CC(O)[C@@H]1[C@H]2CC(SCCNC(C)=O)=C(N2C1=O)C(O)=O

InChIKey=VUDXUIMGYZQRKK-JYXTUMRVSA-N

C13H18N2O5S

314.36

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Azepines Vinylogous thioesters Acetamides Tertiary carboxylic acid amides Thioenol ethers Tertiary amines Amino acids Azetidines Secondary carboxylic acid amides Secondary alcohols Carboxylic acids Monocarboxylic acids and derivatives Sulfenyl compounds Azacyclic 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 - Pyrroline - Tertiary carboxylic acid amide - Acetamide - Amino acid or derivatives - Azetidine - Carboxamide group - Amino acid - Secondary alcohol - Secondary carboxylic acid amide - Tertiary amine - Thioenolether - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Azacycle - Sulfenyl compound - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Amine - Hydrocarbon derivative - Alcohol - Organic oxygen compound - 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