CC1(C)S[C@@H]2[C@@H](NC(=O)[C@@H](C([O-])=O)C3=CSC=C3)C(=O)N2[C@@H]1C([O-])=O

InChIKey=OHKOGUYZJXTSFX-APOZVJGGSA-L

C15H14N2O6S2

382.41

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Penams

Penicillins

N-acyl-alpha amino acids and derivatives 1,3-dicarbonyl compounds Dicarboxylic acids and derivatives Thiophenes Thiazolidines Tertiary carboxylic acid amides Heteroaromatic compounds Amino acids Azetidines Carboxylic acid salts Tertiary amines Secondary carboxylic acid amides Dialkylthioethers Carboxylic acids Thiohemiaminal derivatives Azacyclic compounds Hydrocarbon derivatives Organic oxides Organic anions

Aromatic heteropolycyclic compounds

Penicillin - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - Dicarboxylic acid or derivatives - 1,3-dicarbonyl compound - Tertiary carboxylic acid amide - Heteroaromatic compound - Thiazolidine - Thiophene - Amino acid or derivatives - Azetidine - Carboxamide group - Carboxylic acid salt - Amino acid - Secondary carboxylic acid amide - Tertiary amine - Carboxylic acid - Carboxylic acid derivative - Azacycle - Thioether - Hemithioaminal - Dialkylthioether - Carbonyl group - Amine - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic anion - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as penicillins. These are organic compounds containing the penicillin core structure, which is structurally characterized by a penam ring bearing two methyl groups at position 2, and an amide group at position 6 [starting from the sulfur atom at position 1].

Not available