Benzamide derivatives as blockers of Kv1.3 ion channel

Bioorg Med Chem Lett. 2003 Mar 24;13(6):1161-4. doi: 10.1016/s0960-894x(03)00014-3.

Abstract

The voltage-gated potassium channel, Kv1.3, is present in human T-lymphocytes. Blockade of Kv1.3 results in T-cell depolarization, inhibition of T-cell activation, and attenuation of immune responses in vivo. A class of benzamide Kv1.3 channel inhibitors has been identified. The structure-activity relationship within this class of compounds in two functional assays, Rb_Kv and T-cell proliferation, is presented. In in vitro assays, trans isomers display moderate selectivity for binding to Kv1.3 over other Kv1.x channels present in human brain.

MeSH terms

  • Benzamides / chemical synthesis*
  • Benzamides / pharmacology*
  • Brain Chemistry / drug effects
  • Cell Division / drug effects
  • Humans
  • In Vitro Techniques
  • Kv1.3 Potassium Channel
  • Potassium Channel Blockers / chemical synthesis*
  • Potassium Channel Blockers / pharmacology*
  • Potassium Channels / drug effects*
  • Potassium Channels, Voltage-Gated*
  • Rubidium Radioisotopes
  • Stereoisomerism
  • Structure-Activity Relationship
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / metabolism

Substances

  • Benzamides
  • KCNA3 protein, human
  • Kv1.3 Potassium Channel
  • Potassium Channel Blockers
  • Potassium Channels
  • Potassium Channels, Voltage-Gated
  • Rubidium Radioisotopes