C[C@@H](O)[C@@H]1[C@@H]2[C@@H](C)C(S[C@H]3CNC(=S)C3)=C(N2C1=O)C(O)=O

InChIKey=SXTYKFYKGOOCOC-RXMKQEINSA-N

C14H18N2O4S2

342.43

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Azepines Vinylogous thioesters Thiolactams Tertiary carboxylic acid amides Pyrrolidines Thioenol ethers Secondary alcohols Azetidines Sulfenyl compounds Azacyclic compounds Monocarboxylic acids and derivatives Carboxylic acids Carbonyl compounds Hydrocarbon derivatives Organic oxides Organonitrogen compounds Thiocarbonyl compounds

Aliphatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Vinylogous thioester - Pyrrolidine - Pyrroline - Thiolactam - Tertiary carboxylic acid amide - Azetidine - Carboxamide group - Secondary alcohol - Thioenolether - Sulfenyl compound - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Azacycle - Alcohol - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Thiocarbonyl group - Aliphatic 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