化学
激酶
蛋白激酶A
MAPK/ERK通路
效力
磷酸化
丝裂原活化蛋白激酶
IC50型
癌症研究
药理学
体外
生物化学
医学
作者
Eli M. Wallace,Joseph P. Lyssikatos,James F. Blake,Jeongbeob Seo,Hong Woon Yang,Tammie C. Yeh,Michele Perrier,Heidi Jarski,Vivienne Marsh,G Pöch,Michelle Goyette Livingston,Jennifer Otten,Gary P. Hingorani,Rich Woessner,Patrice Lee,James D. Winkler,Kevin M. Koch
摘要
The role of MEK 1,2 in cancer tumorgenesis has been clearly demonstrated preclinically, and two selective inhibitors are currently undergoing clinical evaluation to determine their role in the human disease. We have discovered 4-(4-bromo-2-fluorophenylamino)-1-methylpyridin-2(1H)-ones as a new class of ATP noncompetitive MEK inhibitors. These inhibitors exhibit excellent cellular potency and good pharmacokinetic properties and have demonstrated the ability to inhibit ERK phosphorylation in HT-29 tumors from mouse xenograft studies.
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