C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(SC3CN(C3)C3=NCCS3)=C(N2C1=O)C(=O)OCOC(=O)C(C)(C)C

InChIKey=SNUDIPVBUUXCDG-QHSBEEBCSA-N

C22H31N3O6S2

497.63

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

Alpha amino acids and derivatives Pyrroline carboxylic acids Acylals Azepines Vinylogous thioesters Dicarboxylic acids and derivatives Thiazolines Tertiary carboxylic acid amides Enoate esters Thioenol ethers Secondary alcohols Azetidines Isothioureas Propargyl-type 1,3-dipolar organic compounds Carboximidamides Sulfenyl compounds Acetals Azacyclic compounds Carbonyl compounds Organopnictogen compounds Hydrocarbon derivatives Organic oxides

Aliphatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Acylal - Dicarboxylic acid or derivatives - Vinylogous thioester - Pyrroline - Tertiary carboxylic acid amide - Meta-thiazoline - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Azetidine - Carboxamide group - Carboxylic acid ester - Isothiourea - Secondary alcohol - Thioenolether - Azacycle - Carboximidamide - Sulfenyl compound - Acetal - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carboxylic acid derivative - Hydrocarbon derivative - Organopnictogen compound - Organic nitrogen compound - Alcohol - Carbonyl group - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organosulfur 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