C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(SC3CNC(=O)C3)=C(N2C1=O)C(=O)OC(C)OC(=O)OC1CCCC1

InChIKey=DDPMHAJFCXQVBX-GSIXIDEFSA-N

C22H30N2O8S

482.55

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Azepines Vinylogous thioesters Carbonic acid diesters Pyrrolidine-2-ones Tertiary carboxylic acid amides Enoate esters Thioenol ethers Azetidines Secondary carboxylic acid amides Secondary alcohols Sulfenyl compounds Azacyclic compounds Acetals Monocarboxylic acids and derivatives Hydrocarbon derivatives Carbonyl compounds Organic oxides Organonitrogen compounds Organopnictogen compounds

Aliphatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Pyrrolidone - Carbonic acid diester - 2-pyrrolidone - Vinylogous thioester - Pyrrolidine - Alpha,beta-unsaturated carboxylic ester - Pyrroline - Tertiary carboxylic acid amide - Enoate ester - Secondary alcohol - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid ester - Thioenolether - Azetidine - Carbonic acid derivative - Acetal - Carboxylic acid derivative - Azacycle - Monocarboxylic acid or derivatives - Sulfenyl compound - Alcohol - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organosulfur 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