C[C@H](OS([O-])(=O)=O)[C@H]1[C@H]2CC(SCCNC(C)=O)=C(N2C1=O)C([O-])=O

InChIKey=HZYSJDYRQDXUAB-IONOHQLYSA-L

C13H16N2O8S2

392.4

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Azepines Vinylogous thioesters Sulfuric acid monoesters Alkyl sulfates Acetamides Tertiary carboxylic acid amides Thioenol ethers Secondary carboxylic acid amides Azetidines Carboxylic acid salts Carboxylic acids Azacyclic compounds Sulfenyl compounds Monocarboxylic acids and derivatives Carbonyl compounds Organonitrogen compounds Hydrocarbon derivatives Organic oxides Organic anions

Aliphatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Vinylogous thioester - Sulfuric acid ester - Alkyl sulfate - Sulfuric acid monoester - Sulfate-ester - Organic sulfuric acid or derivatives - Acetamide - Pyrroline - Tertiary carboxylic acid amide - Azetidine - Carboxamide group - Carboxylic acid salt - Secondary carboxylic acid amide - Thioenolether - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Azacycle - Sulfenyl compound - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organic anion - 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