C[C@@H](O)[C@@H]1C2[C@@H](C)C(S[C@H]3C[C@@H](CSCCC(N)=O)N(C3)C(C)=N)=C(N2C1=O)C(O)=O

InChIKey=NOAGGAWLWVIWBL-OMUXTXSMSA-N

C20H30N4O5S2

470.6

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 Secondary alcohols Primary carboxylic acid amides Azetidines Sulfenyl compounds Azacyclic compounds Monocarboxylic acids and derivatives Dialkylthioethers Carboxylic acids Carboximidamides Carboxamidines Organic oxides Carbonyl compounds Hydrocarbon derivatives

Aliphatic heteropolycyclic compounds

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