Design, synthesis, cytotoxic evaluation and molecular docking of novel 1, 3, 4-thiadiazole sulfonamides with azene and coumarin moieties as carbonic anhydrase inhibitors-Reference-Cited by-同舟云学术

Design, synthesis, cytotoxic evaluation and molecular docking of novel 1, 3, 4-thiadiazole sulfonamides with azene and coumarin moieties as carbonic anhydrase inhibitors

Published:2023-08 Issue:8 Volume:16 Page:104956
ISSN:1878-5352
Container-title:Arabian Journal of Chemistry
language:en
Short-container-title:Arabian Journal of Chemistry

Author:

Bondock Samir,Albarqi Tallah,Nasr Tamer,Mohamed Nada M.,Abdou Moaz M.

Funder

Deanship of Scientific Research, King Khalid University

Publisher

Elsevier BV

Subject

General Chemical Engineering,General Chemistry

Reference49 articles.

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3. S. Bilginer, H. I. G., B. Anil, 2020. Synthesis and in silico studies of triazene-substituted sulfamerazine derivatives as acetylcholinesterase and carbonic anhydrases inhibitors. Archiv der Pharmazie. 354

4. Bioinformatics, S. I. o., 2017. SwissADME: a free web tool to evaluate pharmacokinetics, drug-likeness and medicinal chemistry friendliness of small molecules. Sci. Rep. . 7, 42717

5. J. Boix, N. L., V.Yuste, 1997. Characterization of the cell death process induced by staurosporine in human neuroblastoma cell lines. Neuropharmacology. 36, 811-821

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