Article
Two classes of structurally different antagonists display similar species preference for the human tachykinin neurokinin3 receptor.
Molecular pharmacology - 1 Oct 1995
Chung F Z, Wu L H, Tian Y, Vartanian M A, Lee H, Bikker J, Humblet C, Pritchard M C, Raphy J, Suman-Chauhan N
Abstract excerpt
Two classes of structurally different tachykinin neurokinin3 (NK3) antagonists were used to evaluate species difference in antagonist binding between human and rat NK3 receptors. In competition binding experiments with [125I-MePhe7]NKB as radioligand, PD 154740, PD 157672, SR 48968, and SR 142801 displayed lower Ki values for the human NK3 receptor (40 +/- 4, 12 +/- 1,350 +/- 50, and 0.40 +/- 0.05 nM,...
Topics
- Animals
- Benzamides
- Binding, Competitive
- CHO Cells
- Cricetinae
- Dipeptides
- Humans
- Inositol Phosphates
- Iodine Radioisotopes
- Kinetics
- Mutation
