Synthesis and Na+/H+ Exchanger-1 Inhibitory Activity of Substituted (Quinolinecarbonyl)guanidine Derivatives

被引:10
|
作者
Mao, Dan [1 ]
Xu, Yungen [1 ]
Hu, Xiaoping [1 ]
Zhang, Guomin [2 ]
Dong, Jin [1 ]
Gong, Guoqing [2 ]
机构
[1] China Pharmaceut Univ, Dept Med Chem, Nanjing 210009, Peoples R China
[2] China Pharmaceut Univ, Dept Pharmacol, Nanjing 210009, Peoples R China
关键词
REPERFUSION; ISCHEMIA;
D O I
10.1002/cbdv.200800268
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
The Na+/H+ exchanger (NHE) is a protein expressed in many mammalian cell types. It is involved in intracellular pH (pH(i)) homeostasis by exchanging extracellular Na+ for intracellular H+. To date, nine NHE isoforms (NHE1-NHE9) have been identified. NHE1 is the most predominant isoform expressed in mammalian cardiac muscle. A novel series of substituted (quinolinecarbonyl)guanidine derivatives were designed and synthesized as NHE inhibitors. Most compounds can inhibit NHE1-mediated platelet swelling in a concentration-dependent manner, among which compound 7f was the most active and more potent than cariporide. Furthermore, compound 7f has also been demonstrated to exhibit the in vivo cardioprotective effects against SD rat myocardial ischemic-reperfusion injury superior to those of cariporide.
引用
收藏
页码:1727 / 1736
页数:10
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