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

InChIKey=WVDZWGKSZKENLR-JEFOHARNSA-O

C21H31N4O5S

451.56

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 Alkanolamines Sulfenyl compounds Monocarboxylic acids and derivatives Carbonyl compounds Hydrocarbon derivatives Organic oxides Primary alcohols Organic cations

Aromatic heteropolycyclic compounds

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