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Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/17359

Title: Synthesis and in vitro anticancer screening of some novel 4-[2-amino-3-cyano-4-substituted-5,6,7,8-tetrahydroquinolin-1-(4H)-yl]benzenesulfonamides.
Authors: Mansour S Al-Said
Mostafa M Ghorab
Saleh I Al-Qasoumi
Ebaa M El-Hossary
Eman NoamanEur J Med Chem
Issue Date: 2010
Publisher: PMID
Abstract: It has been reported that aryl/heteroaryl sulfonamide compounds may act as anticancer agents through a variety of mechanisms and the most prominent of these mechanisms is through the inhibition of carbonic anhydrase isozymes. The present work reports the possible utility of 4-(cyclohexenylamino)benzenesulfonamide in the synthesis of some novel 4-(quinolin-1-yl)benzenesulfonamide derivatives 6a-u. The structures of these compounds were confirmed by elemental analyses, IR, (1)H NMR and mass spectral data. All the newly synthesized compounds were evaluated for their in vitro anticancer activity. Some compounds showed interesting in vitro anticancer activities when compared with doxorubicin as a reference drug. In addition, docking of the synthesized compounds into carbonic anhydrase isozyme II (CA II) active site was performed in order to give a suggestion about the proposed mechanism of action. Copyright (c) 2010 Elsevier Masson SAS. All rights reserved. DOI: 10.1016/j.ejmech.2010.03.030
URI: http://hdl.handle.net/123456789/17359
Appears in Collections:College of Pharmacy

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