Title : Molecular pharmacology of human Cav3.2 T-type Ca2+ channels: block by antihypertensives, antiarrhythmics, and their analogs.

Pub. Date : 2009 Feb

PMID : 18974361






1 Functional Relationships(s)
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1 The goal of this study was to identify compounds that block the Ca(v)3.2 T-type channel with high affinity, focusing on two classes of compounds: phenylalkylamines (e.g., mibefradil) and dihydropyridines (e.g., efonidipine). Mibefradil immunoglobulin lambda variable 7-43 Homo sapiens