CC(O)C1C2C(C)C(S[C@@H]3CN(C(=O)C3)C3=CC(F)=NC=C3)=C(N2C1=O)C(O)=O

InChIKey=NTSJUSCTJQVGGY-XBINOLHCSA-N

C19H20FN3O5S

421.44

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids 2-halopyridines Azepines Vinylogous thioesters Aryl fluorides Pyrrolidine-2-ones Tertiary carboxylic acid amides Heteroaromatic compounds Thioenol ethers Secondary alcohols Azetidines Carboxylic acids Sulfenyl compounds Azacyclic compounds Monocarboxylic acids and derivatives Organofluorides Carbonyl compounds Organonitrogen compounds Hydrocarbon derivatives Organic oxides

Aromatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - 2-halopyridine - Azepine - Aryl fluoride - Aryl halide - Pyridine - Pyrrolidone - Vinylogous thioester - 2-pyrrolidone - Heteroaromatic compound - Pyrrolidine - Tertiary carboxylic acid amide - Pyrroline - Secondary alcohol - Thioenolether - Azetidine - Carboxamide group - Sulfenyl compound - Azacycle - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organosulfur compound - Hydrocarbon derivative - Organic oxide - Alcohol - Organic oxygen compound - 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