C[C@@H](O)C1[C@H]2[C@@H](C)C(SC3CN(C3)C3=NCCSC3(C)C)=C(N2C1=O)C(O)=O

InChIKey=LUEJVSNSYAAAEO-TWHNVLESSA-N

C19H27N3O4S2

425.56

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Azepines Vinylogous thioesters Imidolactams Tertiary carboxylic acid amides Thioenol ethers Azetidines Secondary alcohols Monocarboxylic acids and derivatives Azacyclic compounds Dialkylthioethers Carboxylic acids Carboximidamides Carboxamidines Propargyl-type 1,3-dipolar organic compounds Sulfenyl compounds Carbonyl compounds Hydrocarbon derivatives Amines Organic oxides

Aliphatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Vinylogous thioester - Imidolactam - Pyrroline - Tertiary carboxylic acid amide - Azetidine - Carboxamide group - Secondary alcohol - Thioenolether - Thioether - Amidine - Dialkylthioether - Propargyl-type 1,3-dipolar organic compound - Azacycle - Sulfenyl compound - Carboximidamide - Organic 1,3-dipolar compound - Carboxylic acid amidine - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Carboxylic acid - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Alcohol - Organic oxygen compound - Amine - Organosulfur compound - Organic oxide - Hydrocarbon derivative - 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