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

InChIKey=LDGZGOSYQJVSJB-PNQSVWQFSA-N

C20H21FN2O5S

420.46

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

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

Aromatic heteropolycyclic compounds

Thienamycin - 1-phenylpyrrolidine - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Halobenzene - Fluorobenzene - Monocyclic benzene moiety - Aryl halide - Aryl fluoride - 2-pyrrolidone - Pyrrolidone - Benzenoid - Vinylogous thioester - Pyrrolidine - Tertiary carboxylic acid amide - Pyrrole - Pyrroline - Azetidine - Carboxamide group - Thioenolether - Secondary alcohol - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Carboxylic acid - Sulfenyl compound - Organic oxygen compound - Organohalogen compound - Organic nitrogen compound - Carbonyl group - Organofluoride - Alcohol - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Organosulfur 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