C[C@@H](O)C1C2[C@@H](C)C(SC3CN(C3)C3=NC(CO)=CO3)=C(N2C1=O)C(O)=O

InChIKey=RMPWCPFHPBBSSX-JWWSKVQJSA-N

C17H21N3O6S

395.43

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Dialkylarylamines 2,4-disubstituted oxazoles Azepines Vinylogous thioesters Tertiary carboxylic acid amides Heteroaromatic compounds Thioenol ethers Secondary alcohols Azetidines Oxacyclic compounds Carboxylic acids Sulfenyl compounds Azacyclic compounds Monocarboxylic acids and derivatives Primary alcohols Carbonyl compounds Aromatic alcohols Hydrocarbon derivatives Organic oxides

Aromatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Dialkylarylamine - Azepine - 2,4-disubstituted 1,3-oxazole - Vinylogous thioester - Heteroaromatic compound - Azole - Oxazole - Pyrroline - Tertiary carboxylic acid amide - Thioenolether - Secondary alcohol - Azetidine - Carboxamide group - Sulfenyl compound - Oxacycle - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Azacycle - Organic oxygen compound - Aromatic alcohol - Alcohol - Carbonyl group - Hydrocarbon derivative - Amine - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxide - Primary alcohol - Organic nitrogen compound - 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