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=UDKDFEKRCWMDNF-HQRPNPQYSA-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 Sulfenyl compounds Monocarboxylic acids and derivatives Carbonyl compounds Aromatic alcohols Hydrocarbon derivatives Organic oxides Primary alcohols Organic cations

Aromatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid or derivatives - Pyrroline carboxylic acid - Azepine - Aralkylamine - Vinylogous thioester - Pyrroline - Heteroaromatic compound - Azole - Tertiary carboxylic acid amide - Pyrazole - Pyrrolidine - Thioenolether - Carboxamide group - Tertiary amine - Azetidine - Secondary alcohol - Amino acid - 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 - Carbonyl group - Alcohol - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Primary alcohol - Organic oxide - Aromatic alcohol - 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