lobetyolin, a bioactive compound, is derived from Codonopsis pilosula. Lobetyolin has anti-inflammatory, anti-oxidative and xanthine oxidase inhibiting activities. Lobetyolin also induces the apoptosis via the inhibition of ASCT2-mediated glutamine metabolism[1][2]. Lobetyolin is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Lobetyolin, a bioactive compound, is derived from Codonopsis pilosula. Lobetyolin has anti-inflammatory, anti-oxidative and xanthine oxidase inhibiting activities. Lobetyolin also induces the apoptosis via the inhibition of ASCT2-mediated glutamine metabolism[1][2]. Lobetyolin is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
14,15β-dihydroxyklaineanone
14,15beta-Dihydroxyklaineanone is a natural product found in Eurycoma longifolia with data available.
Carmanin
Fukanemarin A
A hydroxycoumarin that is 4,7-dihydroxycoumarin substituted by a 1,2,6,10-tetramethyl-8-oxoundeca-2(E),5(E),9-trienyl moiety at position 3. Isolated from the roots of Ferula fukanensis, it exhibits inhibitory effects on the production of nitric oxide (NO).
(-)-2beta-{(E)-3-Hydroxy-3-methylbut-1-enyl}-2-deoxybruceol
4,5-Dihydroniveusin A
methyl 2-[1-(4-fluorobenzyl)-1h-indole-3-carboxamido]-3,3-dimethylbutanoate
(E)-3-(4-methoxyphenyl)-1-[2,4,6-trimethoxy-3-(3-methylbut-2-enyl)phenyl]prop-2-en-1-one
4-Hydroxycinnamoyl(E-)-15-Hydroxy-3,11(13)-eudesmadien-12-oic acid
2alpha-hydroxy-8beta-2,3,5-trihydroxyangeloyloxycostunolide
methyl ester of 8alpha-(2-hydroxymethyl-2-butenoyloxy)-1beta,6alpha-dihydroxy-15-oxo-11(13)eudesmen-12-oic acid
10-(beta-D-glucopyranosyloxy)tetradeca-2,8-diene-4,6-diyne-1,14-diol|cordifolioidyne B
1alpha,10beta,15-trihydroxy-3-oxo-8beta-O-methylbutanoyl-4,11(13)-germacradien, 6alpha,12-olide
2,3-dihydro-7-hydroxy-2R*,3R*-dimethyl-2-[4,8-dimethyl-4(Z),7-nonadien-6-onyl]furo[3,2-c]coumarin|fukanefuromarin D
1beta-methoxy-3alpha-hydroxy-3,10beta-4,5alpha-diepoxy-8beta-isobutyroyloxy-germacra-11(13)-en-6alpha,12-olide
2alpha-isovaleryloxy-3,8-dioxo-11-peroxy-4beta,5beta,7,14-bis-epoxybisabol-9E-ene
1beta-(E-cinnamoyloxy)-5alpha-hydroxypolygodial|1beta-E-cinnamoyl-5alpha-hydroxypolygodial
2,3-dihydro-7-hydroxy-2S*,3R*-dimethyl-2-[4,8-dimethyl-3(E),7-nonadien-6-onyl]-furo[3,2-c]coumarin|dihydro-7-hydroxy-2R*,3S*-dimethyl-2-[4,8-dimethyl-3(E),7-nonadien-6-onyl]furo[3,2-c]coumarin
(2Z,8Z,12R)-tetradecadiene-4,6-diyne-1,12,14-triol-1-O-beta-D-glucopyranoside
yadanziolide T
A quassinoid that is picras-3-ene substituted by hydroxy groups at positions 1, 11, 12, 15 and 21 and oxo groups at positions 2 and 16. Isolated from the ethanol extract of the stem of Brucea mollis, it exhibits cytotoxic activity.
6beta,11alpha,16beta,17-tetrahydroxy-6,7-seco-6,20-epoxy-1alpha,7-olide-ent-kaur-15-one|jianshirubesin C
(1S,5R,8S,10R,11S,12S,13S)-5,8,11,12-diepoxy-10,13-dihydroxy-1-isopropenyl-8-methyl-3,6-dioxocyclotetradecan-12-carboxylate|gyrosanin A
3alpha,6beta,11beta,16beta-tetrahydroxy-6alpha,20-epoxy-6,7-seco-ent-kaur-15-one-1alpha,7-olide|sculponin P
2alpha,3alpha,10alpha,13alpha,16alpha,17-hexahydroxy-9alpha-methyl-15-oxo-20-nor-kauran-19-oic acid (19,10)-lactone|2??,3??,10??,13??,16??,17-Hexahydroxy-9??-methyl-15-oxo-20-nor-kauran-19-oic acid (19,10)-lactone
(6E,12E)-tetradecadiene-8,10-diyne-1,14-diol-3-O-beta-D-glucopyranoside
2(R),3(R)-pterosin L 3-O-alpha-L-arabinopyranoside
(1S,5S,6R,7R,8R,9S,10S,11R)-8,9-epoxy-1-hydroxy-2-oxo-5-angeloxyxanthan-6,12-olide
7-[6-(beta-carboxyethyl)-4-isopropenyl-2,6-dimethylcyclohex-2-enylmethyloxy]coumarin
2alpha,9alpha-dihydroxydivaricatolide-8-O-angelate
Tox21_303565
C20H29ClN2O4 (396.18157440000004)
Quinine hydrochloride dihydrate (Qualaquin) is an orally active and can be used in anti-malarial studies. Quinine hydrochloride dihydrate is a potassium channel inhibitor that inhibits WT mouse Slo3 (KCa5.1) channel currents evoked by voltage pulses to +100?mV with an IC50 of 169 μM[1][2].
14,15 β-Dihydroxyklaineanone
14,15beta-Dihydroxyklaineanone is a natural product found in Eurycoma longifolia with data available.
Quinine hydrochloride dihydrate
C20H29ClN2O4 (396.18157440000004)
Quinine hydrochloride dihydrate (Qualaquin) is an orally active and can be used in anti-malarial studies. Quinine hydrochloride dihydrate is a potassium channel inhibitor that inhibits WT mouse Slo3 (KCa5.1) channel currents evoked by voltage pulses to +100?mV with an IC50 of 169 μM[1][2].
(E)-3-(4-methoxyphenyl)-1-[2,4,6-trimethoxy-3-(3-methylbut-2-enyl)phenyl]prop-2-en-1-one
2-[6-(3,4-dihydroxy-2-methylidenebutanoyl)oxy-4-ethenyl-2-hydroxy-3-(3-hydroxyprop-1-en-2-yl)-4-methylcyclohexyl]prop-2-enoic acid
(2S,3S,9R,12R,13R,14S,15R,16R,17S)-3,12,13,15,16-pentahydroxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadec-5-ene-4,11-dione
(E)-3-(4-methoxyphenyl)-1-[2,4,6-trimethoxy-3-(3-methylbut-2-enyl)phenyl]prop-2-en-1-one [IIN-based: Match]
(E)-3-(4-methoxyphenyl)-1-[2,4,6-trimethoxy-3-(3-methylbut-2-enyl)phenyl]prop-2-en-1-one [IIN-based on: CCMSLIB00000846372]
(2S,3S,9R,12R,13R,14S,15R,16R,17S)-3,12,13,15,16-pentahydroxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.0²,?.0¹³,¹?]heptadec-5-ene-4,11-dione
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Pteroside P
(10S,11R)-Pterosin C 4-glucoside
(3'x,5'a,9'x,10'b)-O-(3-Hydroxy-6-oxo-7-drimen-11-yl)umbelliferone
(S)-(E)-2'-(3,6-Dimethyl-2-heptenyl)-3',4',7-trihydroxyflavanone
(S)-(E)-8-(3,6-Dimethyl-2-heptenyl)-4',5,7-trihydroxyflavanone
2.4.4.6-Tetramethylether-3-prenylchalcone
Methyl 3-(1-Tritylimidazol-4-yl) Propionate
C26H24N2O2 (396.18376839999996)
4-(1-TRITYL-1H-IMIDAZOL-4-YL)-BUTYRIC ACID
C26H24N2O2 (396.18376839999996)
1,3-Phenylenebis(2,2-propanediyl-4,1-phenylene) dicyanate
C26H24N2O2 (396.18376839999996)
N,N-Bis[[4-(2-propen-1-yloxy)phenyl]methylene]-1,4-benzenediamine
C26H24N2O2 (396.18376839999996)
Succinylcholine Chloride Dihydrate
D018373 - Peripheral Nervous System Agents > D009465 - Neuromuscular Agents > D009466 - Neuromuscular Blocking Agents
Thiourea, N-[2-(1H-benzimidazol-2-yl)ethyl]-N-cyclohexyl-N-(4-fluorophenyl)- (9CI)
5-Amino-5-deoxy-2,3-O-(1-methylethylidene)-N-(phenylmethyl)adenosine
C20H24N6O3 (396.19097939999995)
4-[[6-[(1-Oxo-2-propenyl)oxy]hexyl]oxy]benzoic acid 4-ethylphenyl ester
bis[tris(hydroxyethyl)ammonium] sulphate
C12H32N2O10S (396.17775720000003)
PF-04620110
PF-04620110 is a potent, selective and orally bioavailable diglyceride acyltransferase-1 (DGAT-1) inhibitor with an IC50 of 19 nM[1].
(6S,8S,9R,10S,11S,13S,14S,16R,17R)-6,9-difluoro-11,17-dihydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthrene-17-carboxylic acid
(2r)-3-(Phosphonooxy)propane-1,2-Diyl Diheptanoate
C17H33O8P (396.19129480000004)
(6e,11e)-Heptadeca-6,11-Diene-9,9-Diylbis(Phosphonic Acid)
3,12,13,15,16-Pentahydroxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-5-ene-4,11-dione
2-[(4Z,12E)-1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
Fukanefuromarin A
A furanocoumarin that is 2,3-dihydrofuro[3,2-c]coumarin substituted by a hydroxy group at position 7, methyl groups at positions 2 and 3 (relatively cis configuration) and a 4,8-dimethyl-4(E),7-nonadien-6-onyl moiety at position 2. Isolated from the roots of Ferula fukanensis, it inhibits production of nitric oxide (NO).
Fukanefuromarin C
A furanocoumarin that is 2,3-dihydrofuro[3,2-c]coumarin substituted by a hydroxy group at position 7, methyl groups at positions 2 and 3 (relatively cis configuration) and a 4,8-dimethyl-4(Z),7-nonadien-6-onyl moiety at position 2. Isolated from the roots of Ferula fukanensis, it inhibits production of nitric oxide (NO).
Fukanefuromarin B
A furanocoumarin that is 2,3-dihydrofuro[3,2-c]coumarin substituted by a hydroxy group at position 7, methyl groups at positions 2 and 3 (relatively trans configuration) and a 4,8-dimethyl-4(E),7-nonadien-6-onyl moiety at position 2. Isolated from the roots of Ferula fukanensis, it inhibits production of nitric oxide (NO).
(2R*,3R*)-2,3-dihydro-7-hydroxy-2,3-dimethyl-2-[4,8-dimethyl-3(E)-7-nonadien-6-onyl]furo[3,2-c]coumarin
A furanocoumarin that is 2,3-dihydrofuro[3,2-c]coumarin substituted by a hydroxy group at position 7, methyl groups at positions 2 and 3 (relatively trans configuration) and a 4,8-dimethyl-3(E)-7-nonadien-6-onyl moiety at position 2. Isolated from the roots of Ferula fukanensis, it exhibits inhibitory effect on the production of nitric oxide (NO).
Fukanefuromarin D
A furanocoumarin that is 2,3-dihydrofuro[3,2-c]coumarin substituted by a hydroxy group at position 7, methyl groups at positions 2 and 3 (relatively trans configuration) and a 4,8-dimethyl-4(Z),7-nonadien-6-onyl moiety at position 2. Isolated from the roots of Ferula fukanensis, it inhibits production of nitric oxide (NO).
(2S*,3R*)-2,3-dihydro-7-hydroxy-2,3-dimethyl-2-[4,8-dimethyl-3(E),7-nonadien-6-onyl]-furo[3,2-c]coumarin
A furanocoumarin that is 2,3-dihydrofuro[3,2-c]coumarin substituted by a hydroxy group at position 7, methyl groups at positions 2 and 3 (relatively cis configuration) and a 4,8-dimethyl-3(E),7-nonadien-6-onyl moiety at position 2. Isolated from the roots of Ferula fukanensis and Ferula ferulioides, it exhibits inhibitory activity against production of nitric oxide (NO).
2-(1-ethyl-4-oxo-3-furo[3,4]pyrrolo[3,5-c][1,2,4]triazinyl)-N-[4-(2-furanyl)butan-2-yl]propanamide
N-[(2S)-1-(1H-benzimidazol-2-ylamino)-3-methyl-1-oxobutan-2-yl]-3,5-dimethoxybenzamide
3-(2-methylpropyl)-6-[4-[3-(trifluoromethyl)phenyl]-1-piperazinyl]-1H-pyrimidine-2,4-dione
2-[(2S,3R,6S)-3-[[anilino(oxo)methyl]amino]-2-(hydroxymethyl)-3,6-dihydro-2H-pyran-6-yl]-N-(2-pyridinylmethyl)acetamide
2-[(2S,3S,6R)-3-[[anilino(oxo)methyl]amino]-2-(hydroxymethyl)-3,6-dihydro-2H-pyran-6-yl]-N-(2-pyridinylmethyl)acetamide
2-[(2S,3S,6S)-3-[[anilino(oxo)methyl]amino]-2-(hydroxymethyl)-3,6-dihydro-2H-pyran-6-yl]-N-(2-pyridinylmethyl)acetamide
2-[(2R,3S,6S)-3-[[anilino(oxo)methyl]amino]-2-(hydroxymethyl)-3,6-dihydro-2H-pyran-6-yl]-N-(2-pyridinylmethyl)acetamide
2-[(2R,3S,6R)-3-[[anilino(oxo)methyl]amino]-2-(hydroxymethyl)-3,6-dihydro-2H-pyran-6-yl]-N-(2-pyridinylmethyl)acetamide
2-[(2R,3R,6S)-3-[[anilino(oxo)methyl]amino]-2-(hydroxymethyl)-3,6-dihydro-2H-pyran-6-yl]-N-(2-pyridinylmethyl)acetamide
2-[(2R,3R,6R)-3-[[anilino(oxo)methyl]amino]-2-(hydroxymethyl)-3,6-dihydro-2H-pyran-6-yl]-N-(2-pyridinylmethyl)acetamide
(S)-[(2S,4S,5R)-5-Ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methanol;dihydrate;hydrochloride
C20H29ClN2O4 (396.18157440000004)
(2R,3R,4S,5S,6R)-2-[(4Z,6R,7R,12E)-1,6-dihydroxytetradeca-4,12-dien-8,10-diyn-7-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
3-O,5-O-diethyl 4-O-[2-oxo-2-(propan-2-ylamino)ethyl] 2,6-dimethyl-3,4-dihydropyridine-3,4,5-tricarboxylate
(2S,3S,9R,12R,13R,14S,15R,16R,17S)-3,12,13,15,16-pentahydroxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-5-ene-4,11-dione
(1-Acetyloxy-3-phosphonooxypropan-2-yl) dodecanoate
C17H33O8P (396.19129480000004)
2-[6-(3,4-Dihydroxy-2-methylidenebutanoyl)oxy-4-ethenyl-2-hydroxy-3-(3-hydroxyprop-1-en-2-yl)-4-methylcyclohexyl]prop-2-enoic acid
(1-Hexanoyloxy-3-phosphonooxypropan-2-yl) octanoate
C17H33O8P (396.19129480000004)
(1-Pentanoyloxy-3-phosphonooxypropan-2-yl) nonanoate
C17H33O8P (396.19129480000004)
(1-Phosphonooxy-3-propanoyloxypropan-2-yl) undecanoate
C17H33O8P (396.19129480000004)
(1-Butanoyloxy-3-phosphonooxypropan-2-yl) decanoate
C17H33O8P (396.19129480000004)
(3x,5a,9x,10b)-O-(3-Hydroxy-6-oxo-7-drimen-11-yl)umbelliferone
(S)-(E)-8-(3,6-Dimethyl-2-heptenyl)-4,5,7-trihydroxyflavanone
(S)-(E)-2-(3,6-Dimethyl-2-heptenyl)-3,4,7-trihydroxyflavanone
phosphatidic acid 14:0
C17H33O8P (396.19129480000004)
A phosphatidic acid in which the two acyl groups contain a total of 14 carbons and no double bonds.