C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@@H]3CN[C@H](CC4=CN(CC(O)=O)[N+](C)=C4)C3)=C(N2C1=O)C(O)=O

InChIKey=SCPWBKJMULYHAX-HQRPNPQYSA-O

C21H29N4O6S

465.54

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Aralkylamines Azepines Vinylogous thioesters Dicarboxylic acids and derivatives Tertiary carboxylic acid amides Pyrrolidines Pyrazoles Heteroaromatic compounds Thioenol ethers Amino acids Tertiary amines Azetidines Secondary alcohols Carboxylic acids Azacyclic compounds Dialkylamines Sulfenyl compounds Carbonyl compounds Organic oxides Hydrocarbon derivatives Organic cations

Aromatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Aralkylamine - Dicarboxylic acid or derivatives - Vinylogous thioester - Azole - Pyrazole - Heteroaromatic compound - Pyrrolidine - Pyrroline - Tertiary carboxylic acid amide - Amino acid or derivatives - Azetidine - Carboxamide group - Amino acid - Thioenolether - Secondary alcohol - Tertiary amine - Secondary amine - Sulfenyl compound - Azacycle - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Organic nitrogen compound - Hydrocarbon derivative - Alcohol - Organonitrogen compound - Amine - Carbonyl group - Organic oxide - Organooxygen compound - Organosulfur compound - Organic oxygen compound - Organic cation - 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