C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@H]3C[C@H](N(C3)C(=O)OCC=C)C(=O)N3CCC(CC3)=NO)=C(N2C1=O)C(=O)OCC=C

InChIKey=ZYUSFBWJUVANJW-ISHYOLQKSA-N

C27H36N4O8S

576.67

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

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

Aliphatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid amide - Alpha-amino acid or derivatives - N-acyl-piperidine - Pyrrolidine carboxylic acid - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Piperidine - Vinylogous thioester - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Pyrrolidine - Carbamic acid ester - Pyrroline - Tertiary carboxylic acid amide - Carboxylic acid ester - Carboxamide group - Thioenolether - Azetidine - Secondary alcohol - Monocarboxylic acid or derivatives - Sulfenyl compound - Azacycle - Carboxylic acid derivative - Oxime - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organosulfur compound - Alcohol - Organic nitrogen compound - Organic oxygen 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