T-type calcium channels inhibitors: a patent review

被引:37
|
作者
Giordanetto, Fabrizio [1 ]
Knerr, Laurent [1 ]
Wallberg, Andreas [1 ]
机构
[1] AstraZeneca R&D, Lead Generat, SE-43183 Molndal, Sweden
关键词
calcium channel inhibition; Ca(v)3; mibefradil; T-type calcium channels; VOLTAGE-GATED CALCIUM; CA2+ CHANNEL; BIOLOGICAL EVALUATION; MIBEFRADIL; BLOCKERS; DERIVATIVES; DESIGN; DISCOVERY; NEURONS; CELLS;
D O I
10.1517/13543776.2011.536532
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Importance of the field: T-type calcium channels are transmembrane proteins that regulate calcium entry in the cell in a voltage-dependent manner. Intracellular calcium levels are the key to many physiological processes, ranging from neuron firing to cardiac pacemaking. Inhibition of T-type calcium channels is heralded as a potential treatment to peripheral and CNS disorders, including hypertension, heart failure, sleep, epilepsy, drug addiction and neuropathic pain. Areas covered in this review: A comprehensive summary of patent literature disclosing T-type calcium channels inhibitors is provided. What the reader will gain: In all, 46 patent applications including 15 chemical structure classes are reviewed. Available in vitro, in vivo and clinical results are also discussed. Take home message: Several selective T-type calcium channels inhibitors with demonstrated in vitro and in vivo effects, including one Phase I clinical candidate, are now available. While future clinical results will be paramount to assess target validity in patients, these novel inhibitors represent excellent tools to further investigate the role of T-type channels in pathophysiological conditions.
引用
收藏
页码:85 / 101
页数:17
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