C[C@@H]1[C@@H]2[C@H](C(=O)N2C(C(O)=O)=C1S[C@@H]1CN[C@@H](C1)C(=O)N(C)C)C(C)(C)O

InChIKey=IUGBPEMORZZIBY-YBXAARCKSA-N

C18H27N3O5S

397.49

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

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

Aliphatic heteropolycyclic compounds

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