Design, synthesis and molecular docking of novel N,N-dimethylbenzenesulfonamide derivatives as potential antiproliferative agents-Reference-Cited by-同舟云学术

Design, synthesis and molecular docking of novel N,N-dimethylbenzenesulfonamide derivatives as potential antiproliferative agents

Published:2013-10-03 Issue:5 Volume:29 Page:619-627
ISSN:1475-6366
Container-title:Journal of Enzyme Inhibition and Medicinal Chemistry
language:en
Short-container-title:Journal of Enzyme Inhibition and Medicinal Chemistry

Author:

Bashandy Mahmoud S.¹,Alsaid Mansour S.²,Arafa Reem K.³,Ghorab Mostafa M.²⁴

Affiliation:

1. Department of Chemistry, Faculty of Science, Al-Azhar University Nasr City, CairoEgypt

2. Department of Pharmacognosy, College of Pharmacy, King Saud University RiyadhKingdom of Saudi Arabia

3. Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Cairo University CairoEgypt

4. Deprtment of Drug Radiation Research, National Center for Radiation Research and Technology, Atomic Energy CairoEgypt

Publisher

Informa UK Limited

Subject

Drug Discovery,Pharmacology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.3109/14756366.2013.833197

Reference30 articles.

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4. 20:388-400. (c) Ghorab MM, Ragab FA, Heiba HI, et al. In vitro anticancer screening and radiosensitizing evaluation of some new quinolines and pyrimido[4,5-b]quinolines bearing a sulfonamide moiety. Eur J Med Chem 2010;45:3677-84. (d) Abbate F, Casini A, Owa T, et al. Carbonic anhydrase inhibitors: E7070, a sulfonamide anticancer agent, potently inhibits cytosolic isozymes I and II, and transmembrane, tumor-associated isozyme IX. Bioorg Med Chem Lett 2004;14:217-23. (e) Stephens CE, Felder TM, Sowell JW, et al. Synthesis and antiviral/antitumor evaluation of 2-amino- and 2-carboxamido-3-arylsulfonylthiophenes and related compounds as a new class of diarylsulfones. Bioorg Med Chem 2001;9:1123-32

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