C[C@@H](O)C1C2[C@@H](C)C(SC3CN(C3)C3=NC(CN)=CO3)=C(N2C1=O)C(O)=O

InChIKey=ZYKNCWYTTPBKRV-JWWSKVQJSA-N

C17H22N4O5S

394.45

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Dialkylarylamines Pyrroline carboxylic acids 2,4-disubstituted oxazoles Aralkylamines Azepines Vinylogous thioesters Heteroaromatic compounds Tertiary carboxylic acid amides Thioenol ethers Azetidines Amino acids Secondary alcohols Oxacyclic compounds Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Sulfenyl compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Dialkylarylamine - 2,4-disubstituted 1,3-oxazole - Azepine - Aralkylamine - Vinylogous thioester - Azole - Oxazole - Heteroaromatic compound - Pyrroline - Tertiary carboxylic acid amide - Carboxamide group - Amino acid or derivatives - Amino acid - Azetidine - Secondary alcohol - Thioenolether - Carboxylic acid - Oxacycle - Azacycle - Sulfenyl compound - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic nitrogen compound - Primary aliphatic amine - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organosulfur compound - Primary amine - Hydrocarbon derivative - Organic oxide - Amine - Organic oxygen compound - Alcohol - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as thienamycins. These are beta-lactam antibiotics that differ from penicillins in having the thiazolidine sulfur atom replaced by carbon, the sulfur then becoming the first atom in the side chain.

Not available