C[C@@H](O)[C@@H]1[C@H]2CC(S[C@@H]3CN[C@H](CC4CCNC4=O)C3)=C(N2C1=O)C(O)=O

InChIKey=CYPKKVDRZFINGE-ARDDLRKFSA-N

C18H25N3O5S

395.47

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Azepines Vinylogous thioesters Pyrrolidine-2-ones Tertiary carboxylic acid amides Thioenol ethers Secondary carboxylic acid amides Secondary alcohols Amino acids Azetidines Sulfenyl compounds Monocarboxylic acids and derivatives Azacyclic compounds Dialkylamines Carboxylic acids Carbonyl compounds Hydrocarbon derivatives Organic oxides Organopnictogen compounds

Aliphatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Pyrrolidone - 2-pyrrolidone - Vinylogous thioester - Pyrrolidine - Pyrroline - Tertiary carboxylic acid amide - Carboxamide group - Azetidine - Amino acid or derivatives - Amino acid - Secondary alcohol - Secondary carboxylic acid amide - Thioenolether - Carboxylic acid - Azacycle - Carboxylic acid derivative - Sulfenyl compound - Secondary amine - Monocarboxylic acid or derivatives - Secondary aliphatic amine - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Alcohol - Carbonyl group - Organic oxygen compound - Organopnictogen compound - Amine - Organic nitrogen compound - Organic oxide - 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