Structure Information
Structure

Compound Identification

SMILES

C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@@H]3CN[C@@H](C3)C(=O)NCCC3CC[N+](C)(C)CC3)=C(N2C1=O)C([O-])=O

InChIKey

InChIKey=OKSVMQWSVNXWFJ-UUGYHDGCSA-N

Formula

C24H38N4O5S

Mass

494.65

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Lactams

Subclass

Beta lactams

Intermediate Tree Nodes

Carbapenems

Direct Parent

Thienamycins

Alternative Parents

Molecular Framework

Aliphatic heteropolycyclic compounds

Substituents

Thienamycin - Proline or derivatives - Alpha-amino acid amide - Alpha-amino acid or derivatives - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Piperidine - Vinylogous thioester - Tetraalkylammonium salt - Pyrrolidine - Pyrroline - Tertiary carboxylic acid amide - Quaternary ammonium salt - Amino acid or derivatives - Azetidine - Carboxamide group - Carboxylic acid salt - Amino acid - Thioenolether - Secondary carboxylic acid amide - Secondary alcohol - Secondary amine - Sulfenyl compound - Azacycle - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Secondary aliphatic amine - Hydrocarbon derivative - Organonitrogen compound - Organic oxygen compound - Organooxygen compound - Organic nitrogen compound - Carbonyl group - Organosulfur compound - Organic salt - Organic zwitterion - Amine - Alcohol - Organic oxide - Aliphatic heteropolycyclic compound

Description

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.

External Descriptors

Not available

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