C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(SC3CN4N=C[N+](C)=C4C3)=C(N2C1=O)C([O-])=O

InChIKey=IDZQHHSNDXIHML-IECIGANESA-N

C16H20N4O4S

364.42

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Azepines Vinylogous thioesters Triazoles Tertiary carboxylic acid amides Heteroaromatic compounds Thioenol ethers Azetidines Carboxylic acid salts Secondary alcohols Monocarboxylic acids and derivatives Azacyclic compounds Carboxylic acids Sulfenyl compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides Organic salts Organic zwitterions Organonitrogen compounds

Aromatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Vinylogous thioester - Azole - Heteroaromatic compound - 1,2,4-triazole - Tertiary carboxylic acid amide - Pyrroline - Azetidine - Carboxamide group - Carboxylic acid salt - Thioenolether - Secondary alcohol - Azacycle - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Sulfenyl compound - Organic oxygen compound - Organic salt - Organic nitrogen compound - Alcohol - Carbonyl group - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic zwitterion - Organic oxide - Aromatic 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