C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@@H]3CN[C@@H](C3)C3CNCC(=O)N3)=C(N2C1=O)C(O)=O

InChIKey=RZXLDPMXPMUMLL-DXWFBNGCSA-N

C18H26N4O5S

410.49

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

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

Aliphatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid amide - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - 1,4-diazinane - Piperazine - Vinylogous thioester - Pyrrolidine - Tertiary carboxylic acid amide - Pyrroline - Amino acid or derivatives - Azetidine - Carboxamide group - Amino acid - Thioenolether - Secondary carboxylic acid amide - Secondary alcohol - Secondary amine - Sulfenyl compound - Azacycle - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Secondary aliphatic amine - Carboxylic acid - Organosulfur compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Amine - Alcohol - 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