Structure Information
Structure

Compound Identification

SMILES

CC(O)C1C2C(C)C(SC3CC(N(C3)C(O)=O)C(=O)NC3=CC=CC(=C3)C(O)=O)=C(N2C1=O)C(O)=O

InChIKey

InChIKey=QGOHILCWOMQGLM-UHFFFAOYSA-N

Formula

C23H25N3O9S

Mass

519.53

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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

Aromatic heteropolycyclic compounds

Substituents

Thienamycin - Acylaminobenzoic acid or derivatives - Proline or derivatives - Alpha-amino acid amide - Alpha-amino acid or derivatives - Benzoic acid or derivatives - Benzoic acid - Anilide - Benzoyl - Pyrrolidine carboxylic acid - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - N-arylamide - Azepine - Vinylogous thioester - Benzenoid - Monocyclic benzene moiety - Pyrroline - Pyrrolidine - Tertiary carboxylic acid amide - Secondary carboxylic acid amide - Secondary alcohol - Azetidine - Carbamic acid - Carbamic acid derivative - Thioenolether - Carboxamide group - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Azacycle - Sulfenyl compound - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic nitrogen compound - Aromatic 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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