C[C@@H](O)[C@@H]1[C@@H]2[C@@H](C)C(SCC(=N)N3CCN(C)C(=O)C3)=C(N2C1=O)C(O)=O

InChIKey=QKAUXZKEESWQJH-RQSQLSILSA-N

C17H24N4O5S

396.46

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

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

Aliphatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - N-alkylpiperazine - N-methylpiperazine - 1,4-diazinane - Piperazine - Vinylogous thioester - Pyrroline - Tertiary carboxylic acid amide - Azetidine - Carboxamide group - Secondary alcohol - Thioenolether - Azacycle - Amidine - Carboximidamide - Sulfenyl compound - Carboxylic acid amidine - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Carboxylic acid - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Carbonyl group - Alcohol - Organic oxygen compound - Organooxygen compound - Organosulfur compound - Organic nitrogen 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