激酶
MEK抑制剂
MAPK/ERK通路
药物发现
化学
蛋白激酶A
药理学
细胞外信号调节激酶
乙酰胺
药品
虚拟筛选
医学
生物化学
有机化学
作者
Hiroyuki Abé,Shinichi Kikuchi,Kazuhide Hayakawa,Tetsuya Iida,Noboru Nagahashi,Katsuya Maeda,Johei Sakamoto,Noriaki Matsumoto,Tomoya Miura,Koji Matsumura,Noriyoshi Seki,Takashi Inaba,Hisashi Kawasaki,Takayuki Yamaguchi,Reina Kakefuda,Toyomichi Nanayama,Hironori Kurachi,Yoshikazu Hori,Takayuki Yoshida,Junya Kakegawa
摘要
Inhibition of mitogen-activated protein kinase/extracellular signal-regulated kinase kinase (MEK) represents a promising strategy for the discovery of a new generation of anticancer chemotherapeutics. Our synthetic efforts, beginning from the lead compound 2, were directed at improving antiproliferative activity against cancer cells as well as various drug properties. These efforts led to the discovery of N-{3-[3-cyclopropyl-5-(2-fluoro-4-iodophenylamino)-6,8-dimethyl-2,4,7-trioxo-3,4,6,7-tetrahydro-2H-pyrido[4,3-d]pyrimidin-1-yl]phenyl}acetamide dimethylsulfoxide solvate (GSK1120212, JTP-74057 DMSO solvate; 1), a selective and highly potent MEK inhibitor with improved drug properties. We further confirmed that the antiproliferative activity correlates with cellular MEK inhibition and observed significant antitumor activity with daily oral dosing of 1 in a tumor xenograft model. These qualities led to the selection of 1 for clinical development.
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