Current Strategies for the Discovery of K+ Channel Modulators

被引:7
|
作者
Ye, Deju [1 ]
Wang, Jiang [1 ]
Yu, Kunqian [1 ]
Zhou, Yu [1 ]
Jiang, Hualiang [1 ,2 ]
Chen, Kaixian [1 ]
Liu, Hong [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Shanghai Inst Mat Med, State Key Lab Drug Res,Ctr Drug Discovery & Desig, Shanghai 201203, Peoples R China
[2] E China Univ Sci & Technol, Sch Pharm, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
Potassium channels; modulator; blocker; opener; virtual screening; chemistry strategy; MAOS; KV1.5 POTASSIUM CHANNEL; 1,4-BENZOXAZINE DERIVATIVES; DYNAMICS SIMULATIONS; CRYSTAL-STRUCTURE; DRUG DISCOVERY; ION CHANNELS; IN-VIVO; BLOCKERS; CHEMISTRY; SHAKER;
D O I
10.2174/156802609788317865
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Potassium ion (K+) channels consist of a ubiquitous family of membrane proteins that play critical roles in a wide variety of physiological processes, such as the regulation of neuronal excitability, muscle contraction, cell proliferation, and insulin secretion. Due to their pivotal functions in biological systems, K+ channels have long been attractive targets for the rational drug design on the basis of their structures and interaction mechanisms. Various small-molecular compounds and toxins have been discovered to act as K+ channel modulators. In the present review, we will first briefly discuss current knowledge of the structures and functions of K+ channels, and then review the recent strategies for the discovery of K+ channel modulators, focusing especially on the virtual screening approaches and chemical synthesis technologies.
引用
收藏
页码:348 / 361
页数:14
相关论文
共 50 条
  • [11] Strategies To Reduce hERG K+ Channel Blockade. Exploring Heteroaromaticity and Rigidity in Novel Pyridine Analogues of Dofetilide
    Carvalho, Joao F. S.
    Louvel, Julien
    Doornbos, Maarten L. J.
    Klaasse, Elisabeth
    Yu, Zhiyi
    Brussee, Johannes
    IJzerman, Adriaan P.
    JOURNAL OF MEDICINAL CHEMISTRY, 2013, 56 (07) : 2828 - 2840
  • [12] K+ channel alterations in the progression of experimental autoimmune encephalomyelitis
    Jukkola, Peter I.
    Lovett-Racke, Amy E.
    Zamvil, Scott S.
    Gu, Chen
    NEUROBIOLOGY OF DISEASE, 2012, 47 (02) : 280 - 293
  • [13] Lipid Bilayer Modules as Determinants of K+ Channel Gating
    Syeda, Ruhma
    Santos, Jose S.
    Montal, Mauricio
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2014, 289 (07) : 4233 - 4243
  • [14] Comparative effects of sophocarpine and sophoridine on hERG K+ channel
    Zhao, Xue Ling
    Gu, Dong Fang
    Qi, Zhi Ping
    Chen, Ming Hong
    Wei, Ting
    Li, Bao Xin
    Yang, Bao Feng
    EUROPEAN JOURNAL OF PHARMACOLOGY, 2009, 607 (1-3) : 15 - 22
  • [15] Ether-a-go-go K+ channels: effective modulators of neuronal excitability
    Bauer, Christiane K.
    Schwarz, Juergen R.
    JOURNAL OF PHYSIOLOGY-LONDON, 2018, 596 (05): : 769 - 783
  • [16] A computational design approach for virtual screening of peptide interactions across K+ channel families
    Doupnik, Craig A.
    Parra, Katherine C.
    Guida, Wayne C.
    COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL, 2015, 13 : 85 - 94
  • [17] Conorfamide-Sr3, a structurally novel specific inhibitor of the Shaker K+ channel
    Campos-Lira, Elba
    Carrillo, Elisa
    Aguilar, Manuel B.
    Gajewiak, Joanna
    Gomez-Lagunas, Froylan
    Lopez-Vera, Estuardo
    TOXICON, 2017, 138 : 53 - 58
  • [18] A channel profile report of the unusual K+ channel KtrB
    Mikusevic, Vedrana
    Schrecker, Marina
    Kolesova, Natalie
    Patino-Ruiz, Miyer
    Fendler, Klaus
    Haenelt, Inga
    JOURNAL OF GENERAL PHYSIOLOGY, 2019, 151 (12) : 1357 - 1368
  • [19] Clustering of the K+ channel GORK of Arabidopsis parallels its gating by extracellular K+
    Eisenach, Cornelia
    Papanatsiou, Maria
    Hillert, Ellin-Kristina
    Blatt, Michael R.
    PLANT JOURNAL, 2014, 78 (02) : 203 - 214
  • [20] Microglial K+ Channel Expression in Young Adult and Aged Mice
    Schilling, Tom
    Eder, Claudia
    GLIA, 2015, 63 (04) : 664 - 672