Salicylaldoxime derivatives as new leads for the development of carbonic anhydrase inhibitors

被引：12
|
作者：
Tuccinardi, Tiziano [1 ]
Bertini, Simone [1 ]
Granchi, Carlotta [1 ]
Ortore, Gabriella [1 ]
Macchia, Marco [1 ]
Minutolo, Filippo [1 ]
Martinelli, Adriano [1 ]
Supuran, Claudiu T. [2 ]
机构：
[1] Univ Pisa, Dipartimento Sci Farmaceut, I-56126 Pisa, Italy
[2] Univ Florence, Lab Chim Bioinorgan, I-50019 Florence, Italy
来源：
BIOORGANIC & MEDICINAL CHEMISTRY | 2013年 / 21卷 / 06期
关键词：
Carbonic anhydrase; Salicylaldoxime; Docking; QM/MM calculation; Zinc binding group; ACTIVATORS; LIGANDS; DESIGN; QM/MM;
D O I：
10.1016/j.bmc.2012.08.057
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
New compounds containing a novel zinc binding group (salicylaldoxime system) were identified as effective inhibitors of carbonic anhydrases (CAs). This structural motif seems to bind the catalytic zinc ion of CAs, revealing itself as a new valid alternative to the sulfonamide group. Computational procedures were used to investigate the binding mode of this class of compounds, within the active site of CAII. This study suggests that the salicylaldoxime moiety binds the zinc ion through the oxime oxygen atom that also forms an H-bond with T199. The results herein obtained will allow the development of new CA-inhibitors bearing the salicylaldoxime moiety. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码：1511 / 1515
页数：5
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