C[C@H](O)[C@@H]1[C@@H]2CC(SCC[NH+]=CN)=C(N2C1=O)C([O-])=O

InChIKey=ZSKVGTPCRGIANV-ACLDMZEESA-N

C12H17N3O4S

299.35

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

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

Aliphatic heteropolycyclic compounds

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