C[C@@H](O)[C@@H]1[C@H]2CC(S[C@H]3CC[N+](C3)=C(C)N)=C(N2C1=O)C(O)=O

InChIKey=TYMABNNERDVXID-DLYFRVTGSA-O

C15H22N3O4S

340.42

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

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

Aliphatic heteropolycyclic compounds

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Vinylogous thioester - Pyrrolidine - Tertiary carboxylic acid amide - Pyrroline - Amino acid or derivatives - Amino acid - Azetidine - Carboxamide group - Thioenolether - Tertiary amine - Secondary alcohol - Amidine - Carboxylic acid amidine - Azacycle - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Sulfenyl compound - Carboximidamide - Alcohol - Organic nitrogen compound - Carbonyl group - Amine - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxide - Hydrocarbon derivative - Organic cation - 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