C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@@H]3CN[C@@H](C3)C3CC(CO)=NO3)=C(N2C1=O)C(O)=O

InChIKey=YXQTZIACDXXVLI-KIDJYRSWSA-N

C18H25N3O6S

411.47

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Azepines Vinylogous thioesters Tertiary carboxylic acid amides Isoxazolines Pyrrolidines Azetidines Thioenol ethers Amino acids Oxime ethers Secondary alcohols Sulfenyl compounds Monocarboxylic acids and derivatives Carboxylic acids Oxacyclic compounds Dialkylamines Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Primary alcohols

Aliphatic heteropolycyclic compounds

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