C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@H]3C[C@@H]4N(C3)C(C)(C)N(CC=C)C4=O)=C(N2C1=O)C(O)=O

InChIKey=XSLPXGNNHWDEMD-PEZGRIKUSA-N

C21H29N3O5S

435.54

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Azepines Vinylogous thioesters Imidazolidinones N-alkylpyrrolidines Tertiary carboxylic acid amides Thioenol ethers Azetidines Secondary alcohols Carboxylic acids Sulfenyl compounds Azacyclic compounds Monocarboxylic acids and derivatives Hydrocarbon derivatives Carbonyl compounds Amines Organic oxides

Aliphatic heteropolycyclic compounds

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