Discovery and functional characterization of N-(thiazol-2-yl)-benzamide analogs as the first class of selective antagonists of the Zinc-Activated Channel (ZAC)
Author:
Funder
National Institute of Mental Health
National Institute of Neurological Disorders and Stroke
Danish Council for Independent Research
Publisher
Elsevier BV
Subject
Pharmacology,Biochemistry
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Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Evolutionary conservation of Zinc-Activated Channel (ZAC) functionality in mammals: a range of mammalian ZACs assemble into cell surface-expressed functional receptors;Frontiers in Molecular Biosciences;2023-09-04
2. Probing the molecular basis for signal transduction through the Zinc-Activated Channel (ZAC);Biochemical Pharmacology;2021-11
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