Chemical Formula: C7H11N3O2S
Chemical Formula C7H11N3O2S
Found 17 metabolite its formula value is C7H11N3O2S
1-methyl-5-thiol-L-histidine|5-Mercapto-1-methylhistidine
1-methyl-5-thiol-L-histidine|5-Mercapto-1-methylhistidine
2-AMINO-N-(PYRIDIN-4-YL)ETHANESULFONAMIDEHYDROCHLORIDE
2-AMINO-N-(PYRIDIN-4-YL)ETHANESULFONAMIDEHYDROCHLORIDE
[1-(2-cyanoethylsulfanyl)ethylideneamino] N-methylcarbamate
[1-(2-cyanoethylsulfanyl)ethylideneamino] N-methylcarbamate
ethyl 5-amino-3-methylthio-1H pyrazole-4-carboxylate
ethyl 5-amino-3-methylthio-1H pyrazole-4-carboxylate
[(5-ISOPROPYL-4H-1,2,4-TRIAZOL-3-YL)THIO]ACETIC ACID
[(5-ISOPROPYL-4H-1,2,4-TRIAZOL-3-YL)THIO]ACETIC ACID
1H-Imidazole-4-carboxylicacid,5-amino-2-(methylthio)-,ethylester(9CI)
1H-Imidazole-4-carboxylicacid,5-amino-2-(methylthio)-,ethylester(9CI)
2-Hydrazino-4-methyl-thiazole-5-carboxylic acid ethyl ester
2-Hydrazino-4-methyl-thiazole-5-carboxylic acid ethyl ester
Ovothiol A
Ovothiol A
A L-histidine derivative that is L-histidine substituted at positions N3 and C5 on the imidazole ring by methyl and mercapto groups respectively.
(2S)-2-azaniumyl-3-(1-methyl-4-sulfanyl-1H-imidazol-5-yl)propanoate
(2S)-2-azaniumyl-3-(1-methyl-4-sulfanyl-1H-imidazol-5-yl)propanoate
ovothiol A zwitterion
ovothiol A zwitterion
An L-alpha-amino acid zwitterion formed from ovothiol A by transfer of a proton from the carboxy to the amino group; major species at pH 7.3.
2-amino-3-(3-methyl-5-sulfanylimidazol-4-yl)propanoic acid
2-amino-3-(3-methyl-5-sulfanylimidazol-4-yl)propanoic acid
