C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@@H]3CN[C@@H](C3)C3CCCN(C)CC3)=C(N2C1=O)C(O)=O

InChIKey=WCTHCCOTCBEFIT-SDPACTRSSA-N

C21H33N3O4S

423.57

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

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

Aliphatic heteropolycyclic compounds

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