CC(O)C1C2C(C)C(S[C@@H]3CN(C(=O)O3)C3=CC(F)=NC=C3)=C(N2C1=O)C(O)=O

InChIKey=OHHRLSBYWOGJFZ-YOPQSGLCSA-N

C18H18FN3O6S

423.42

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

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

Aromatic heteropolycyclic compounds

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