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Updated: Jun 7, 2026

07:49
Characterize Disease-related Mutants of RAF Family Kinases by Using a Set of Practical and Feasible Methods
Published on: July 17, 2019
Indazolylpyrazolopyrimidine as highly potent B-Raf inhibitors with in vivo activity
Xiaolun Wang1, Dan M Berger, Edward J Salaski
1Pfizer Global Research and Development, 401 N Middletown Road, Pearl River, New York 10965, United States. xxw104@gmail.com
Journal of Medicinal Chemistry
|October 22, 2010
Abstract:
Novel indazolylpyrazolo[1,5-a]pyrimidine analogues have been prepared and found to be extremely potent type I B-Raf inhibitors. The lead compound shows good selectivity against a panel of 60 kinases, possesses a desirable pharmacokinetic profile, and demonstrates excellent in vivo antitumor efficacy in B-Raf mutant xenograft models.

