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首页> 外文期刊>Japanese Journal of Pharmacology >Molecular Pharmacology of T-type Ca2+ Channels
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Molecular Pharmacology of T-type Ca2+ Channels

机译:T型Ca2 +通道的分子药理作用

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References(100) Cited-By(45) Over the past few years increasing attention has been focused on T-type calcium channels and their possible physiological and pathophysiological roles. Efforts toward elucidating the exact role(s) of these calcium channels have been hampered by the lack of T-type specific antagonists, resulting in the subsequent use of less selective calcium channel antagonists. In addition, the activity of these blockers often varies with cell or tissue type, as well as recording conditions. This review summarizes a variety of compounds that exhibit varying degrees of blocking activity towards T-type Ca2+ channels. It is designed as an aid for researchers in need of antagonists to study the biophysical and pathological nature of T-type channels, as well as a starting point for those attempting to develop potent and selective antagonists of the channel.
机译:参考文献(100)被引用(45)在过去的几年中,人们越来越关注T型钙通道及其可能的生理和病理生理作用。缺乏T型特异性拮抗剂阻碍了阐明这些钙通道确切作用的努力,导致随后使用选择性较低的钙通道拮抗剂。另外,这些阻滞剂的活性通常随细胞或组织类型以及记录条件而变化。这篇综述总结了对T型Ca2 +通道表现出不同程度的阻断活性的各种化合物。它旨在帮助需要拮抗剂的研究人员研究T型通道的生物物理和病理学性质,以及为那些试图开发有效和选择性通道拮抗剂的人们提供一个起点。

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