Exact Mass: 462.1304
Exact Mass Matches: 462.1304
Found 95 metabolites which its exact mass value is equals to given mass value 462.1304
,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
Artomunoxanthentrione epoxide
Artomunoxanthentrione epoxide is found in fruits. Artomunoxanthentrione epoxide is isolated from the root bark of Artocarpus communis (breadfruit). Isolated from the root bark of Artocarpus communis (breadfruit). Artomunoxanthentrione epoxide is found in fruits.
2-(4-hydroxyphenyl)ethyl 4-hydroxy-2-(4-hydroxybenzyl)-3-(4-hydroxyphenyl)-5-oxo-2,5-dihydrofuran-2-carboxylate|rac-secoretipolide E
vanillic acid 1-O-[beta-D-apiofuranosyl-(1?6)-beta-D-glucopyranoside]ester
6-O-beta-apiofuranosyl-[5-O-(3-methoxy,4-hydroxybenzoyl)oxy]-alpha/beta-glucopyranoside
1-Hydroxy-3-methyl-4-(2-hydroxy-3-acetyl-4,6-dimethoxyphenyl)-8-methoxyanthracene-9,10-dione
beta-D-glucopyranosyl 4-O-beta-D-glucopyranosylbenzoate
2-hydroxy-4,5-methylenedioxyphenol-1-O-alpha-L-rhamnopyranosyl-(1->6)-beta-D-glucopyranoside
C19H26O13_beta-D-Fructofuranosyl 6-O-(4-hydroxybenzoyl)-alpha-D-glucopyranoside
[(2R,3S,4S,5R,6R)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxybenzoate
[(2R,3S,4S,5R,6R)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxybenzoate_major
Cys Cys His Thr
Cys Cys Thr His
Cys His Cys Thr
Cys His Thr Cys
Cys Thr Cys His
Cys Thr His Cys
His Cys Cys Thr
His Cys Thr Cys
His Thr Cys Cys
Thr Cys Cys His
Thr Cys His Cys
Thr His Cys Cys
Artomunoxanthentrione epoxide
Benzamide,N,N-(9,10-dihydro-4-hydroxy-9,10-dioxo-1,5-anthracenediyl)bis-
1,3,5-Tri-O-benzoyl-α-D-ribofuranose
1,3,5-Tri-O-benzoyl-a-D-ribofuranose is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].
5-(2,4-BIS(BENZYLOXY)-5-CHLOROPHENYL)-N-ETHYLISOXAZOLE-3-CARBOXAMIDE
(3r,4r)-1-{6-[3-(Methylsulfonyl)phenyl]pyrimidin-4-Yl}-4-(2,4,5-Trifluorophenyl)piperidin-3-Amine
N-monoacetylchitobiose-6-phosphate
A disaccharide phosphate that is N-monoacetylchitobiose substituted at position 6 by a phospho group.
2-[[2-(1-Adamantyl)-2-oxoethyl]thio]-6-amino-4-(4-chlorophenyl)pyridine-3,5-dicarbonitrile
4-methyl-N-(3-methylphenyl)-N-[2-oxo-2-[(2-oxo-3-indolyl)hydrazo]ethyl]benzenesulfonamide
(E)-2-cyano-N-(5-methyl-2-phenylpyrazol-3-yl)-3-[5-[3-(trifluoromethyl)phenyl]furan-2-yl]prop-2-enamide
(2R,3R)-8-bromo-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-2-[[methyl(3-pyridinylmethyl)amino]methyl]-3,4-dihydro-2H-pyrido[2,3-b][1,5]oxazocin-6-one
(2R,3R)-8-bromo-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-2-[[methyl(3-pyridinylmethyl)amino]methyl]-3,4-dihydro-2H-pyrido[2,3-b][1,5]oxazocin-6-one
4-[(4,5-Diphenyl-2-oxazolyl)thio]-1-(4-nitrophenyl)butane-1,3-diol
4-methoxyphenyl 3-O-(beta-D-glucopyranuronosyl)-beta-D-galactopyranoside
ethyl 2-[[(Z)-2-cyano-3-(3,4-dimethoxyphenyl)prop-2-enoyl]amino]-4-phenylthiophene-3-carboxylate
Meclizine hydrochloride
D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D018680 - Cholinergic Antagonists D018377 - Neurotransmitter Agents > D018494 - Histamine Agents > D006633 - Histamine Antagonists C308 - Immunotherapeutic Agent > C29578 - Histamine-1 Receptor Antagonist D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents C78272 - Agent Affecting Nervous System > C267 - Antiemetic Agent D005765 - Gastrointestinal Agents > D000932 - Antiemetics D002491 - Central Nervous System Agents D018926 - Anti-Allergic Agents
JW 642
JW 642 is a potent inhibitor of monoacylglycerol lipase (MAGL) that displays IC50 values of 7.6, 14, and 3.7 nM for inhibition of MAGL in mouse, rat, and human brain membranes, respectively. IC50 value: 7.6/14/3.7 nM(mouse/rat/human MAGL) [1] Target: MAGL inhibitor JW 642 is selective for MAGL, requiring much higher concentrations to effectively inhibit fatty acid amide hydrolase activity (IC50s = 31, 14, and 20.6 μM for mouse, rat, and human brain membranes, respectively).