Structure Information
Structure

Compound Identification

SMILES

[Na+].C[C@@H](O)C1C2[C@@H](C)C(SC3CN(C3)C3=NC(=CS3)C(=O)NC3CC3)=C(N2C1=O)C([O-])=O

InChIKey

InChIKey=XJNVSYCNKOIRKF-LTXDTYCBSA-M

Formula

C20H23N4NaO5S2

Mass

486.54

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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 - Alpha-amino acid or derivatives - 2-heteroaryl carboxamide - Thiazolecarboxylic acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Thiazolecarboxamide - Dialkylarylamine - 2,4-disubstituted 1,3-thiazole - Azepine - 1,3-thiazol-2-amine - Vinylogous thioester - Tertiary carboxylic acid amide - Pyrroline - Heteroaromatic compound - Azole - Thiazole - Azetidine - Carboxamide group - Carboxylic acid salt - Secondary alcohol - Secondary carboxylic acid amide - Thioenolether - Sulfenyl compound - Organic alkali metal salt - Azacycle - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxide - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organosulfur compound - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - Amine - Organic salt - Organic zwitterion - Organic sodium salt - 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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