Exact Mass: 286.0621346
Exact Mass Matches: 286.0621346
Found 89 metabolites which its exact mass value is equals to given mass value 286.0621346,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
Glycineamideribotide
Glycinamidoribotide conversion to N-formylglycinamide ribonucleotide is the third reaction of the de novo purine biosynthesis, a reaction catalyzed by the enzyme Glycinamide ribonucleotide transformylase (EC 2.1.2.2), with concomitant conversion of 10-formyltetrahydrofolate to tetrahydrofolate. (PMID: 9143358). Glycineamideribotide formation is stimulated by Luteinizing hormone (LH) and Chorionic gonadotropin (HCG) via activation of Glc-6-P-dehydrogenase (EC 1.1.1.49). (PMID: 4366083) [HMDB] Glycinamidoribotide conversion to N-formylglycinamide ribonucleotide is the third reaction of the de novo purine biosynthesis, a reaction catalyzed by the enzyme Glycinamide ribonucleotide transformylase (EC 2.1.2.2), with concomitant conversion of 10-formyltetrahydrofolate to tetrahydrofolate. (PMID: 9143358). Glycineamideribotide formation is stimulated by Luteinizing hormone (LH) and Chorionic gonadotropin (HCG) via activation of Glc-6-P-dehydrogenase (EC 1.1.1.49). (PMID: 4366083).
Uralenneoside
Uralenneoside is found in herbs and spices. Uralenneoside is a constituent of the leaves of Glycyrrhiza uralensis (Chinese licorice). Constituent of the leaves of Glycyrrhiza uralensis (Chinese licorice). Uralenneoside is found in herbs and spices.
3'-Methoxyfukiic acid
3-Methoxyfukiic acid is found in green vegetables. 3-Methoxyfukiic acid is isolated from Petasites japonicus (sweet coltsfoot
Diphenol glucuronide
Diphenol glucuronide belongs to the family of Glucuronides. These are compounds comprising the glucuronic acid linked to another substance via a glycosidic bond.
Fenclorac
C14H16Cl2O2 (286.05272959999996)
C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic C471 - Enzyme Inhibitor > C1323 - Cyclooxygenase Inhibitor
Imirestat
C471 - Enzyme Inhibitor > C72880 - Aldose Reductase Inhibitor
2-methoxy-6-[5-(prop-1-yn-1-yl)-2-thienyl]-hexa-3,5-diyn-1-yl acetate
3-alpha-L-arabinopyranosyloxy-4-hydroxybenzoic acid
2,2-dimethyl-8-(phenylthio)-4H-benzo[d][1,3]dioxin-4-one
Olprinone hydrochloride
D004791 - Enzyme Inhibitors > D010726 - Phosphodiesterase Inhibitors > D058987 - Phosphodiesterase 3 Inhibitors D020011 - Protective Agents > D002316 - Cardiotonic Agents D002317 - Cardiovascular Agents
2-FLUORO-2-METHANESULFONYLOXYMETHYL-MALONIC ACID DIETHYL ESTER
1-methyl-5-phenoxy-3-(trifluoromethyl)pyrazole-4-carboxylic acid
C12H9F3N2O3 (286.05652399999997)
(4-METHOXY-BENZYL)-PYRIDIN-3-YL-AMINE DIHYDROCHLORIDE
C13H16Cl2N2O (286.06396259999997)
5-METHYL-2-(4-TRIFLUOROMETHOXYPHENYL)-3H-IMIDAZOLE-4-CARBOXYLIC ACID
C12H9F3N2O3 (286.05652399999997)
2-[[2-(benzylsulfonylamino)acetyl]amino]acetate
C11H14N2O5S (286.06233940000004)
3-[(4-acetamidophenyl)sulfonylamino]propanoic acid
C11H14N2O5S (286.06233940000004)
4-[(1-phenyl-1H-tetrazol-5-yl)thio]pyrocatechol
C13H10N4O2S (286.05244400000004)
4-(BENZYLOXY)BENZENE-1,2-DIAMINE DIHYDROCHLORIDE
C13H16Cl2N2O (286.06396259999997)
Sodium carbonate decahydrate
C78275 - Agent Affecting Blood or Body Fluid > C29730 - Electrolyte Replacement Agent
3-Cyano-N,N-dimethyl-6-nitro-4-oxo-1,4-dihydro-8-quinolinecarboxa mide
4-methoxy-6-methyl-5-nitro-2-(trifluoromethyl)quinoline
C12H9F3N2O3 (286.05652399999997)
(4,6-DIMETHYL-PYRIMIDIN-2-YLSULFANYL)-PHENYL-ACETICACID
C11H14N2O5S (286.06233940000004)
3-(BENZO[D]THIAZOL-2-YL)-4,5,6,7-TETRAHYDROBENZO[B]THIOPHEN-2-AMINE
1-(4-methoxyphenyl)-5-(trifluoromethyl)pyrazole-4-carboxylic acid
C12H9F3N2O3 (286.05652399999997)
5-(AMINOSULFONYL)-2-MORPHOLIN-4-YLBENZOIC ACID
C11H14N2O5S (286.06233940000004)
4-(furan-2-ylmethyl)-2,3-dihydro-1H-quinoxaline
C13H16Cl2N2O (286.06396259999997)
3-Cyclopentyl-2-(3,4-dichlorophenyl)propanoic acid
C14H16Cl2O2 (286.05272959999996)
2-[3,5-bis(trifluoromethyl)phenyl]-N-hydroxyethanimidamide
6-(4-fluorophenyl)-4-methylsulfanylpyrido[3,2-d]pyrimidin-2-amine
C14H11FN4S (286.06884180000003)
Glycine,N-[(4-methylphenyl)sulfonyl]glycyl-
C11H14N2O5S (286.06233940000004)
4(1H)-Quinazolinone,3-(3-fluoro-4-methylphenyl)-2,3-dihydro-2-thioxo-
2-(3,5-Dichloro-4-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
2-[2-fluoro-4-[(2-methylpropan-2-yl)oxycarbonyl]phenyl]sulfanylacetic acid
N-[(E)-(4-hydroxy-3-nitrophenyl)methylidene]pyridine-4-carbohydrazide
3-[(3-Fluorophenyl)methylthio]-6-(2-furanyl)pyridazine
3-deoxy-3-fluoro-D-erythro-alpha-L-manno-non-2-ulopyranosonic acid
Fenclorac
C14H16Cl2O2 (286.05272959999996)
C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic C471 - Enzyme Inhibitor > C1323 - Cyclooxygenase Inhibitor
2-hydroxy-5-[(2R,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxybenzoic acid
(2-Methylbenzimidazol-1-yl)-[(5-nitro-2-thienyl)methylene]amine
C13H10N4O2S (286.05244400000004)
N-[(2-nitrophenyl)-oxomethyl]-2-pyridinecarbohydrazide
4-Methoxy-1,3-dimethyl-6-thiophen-2-yl-8-cyclohepta[c]furanone
2-cyano-3-oxo-N-[4-(trifluoromethoxy)phenyl]butanamide
C12H9F3N2O3 (286.05652399999997)
4-oxo-2-(trifluoromethyl)-1H-quinazoline-6-carboxylic acid ethyl ester
C12H9F3N2O3 (286.05652399999997)
hydrogen ({[(2R)-1-(6-amino-9H-purin-9-yl)propan-2-yl]oxy}methyl)phosphonate
3,4,5-Trihydroxy-6-(2-hydroxyphenoxy)oxane-2-carboxylic acid
4-Acetoxymethyl-6-chloromethyl-2,5-dimethoxy-2,4,6-cycloheptatrien-1-one
cytosylglucuronate
A carbohydrate acid derivative anion that is the conjugate base of cytosylglucuronic acid, obtained by deprotonation of the carboxy group.
2,3-dihydroxybenzoic acid 3-O-beta-D-xyloside
A monohydroxybenzoic acid that is 2-hydroxybenzoic acid in which the hydrogen at position 3 is replaced by a beta-D-xylosyloxy group.
tenofovir(1-)
A phosphorus oxoanion resulting from the removal of one proton from the phosphonic acid group of tenofovir. The major microspecies at pH 7.3.
catechol beta-D-glucuronide
A glucosiduronic acid that is beta-D-glucuronic acid in which the anomeric hydroxyl hydrogen has been replaced by a 2-hydroxyphenyl group.