C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@@H]3CN[C@H](CSCCC(=O)N(CCO)CC(=O)N4CCCCC4)C3)=C(N2C1=O)C(O)=O

InChIKey=PTMUDTMOVDPRJC-NEQPJDIOSA-N

C27H42N4O7S2

598.77

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives N-acylpiperidines Pyrroline carboxylic acids Azepines Vinylogous thioesters Tertiary carboxylic acid amides Pyrrolidines Thioenol ethers Amino acids Azetidines Secondary alcohols Dialkylthioethers Dialkylamines Carboxylic acids Alkanolamines Sulfenyl compounds Monocarboxylic acids and derivatives Azacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides Primary alcohols

Aliphatic heteropolycyclic compounds

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