Channelpedia

PubMed 15357987


Referenced in Channelpedia wiki pages of: none

Automatically associated channels: KCNQ2 , Kv7.2



Title: Synthesis and KCNQ2 opener activity of N-(1-benzo[1,3]dioxol-5-yl-ethyl, N-[1-(2,3-dihydro-benzofuran-5-yl)-ethyl, and N-[1-(2,3-dihydro-1H-indol-5-yl)-ethyl acrylamides.

Authors: Yong-Jin Wu, Li-Qiang Sun, Huan He, Jie Chen, John E Starrett, Pierre Dextraze, Jean-Paul Daris, Christopher G Boissard, Rick L Pieschl, Valentin K Gribkoff, Joanne Natale, Ronald J Knox, David G Harden, Mark W Thompson, William Fitzpatrick, David Weaver, Dedong Wu, Qi Gao, Steven I Dworetzky

Journal, date & volume: Bioorg. Med. Chem. Lett., 2004 Sep 6 , 14, 4533-7

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/15357987


Abstract
Bioisosteric replacement studies led to the identification of N-(1-benzo[1,3]dioxol-5-yl-ethyl)-3-(2-chloro-phenyl)-acrylamide ((S)-3) as a highly potent KCNQ2 opener, and 3-(2,6-difluoro-phenyl)-N-[1-(2,3-dihydro-benzofuran-5-yl)-ethyl]-acrylamide ((S)-4), and N-[1-(2,3-dihydro-1H-indol-5-yl)-ethyl]-3-(2-fluoro-phenyl)-acrylamide ((S)-5) as highly efficacious KCNQ2 openers. In contrast, their respective R enantiomers showed significantly less or no appreciable KCNQ2 opener activity even at the highest concentration tested (10 microM). Because of its high potency and moderate efficacy as well as its convenient synthesis, (+/-)-3 was selected as a reference compound for analyzing efficacies of KCNQ openers in electrophysiology studies. Compounds (S)-4 and (S)-5 demonstrated significant activity in reducing neuronal hyperexcitability in rat hippocampal slices. The synthesis and the KCNQ2 opener activity of these acrylamides are described.