[K+].C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(SC3CN(C3)[C@@H](C)C3=CC=CC=C3)=C(N2C1=O)C([O-])=O

InChIKey=XKUJDXABQDKATQ-ZTTIKTJFSA-M

C21H25KN2O4S

440.6

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Aralkylamines Azepines Vinylogous thioesters Benzene and substituted derivatives Tertiary carboxylic acid amides Trialkylamines Amino acids Thioenol ethers Azetidines Secondary alcohols Carboxylic acid salts Azacyclic compounds Sulfenyl compounds Carboxylic acids Monocarboxylic acids and derivatives Carbonyl compounds Hydrocarbon derivatives Organic oxides Organic potassium salts Organic zwitterions

Aromatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Aralkylamine - Monocyclic benzene moiety - Vinylogous thioester - Benzenoid - Pyrroline - Tertiary carboxylic acid amide - Amino acid or derivatives - Azetidine - Carboxamide group - Carboxylic acid salt - Amino acid - Secondary alcohol - Tertiary amine - Thioenolether - Tertiary aliphatic amine - Azacycle - Sulfenyl compound - Organic alkali metal salt - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic salt - Organonitrogen compound - Organooxygen compound - Alcohol - Organosulfur compound - Amine - Organic oxygen compound - Organic nitrogen compound - Organic oxide - Carbonyl group - Organic potassium salt - Hydrocarbon derivative - Organic zwitterion - Aromatic 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