Synthesis, anticancer, antimicrobial, anti-tuberculosis and molecular docking of heterocyclic N-ethyl-N-methylbenzenesulfonamide derivatives-Reference-Cited by-同舟云学术

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Synthesis, anticancer, antimicrobial, anti-tuberculosis and molecular docking of heterocyclic N-ethyl-N-methylbenzenesulfonamide derivatives

Published:2020-03 Issue: Volume:1203 Page:127423
ISSN:0022-2860
Container-title:Journal of Molecular Structure
language:en
Short-container-title:Journal of Molecular Structure

Author:

Debbabi Khaled F.,Al-Harbi Sami A.,Al-Saidi Hamed M.,Aljuhani Enas H.,Felaly Rasha N.,Abd El-Gilil Shimaa M.,Bashandy Mahmoud S.,Jannet Hichem ben

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference50 articles.

1. Molecular strategies for overcoming antibiotic resistance in bacteria;Tan;Mol. Med. Today,2000

2. Sulfonamides incorporating heteropolycyclic scaffolds show potent inhibitory action against carbonic anhydrase isoforms I, II, IX and XII;Barresi;Bioorg. Med. Chem.,2016

3. Syntheses, spectroscopic investigation and electronic properties of two sulfonamide derivatives: a combined experimental and quantum chemical approach;Mahmood;J. Mol. Struct.,2016

4. Development of certain new 2-substituted-quinazolin-4-yl-aminobenzenesulfonamide as potential antitumor agents;Alafeefy;Eur. J. Med. Chem.,2016

5. Designing of novel carbonic anhydrase inhibitors and activators;Supuran;Curr. Med. Chem. Cardiovasc. Hematol. Agents,2004

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