神经科学
同色
烟碱激动剂
烟碱乙酰胆碱受体
乙酰胆碱受体
精神分裂症(面向对象编程)
中枢神经系统
药理学
医学
生物
受体
生物化学
精神科
内科学
蛋白质亚单位
基因
作者
Corinne Beinat,Samuel D. Banister,Marco Herrera-Barrera,Michael Kassiou
标识
DOI:10.2174/1381612822666160127114125
摘要
Homomeric α7 nicotinic acetylcholine receptors (nAChRs) are implicated in the regulation of cognitive processes such as memory and attention and have potential as therapeutic targets for the treatment of the cognitive deficits associated with schizophrenia. Though numerous α7 nAChR agonists have been developed, and several have progressed to clinical trials, these are derived from few common chemotypes. Consequently, many of these α7 nAChR clinical candidates share unfavorable side-effect profile. SEN12333 represents a novel chemotype for the development of α7 nAChR agonists, and exploration of this scaffold has produced structurally diverse ligands with promising pharmacological properties. This review will summarize structure-affinity and -activity relationships surrounding analogs of SEN12333.
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