C[C@@H](O)C1[C@H]2[C@@H](C)C(SC3CN(C3)C3=NCCCCS3)=C(N2C1=O)C(O)=O

InChIKey=ACCGHBQBOVJXAS-TWHNVLESSA-N

C18H25N3O4S2

411.54

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

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

Aliphatic heteropolycyclic compounds

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