兰尼定受体
基因亚型
化学
亲缘关系
合理设计
功能(生物学)
生物
计算生物学
生物化学
细胞生物学
受体
基因
遗传学
作者
John L. Sutko,Judith A. Airey,William R. Welch,Luc Ruest
出处
期刊:PubMed
日期:1997-03-01
卷期号:49 (1): 53-98
被引量:96
摘要
The goal of this review has been to describe the current state of the pharmacology of ryanodine and related compounds relative to the vertebrate RyRs. Resolution of questions concerning the molecular properties of RyR channel function and the contributions made by the RyR isoforms to cellular signaling in a variety of tissues will require the production of new pharmacological agents directed against these proteins. Novel naturally occurring ryanodine congeners have been identified, and significant advances have been made in developing chemical approaches that permit the structure of ryanodine to be derivatized in selective ways. Moreover, several of these changes have yielded compounds that differ in their binding affinities and in their abilities to modify the properties of the RyR channels. These advances give substance to the possibility of designing the required pharmacological agents based on rational design changes of the structure ryanodine.
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