Coumarins and other fused bicyclic heterocycles with selective tumor-associated carbonic anhydrase isoforms inhibitory activity

Herein we report for the first time a series of 2-benzamido-N-(2-oxo-4-(methyl/trifluoromethyl)-2H-chromen-7-yl) benzamide 3a–f and substituted quinazolin-4(3H)-ones and 2H-benzo[e][1,2,4]thiadiazin-3(4H)-one 1,1-dioxides (5, 6, 8 and 10a–c) as selective inhibitors of the tumor associated hCA IX and...

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Main Authors: Bozdag, Murat, Alafeefy, Ahmed Mahmoud, Altamimi, Abdul Malik, Vullo, Daniela, Carta, Fabrizio, Supuran,, Claudiu T.
Format: Article
Language:en
en
en
Published: Elsevier Ltd 2017
Subjects:
Online Access:http://irep.iium.edu.my/56574/1/56574_Coumarins%20and%20other%20fused%20bicyclic_text.pdf
http://irep.iium.edu.my/56574/2/56574_Coumarins%20and%20other%20fused%20bicyclic_SCOPUS.pdf
http://irep.iium.edu.my/56574/13/56574_Coumarins%20and%20other%20fused%20bicyclic%20heterocycles_WOS.pdf
http://irep.iium.edu.my/56574/
http://www.sciencedirect.com/science/article/pii/S0968089616311051
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Summary:Herein we report for the first time a series of 2-benzamido-N-(2-oxo-4-(methyl/trifluoromethyl)-2H-chromen-7-yl) benzamide 3a–f and substituted quinazolin-4(3H)-ones and 2H-benzo[e][1,2,4]thiadiazin-3(4H)-one 1,1-dioxides (5, 6, 8 and 10a–c) as selective inhibitors of the tumor associated hCA IX and XII isoforms. Among the compounds reported the trifluoromethyl derivative 3d resulted the most potent against these CA isoforms with KIs of 10.9 and 6.7 nM