Key points are not available for this paper at this time.
A series of N-pyridyl benzamide KCNQ2/Q3 potassium channel openers were identified and found to be active in animal models of epilepsy and pain. The best compound 12 ICA-027243, N-(6-chloro-pyridin-3-yl)-3,4-difluoro-benzamide has an EC50 of 0.38 μM and is selective for KCNQ2/Q3 channels. This compound was active in several rodent models of epilepsy and pain but upon repeated dosing had a number of unacceptable toxicities that prevented further development. On the basis of the structure-activity relationships developed around 12, a second compound, 51, N-(2-chloro-pyrimidin-5-yl)-3,4-difluoro-benzamide, ICA-069673, was prepared and advanced into a phase 1 clinical study. Herein, we describe the structure-activity relationships that led to the identification of compound 12 and to the corresponding pyrimidine 51.
Amato et al. (Thu,) studied this question.