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

InChIKey=NCTYNCNVCOORFO-YVJUOBEVSA-N

C21H31ClN4O5S

487.01

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

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

Aromatic heteropolycyclic compounds

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