Chemical Formula: C4H6N2O2S
Chemical Formula C4H6N2O2S
Found 17 metabolite its formula value is C4H6N2O2S
(Z)-2-CHLORO-2-BUTENE
An imidothiocarbamic ester that is (2Z)-prop-2-enoic acid with a carbamimidoylsulfanyl group at position 3.
(4S)-2-amino-4,5-dihydro-1,3-thiazole-4-carboxylic acid
2-Amino-4,5-dihydro-1,3-thiazol-3-ium-4-carboxylate
(4R)-2-amino-4,5-dihydro-1,3-thiazol-3-ium-4-carboxylate
(4S)-2-amino-4,5-dihydro-1,3-thiazol-3-ium-4-carboxylate
2-Amino-delta(2)-thiazoline-4-carboxylic acid
A 1,3-thiazole that is 4,5-dihydro-1,3-thiazole which is substituted at positions 2 and 4 by an amino and a carboxy group, respectively.
D-2-amino-Delta(2)-thiazoline-4-carboxylic acid
A 2-amino-Delta(2)-thiazoline-4-carboxylic acid that has S configuration.
D-2-amino-Delta(2)-thiazoline-4-carboxylic acid zwitterion
A 2-amino-Delta(2)-thiazoline-4-carboxylic acid zwitterion that has S-configuration. The major species at pH 7.3.
L-2-amino-Delta(2)-thiazoline-4-carboxylic acid
A 2-amino-Delta(2)-thiazoline-4-carboxylic acid that has R configuration.
2-amino-Delta(2)-thiazoline-4-carboxylic acid zwitterion
An amino acid zwitterion obtained from 2-amino-Delta(2)-thiazoline-4-carboxylic acid by the transfer of a proton from the carboxy group to the thiazoline nitrogen. The major species at pH 7.3.
L-2-amino-Delta(2)-thiazoline-4-carboxylic acid zwitterion
A 2-amino-Delta(2)-thiazoline-4-carboxylic acid zwitterion that has R-configuration. The major species at pH 7.3.
