C[C@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@@H]3CN[C@@H](C3)\C=C3\CCNC3=O)=C(N2C1=O)C(O)=O

InChIKey=FXKYKPSYANEVOX-ZXSPJXFOSA-N

C19H25N3O5S

407.49

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Azepines Vinylogous thioesters Pyrrolidine-2-ones Tertiary carboxylic acid amides Thioenol ethers Amino acids Azetidines Secondary carboxylic acid amides Secondary alcohols Dialkylamines Carboxylic acids Monocarboxylic acids and derivatives Sulfenyl compounds Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides

Aliphatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Pyrrolidone - 2-pyrrolidone - Vinylogous thioester - Tertiary carboxylic acid amide - Pyrrolidine - Pyrroline - Carboxamide group - Thioenolether - Secondary carboxylic acid amide - Secondary alcohol - Amino acid - Azetidine - Amino acid or derivatives - Sulfenyl compound - Secondary amine - Azacycle - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Secondary aliphatic amine - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Carbonyl group - Alcohol - Organic oxygen compound - Amine - Organic oxide - Organic nitrogen compound - 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