CC(O)[C@@H]1[C@H]2[C@@H](C)C(SC3C[C@@H]4N(C3)[C@](C)(NC4=O)C=C)=C(N2C1=O)C(O)=O

InChIKey=PMEKMGUXBBYYSX-MBZCDCNQSA-N

C19H25N3O5S

407.49

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Azepines Vinylogous thioesters Imidazolidinones N-alkylpyrrolidines Tertiary carboxylic acid amides Thioenol ethers Azetidines Secondary carboxylic acid amides Secondary alcohols Carboxylic acids Azacyclic compounds Monocarboxylic acids and derivatives Sulfenyl compounds Hydrocarbon derivatives Carbonyl compounds Amines Organic oxides

Aliphatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Imidazolidinone - Vinylogous thioester - N-alkylpyrrolidine - Imidazolidine - Pyrrolidine - Pyrroline - Tertiary carboxylic acid amide - Secondary alcohol - Thioenolether - Secondary carboxylic acid amide - Azetidine - Carboxamide group - Sulfenyl compound - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Carboxylic acid - Organic nitrogen compound - Alcohol - Organic oxide - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organosulfur compound - Organic oxygen compound - Amine - Hydrocarbon derivative - 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