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Small molecule antagonists of the vanilloid receptor 1 (TRPV1, also known as VR1) are disclosed. Ureas such as 5 (SB-452533) were used to explore the structure activity relationship with several potent analogues identified. Pharmacological studies using electrophysiological and FLIPR Ca(2+) based assays showed compound 5 was an antagonist versus capsaicin, noxious heat and acid mediated activation of TRPV1. Study of a quaternary salt of 5 supports a mode of action in which compounds from this series cause inhibition via an extracellularly accessible binding site on the TRPV1 receptor.

Original publication

DOI

10.1016/j.bmcl.2004.05.028

Type

Journal article

Journal

Bioorg Med Chem Lett

Publication Date

16/07/2004

Volume

14

Pages

3631 - 3634

Keywords

Aminobiphenyl Compounds, Animals, Binding Sites, Calcium, Capsaicin, Cell Line, Electrophysiology, Fluorescence, Hot Temperature, Humans, Hydrogen-Ion Concentration, Image Enhancement, Patch-Clamp Techniques, Rats, Receptors, Drug, Structure-Activity Relationship, TRPV Cation Channels