CCOC(=O)C1CSC(N1)[C@@H]1C[C@@H](CN1)SC1=C(N2C(C([C@@H](C)O)C2=O)[C@H]1C)C(O)=O

InChIKey=VEENMRVKQRJYLC-JMGLMJQISA-N

C20H29N3O6S2

471.59

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

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

Aliphatic heteropolycyclic compounds

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