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

InChIKey=ZMLFVSLVHOLPIZ-HQRPNPQYSA-O

C21H30N5O5S

464.56

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

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

Aromatic heteropolycyclic compounds

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