C[C@@H](O)[C@@H]1C2C(C)C(SC3CCC(NC3)\C=C\N3CC=CC3)=C(N2C1=O)C(O)=O

InChIKey=JSPOMPRLJUCXRD-XUAYVZPQSA-N

C21H29N3O4S

419.54

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

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

Aliphatic heteropolycyclic compounds

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