C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(SC3CN(C)C(=O)C3)=C(N2C1=O)C(=O)OCOC(=O)C(C)(C)C

InChIKey=OIEGRCACJAQSLV-CNJGIHLQSA-N

C21H30N2O7S

454.54

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Acylals Azepines Vinylogous thioesters Dicarboxylic acids and derivatives N-alkylpyrrolidines Pyrrolidine-2-ones Enoate esters Tertiary carboxylic acid amides Thioenol ethers Azetidines Secondary alcohols Acetals Azacyclic compounds Sulfenyl compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Organopnictogen compounds

Aliphatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Acylal - Dicarboxylic acid or derivatives - Pyrrolidone - 2-pyrrolidone - Vinylogous thioester - N-alkylpyrrolidine - Pyrrolidine - Alpha,beta-unsaturated carboxylic ester - Pyrroline - Tertiary carboxylic acid amide - Enoate ester - Thioenolether - Secondary alcohol - Azetidine - Carboxamide group - Carboxylic acid ester - Sulfenyl compound - Azacycle - Acetal - Carboxylic acid derivative - Organic oxygen compound - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Carbonyl group - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Alcohol - 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