C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(SCCN)=C(N2C1=O)C(O)=O

InChIKey=LJSXRKPRIVMADK-WCTZXXKLSA-N

C12H18N2O4S

286.35

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

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

Aliphatic heteropolycyclic compounds

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