[I-].C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@@H]3CN[C@@H](C3)C3CC[N+](C)(C)CC3)=C(N2C1=O)C(O)=O

InChIKey=QGUTXBKBLVYSJD-RVXXKJSYSA-N

C21H34IN3O4S

551.48

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Azepines Vinylogous thioesters Piperidines Tetraalkylammonium salts Tertiary carboxylic acid amides Pyrrolidines Thioenol ethers Azetidines Secondary alcohols Amino acids Monocarboxylic acids and derivatives Azacyclic compounds Dialkylamines Carboxylic acids Sulfenyl compounds Carbonyl compounds Hydrocarbon derivatives Organic iodide salts Organic oxides Organic zwitterions

Aliphatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Vinylogous thioester - Piperidine - Quaternary ammonium salt - Tetraalkylammonium salt - Pyrroline - Tertiary carboxylic acid amide - Pyrrolidine - Carboxamide group - Thioenolether - Azetidine - Amino acid - Secondary alcohol - Amino acid or derivatives - Azacycle - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Monocarboxylic acid or derivatives - Sulfenyl compound - Secondary amine - Organonitrogen compound - Organic oxygen compound - Amine - Organic nitrogen compound - Alcohol - Carbonyl group - Organooxygen compound - Organosulfur compound - Organic iodide salt - Organic salt - Organic zwitterion - Organic oxide - 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