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
相关论文
共 50 条
  • [21] The Systemic Administration of Na+/H+ Exchanger-1 Inhibitor Impairs Hippocampal Learning and Memory
    Babur, Ercan
    Canturk, Fatma
    Yaylali, Oguzhan
    Dursun, Nurcan
    Suer, Cem
    JOURNAL OF CLINICAL PRACTICE AND RESEARCH, 2024, 46 (01): : 92 - 97
  • [22] Myocardial Na+/H+ exchanger-1 (NHE1) content is decreased by exercise training
    Bryan J. Feger
    Joseph W. Starnes
    Journal of Physiology and Biochemistry, 2013, 69 : 305 - 312
  • [23] Myocardial Na+/H+ exchanger-1 (NHE1) content is decreased by exercise training
    Feger, Bryan J.
    Starnes, Joseph W.
    JOURNAL OF PHYSIOLOGY AND BIOCHEMISTRY, 2013, 69 (02) : 305 - 312
  • [24] The Na+/H+ exchanger isoform 1
    Fliegel, L
    INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2005, 37 (01): : 33 - 37
  • [25] Design, synthesis and biological evaluation of novel substituted benzoylguanidine derivatives as potent Na+/H+ exchanger inhibitors
    Xu, Wen-Ting
    Jin, Ning
    Xu, Jing
    Xu, Yun-Gen
    Wang, Qiu-Juan
    You, Qi-Dong
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2009, 19 (12) : 3283 - 3287
  • [26] Regulation of myocardial Na+/H+ exchanger activity
    Larry Fliegel
    Basic Research in Cardiology, 2001, 96 : 301 - 305
  • [27] Regulation of myocardial Na+/H+ exchanger activity
    Fliegel, L
    BASIC RESEARCH IN CARDIOLOGY, 2001, 96 (04) : 301 - 305
  • [28] Synthesis and biological activity of N-(aminoiminomethyl)-1H-indole carboxamide derivatives as Na+/H+ exchanger inhibitors
    Kitano, M
    Kojima, A
    Nakano, K
    Miyagishi, A
    Noguchi, T
    Ohashi, N
    CHEMICAL & PHARMACEUTICAL BULLETIN, 1999, 47 (11) : 1538 - 1548
  • [29] The Na+/H+ exchanger in metastasis
    Amith, Schammim Ray
    Fliegel, Larry
    AGING-US, 2016, 8 (07): : 1291 - 1291
  • [30] Na+/H+ exchanger-1 inhibitors decrease myocardial superoxide production via direct mitochondrial action
    Garciarena, Carolina D.
    Caldiz, Claudia I.
    Correa, Maria V.
    Schinella, Guillermo R.
    Mosca, Susana M.
    de Cingolani, Gladys E. Chiappe
    Cingolani, Horacio E.
    Ennis, Irene L.
    JOURNAL OF APPLIED PHYSIOLOGY, 2008, 105 (06) : 1706 - 1713