CC1=C(C=CO1)C(=O)N[C@H]1[C@@H]2SC(C)(C)[C@H](N2C1=O)C([O-])=O

InChIKey=PDAOKCWWODOTAA-LNLATYFQSA-M

C14H15N2O5S

323.34

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Penams

Penicillins

N-acyl-alpha amino acids and derivatives Furan-3-carboxylic acid and derivatives Thiazolidines Tertiary carboxylic acid amides Heteroaromatic compounds Amino acids Tertiary amines Secondary carboxylic acid amides Azetidines Carboxylic acid salts Thiohemiaminal derivatives Azacyclic compounds Oxacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Dialkylthioethers Organic oxides Carbonyl compounds Hydrocarbon derivatives Organic anions

Aromatic heteropolycyclic compounds

Penicillin - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - Furoic acid or derivatives - Furan-3-carboxylic acid or derivatives - Furan - Tertiary carboxylic acid amide - Heteroaromatic compound - Thiazolidine - Amino acid or derivatives - Azetidine - Carboxamide group - Carboxylic acid salt - Amino acid - Secondary carboxylic acid amide - Tertiary amine - Azacycle - Dialkylthioether - Hemithioaminal - Thioether - Oxacycle - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Amine - Carbonyl group - Organic nitrogen compound - 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