[Cl-].C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@@H]3CN[C@H](CC4=CN5CCC[N+]5=C4)C3)=C(N2C1=O)C(O)=O

InChIKey=XSBHCCZHCOSESU-POZMKREASA-N

C21H29ClN4O4S

469.0

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

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

Aromatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid or derivatives - Pyrroline carboxylic acid - Azepine - Aralkylamine - Vinylogous thioester - Pyrroline - Tertiary carboxylic acid amide - Heteroaromatic compound - Azole - Pyrazole - Pyrrolidine - Carboxamide group - Thioenolether - Azetidine - Tertiary amine - 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 - Organic oxygen compound - Amine - Organic nitrogen compound - Organic chloride salt - Carbonyl group - Alcohol - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic salt - Organic zwitterion - Organic oxide - 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