CNCC1=CC=C(C=C1)[C@@H]1C[C@@H](CN1)SC1=C(N2[C@@H]([C@@H]([C@@H](C)O)C2=O)[C@H]1C)C(O)=O

InChIKey=ZYCHALGBMHRNST-QKZKPRJSSA-N

C22H29N3O4S

431.55

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Carbapenems

Thienamycins

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

Aromatic heteropolycyclic compounds

Thienamycin - 2-phenylpyrrolidine - Alpha-amino acid or derivatives - Benzylamine - Phenylmethylamine - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Aralkylamine - Monocyclic benzene moiety - Vinylogous thioester - Benzenoid - Pyrrole - Pyrrolidine - Tertiary carboxylic acid amide - Pyrroline - Amino acid or derivatives - Azetidine - Amino acid - Carboxamide group - Thioenolether - Secondary alcohol - Secondary amine - Sulfenyl compound - Azacycle - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Monocarboxylic acid or derivatives - Alcohol - Carbonyl group - Amine - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Aromatic 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