Synthesis and carbonic anhydrase inhibitory properties of novel cyclohexanonyl bromophenol derivatives.
Halis T Balaydın, Murat Sentürk, Abdullah Menzek
Index: Bioorg. Med. Chem. Lett. 22 , 1352-7, (2012)
Full Text: HTML
Abstract
The Naturally occurring novel cyclohexanonyl bromophenol 2(R)-2-(2,3,6-tribromo-4,5-dihydroxybenzyl)cyclohexanone (4) was synthesized as a racemic compound. Cyclohexylphenyl methane derivatives (10-17) with Br, OMe, CO, and OH were also obtained. Inhibition of four human carbonic anhydrase (hCA, EC 4.2.1.1) isozymes I, II, IV, and VI, with compounds 2-4, 8, and 10-26 was investigated. These compounds were found to be promising carbonic anhydrase inhibitors and some of them showed interesting inhibitory activity. Some of the compounds investigated here showed effective hCA inhibitory activity, and might be used as leads for generating novel carbonic anhydrase inhibitors which are valuable drug candidates for the treatment of glaucoma, epilepsy, gastric and duodenal ulcers, neurological disorders, and osteoporosis.Copyright © 2011 Elsevier Ltd. All rights reserved.
Related Compounds
Related Articles:
2015-07-01
[J. Food Sci. 80 , C1476-89, (2015)]
2011-02-15
[Bioorg. Med. Chem. 19 , 1381-9, (2011)]
2005-10-27
[J. Phys. Chem. A 109(42) , 9456-64, (2005)]
2009-06-04
[Org. Lett. 11(11) , 2253-6, (2009)]
2010-10-28
[J. Phys. Chem. A 114(42) , 11144-52, (2010)]