| Literature DB >> 24900312 |
Hiroyuki Abe1, Shinichi Kikuchi1, Kazuhide Hayakawa1, Tetsuya Iida1, Noboru Nagahashi1, Katsuya Maeda1, Johei Sakamoto1, Noriaki Matsumoto1, Tomoya Miura1, Koji Matsumura1, Noriyoshi Seki1, Takashi Inaba1, Hisashi Kawasaki1, Takayuki Yamaguchi1, Reina Kakefuda1, Toyomichi Nanayama1, Hironori Kurachi1, Yoshikazu Hori1, Takayuki Yoshida2, Junya Kakegawa2, Yoshihiro Watanabe2, Aidan G Gilmartin3, Mark C Richter3, Katherine G Moss3, Sylvie G Laquerre3.
Abstract
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.Entities:
Keywords: GSK1120212; JTP-74057; MEK inhibitor; antiproliferative
Year: 2011 PMID: 24900312 PMCID: PMC4018163 DOI: 10.1021/ml200004g
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345