Potent and selective neuronal nitric oxide synthase inhibitors with improved cellular permeability

被引:23
|
作者
Xue, Fengtian [1 ,2 ]
Fang, Jianguo [1 ,2 ]
Lewis, William W. [1 ,2 ]
Martasek, Pavel [3 ,4 ,5 ]
Roman, Linda J. [3 ]
Silverman, Richard B. [1 ,2 ]
机构
[1] Northwestern Univ, Chem Life Proc Inst, Dept Chem, Ctr Mol Innovat & Drug Discovery, Evanston, IL 60208 USA
[2] Northwestern Univ, Ctr Mol Innovat & Drug Discovery, Dept Biochem Mol Biol & Cell Biol, Chem Life Proc Inst, Evanston, IL 60208 USA
[3] Univ Texas Hlth Sci Ctr San Antonio, Dept Biochem, San Antonio, TX 78229 USA
[4] Charles Univ Prague, Sch Med 1, Dept Pediat, Prague, Czech Republic
[5] Charles Univ Prague, Sch Med 1, Ctr Appl Genom, Prague, Czech Republic
基金
美国国家卫生研究院;
关键词
Neuronal nitric oxide synthase; Selective inhibitors; Increased membrane permeability; pK(a); MESSENGER-RNA;
D O I
10.1016/j.bmcl.2009.11.086
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Recently, a series of potent and selective neuronal nitric oxide synthase inhibitors containing two basic nitrogen atoms was reported (Ji, H.; Stanton, B. Z.; Igarashi, J.; Li, H.; Martasek, P.; Roman, L. J.; Poulos, T. L.; Silverman, R. B. J. Am. Chem. Soc. 2008, 130, 3900-3914). In an effort to improve their bioavailability, three compounds (2a-c) were designed with electron-withdrawing groups near one of the basic nitrogen atoms to lower its pK(a). Inhibition studies with these compounds showed that two of them not only retained most of the potency and selectivity of the best analogue of the earlier series, but also showed improved membrane permeability based on data from a cell-based assay. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:554 / 557
页数:4
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