Exact Mass: 269.0358
Exact Mass Matches: 269.0358
Found 87 metabolites which its exact mass value is equals to given mass value 269.0358,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
N-Acetyl-L-glutamyl 5-phosphate
N-Acetyl-L-glutamyl 5-phosphate is an intermediate in urea cycle and metabolism of amino groups. The enzyme N-acetyl-gamma-glutamyl-phosphate reductase [EC:1.2.1.38] catalyzes the conversion of this metabolite into N-acetyl-L-glutamate 5-semialdehyde. This reaction is irreversible and occurs in the mitochondria. (BiGG database) [HMDB] N-Acetyl-L-glutamyl 5-phosphate is an intermediate in urea cycle and metabolism of amino groups. The enzyme N-acetyl-gamma-glutamyl-phosphate reductase [EC:1.2.1.38] catalyzes the conversion of this metabolite into N-acetyl-L-glutamate 5-semialdehyde. This reaction is irreversible and occurs in the mitochondria. (BiGG database).
(±)-Mephosfolan
(±)-Mephosfolan is an Agricultural insecticide with contact and stomach action, now supersede
Dansyl chloride
D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D003619 - Dansyl Compounds
3-(5-Acetamido-2-hydroxyphenyl)sulfanyl-2-oxopropanoic acid
3,4-DIHYDRO-2,2-DIOXO-7-METHOXYCARBONYL-1-METHYLBENZO[2,1-C]THIAZIN-4-ONE
(2E,4E)-1-PHENYL-4-(1,3,3-TRIMETHYL-1,3-DIHYDRO-2H-INDOL-2-YLIDENE)BUT-2-EN-1-ONE
(4-(4-Chlorophenoxy)phenyl)methanamine hydrochloride
4-(2,4,6-trifluorobenzoyl)-1H-pyrrole-2-carboxylic acid
2-((TERT-BUTYLDIMETHYLSILYLOXY)METHYL)-6-((TRIMETHYLSILYL)ETHYNYL)FURO[3,2-B]PYRIDINE
METHYL 2-AMINO-2-(4-(TRIFLUOROMETHYL)PHENYL)ACETATE HYDROCHLORIDE
(S)-3-AMINO-4-(2,4,5-TRIFLUOROPHENYL)BUTANOIC ACID HYDROCHLORIDE
N-[4-(2-Amino-4-thiazolyl)phenyl]methanesulfonamide
METHYL 7-CHLORO-2-METHYL-3-OXO-3,4-DIHYDRO-2H-1,4-BENZOXAZINE-2-CARBOXYLATE
Methanesulfonic acid, 1,1,1-trifluoro-, 4-[(1R)-1-aminoethyl]phenyl ester
3-[(4-chlorophenoxy)methyl]-4-ethyl-1H-1,2,4-triazole-5-thione
6-AMINO-2-([(2,3-DIFLUOROPHENYL)METHYL]SULFANYL)-3,4-DIHYDROPYRIMIDIN-4-ONE
Sulfasomizole
C254 - Anti-Infective Agent > C29739 - Sulfonamide Anti-Infective Agent
(R)-3-AMINO-4-(2,4,5-TRIFLUOROPHENYL)BUTANOIC ACID HYDROCHLORIDE
ethyl 2-(2,6-difluorophenyl)thiazole-4-carboxylate
4-(CHLOROMETHYL)-2-(3,4-DIMETHOXYPHENYL)-1,3-THIAZOLE HYDROCHLORIDE
Methyl 4-acetamido-5-chloro-2,3-dihydrobenzofuran-7-carboxylate
Ethyl 2-(2,4-difluorophenyl)thiazole-4-carboxylate
2-pyridin-2-yl-4-(trifluoromethyl)pyrimidine-5-carboxylic acid
1-(5-CHLORO-METHOXYPHENYL)-5-OXO-3-PYRROLIDINECARBOXYLIC ACID
1-(3-CHLORO-4-METHOXYPHENYL)-5-OXO-3-PYRROLIDINECARBOXYLIC ACID
3-(4-chlorophenyl)-4-(2-methoxyethyl)-1H-1,2,4-triazole-5-thione
Methyl 4-hydroxy-2-methyl-(2H)-1,2-benzothiazine-3-carboxylate-1,1-dioxide
(1E,4E)-1-(2,4-dichlorophenyl)-5-(dimethylamino)penta-1,4-dien-3-one
Emodin(1-)
A phenolate anion that is the conjugate base of emodin, obtained by deprotonation of the phenolic hydroxy group at position 2; major species at pH 7.3 (according to Marvin v 6.2.0.).
Genistein(1-)
An organic anion that is the conjugate base of genistein, obtained by selective deprotonation of the 7-hydroxy group.
Baicalein(1-)
A flavonoid oxoanion obtained by deprotonation of the hydroxy group at position 7 of baicalein. It is the major microspecies at pH 7.3 (according to Marvin v 6.2.0.).
Dansyl chloride
D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D003619 - Dansyl Compounds
phosphatidylethanolamine 37:0
A phosphatidylethanolamine in which the two acyl groups contain a total of 37 carbons and no double bonds.
phosphatidylethanolamine 19:1
A 1,2-diacyl-sn-glycero-3-phosphoethanolaminein which the two phosphatidyl acyl groups contain a total of 19 carbons and 1 double bond.
pelargonidin(1-)
An organic anion obtained by selective deprotonation of the 3- and 5-hydroxy groups of pelargonidin; major species at pH 7.3.
nataloe-emodin(1-)
A phenolate anion that is the conjugate base of nataloe-emodin, obtained by deprotonation of the phenolic hydroxy group at position 2. Major species at pH 7.3.
