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

InChIKey=AAVQPKFARHMPBL-XMSOOASQSA-N

C29H39N3O8S

589.7

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Pyrrolidine carboxylic acids Azepines Vinylogous thioesters Tertiary carboxylic acid amides Carbamate esters Enoate esters Thioenol ethers Azetidines Secondary alcohols Sulfenyl compounds Azacyclic compounds Monocarboxylic acids and derivatives Organonitrogen compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides

Aliphatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrrolidine carboxylic acid - Pyrrolidine carboxylic acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Vinylogous thioester - Pyrrolidine - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carbamic acid ester - Tertiary carboxylic acid amide - Pyrroline - Azetidine - Carboxamide group - Carboxylic acid ester - Thioenolether - Secondary alcohol - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Azacycle - Sulfenyl compound - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxygen compound - Alcohol - 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