C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@@H]3CN[C@H](CS[C@H]4CCNC4)C3)=C(N2C1=O)C(O)=O

InChIKey=VDNGSDZLPNQEPF-UBRSESRLSA-N

C19H29N3O4S2

427.58

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

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

Aliphatic heteropolycyclic compounds

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