CHARACTERIZING THE ROLE OF T352 IN THE INHIBITION OF THE LARGE CONDUCTANCE Ca-ACTIVATED K (BK) CHANNELS BY 1-[1-HEXYL-6-(METHYLOXY)- 1H-INDAZOL-3-YL]-2-METHYL-1-PROPANONE (HMIMP)

Abstract

1 CHARACTERIZING THE ROLE OF T352 IN THE INHIBITION OF THE LARGE CONDUCTANCE Ca-ACTIVATED K (BK) CHANNELS BY 1-[1-HEXYL-6-(METHYLOXY)1H-INDAZOL-3-YL]-2-METHYL-1-PROPANONE (HMIMP) Earl Gordon, Simon F. Semus, Irina M. Lozinskaya, Zuojun Lin, and Xiaoping Xu From Metabolic Pathways Center of Excellence in Drug Discovery (E.G., I.M.L., Z.L., X.X.) and Department of Computational and Structural Chemistry (S.F.S.), GlaxoSmithKline Pharmaceuticals, King of Prussia, PA 19406 JPET Fast Forward. Published on April 29, 2010 as DOI:10.1124/jpet.110.166017

Cite this paper

@inproceedings{JPET2010CHARACTERIZINGTR, title={CHARACTERIZING THE ROLE OF T352 IN THE INHIBITION OF THE LARGE CONDUCTANCE Ca-ACTIVATED K (BK) CHANNELS BY 1-[1-HEXYL-6-(METHYLOXY)- 1H-INDAZOL-3-YL]-2-METHYL-1-PROPANONE (HMIMP)}, author={JPET and Earl Gordon and Simon F. Semus and Irina M. Lozinskaya and Zuojun Lin and Xiaoping Xu}, year={2010} }