116993-42-1Relevant articles and documents
Design and synthesis of orally available MEK inhibitors with potent in vivo antitumor efficacy
Adams, Mark E.,Wallace, Michael B.,Kanouni, Toufike,Scorah, Nicholas,O'Connell, Shawn M.,Miyake, Hiroshi,Shi, Lihong,Halkowycz, Petro,Zhang, Lilly,Dong, Qing
scheme or table, p. 2411 - 2414 (2012/05/05)
The structure-based design, synthesis, and biological evaluation of two novel series of potent and selective MEK kinase inhibitors are described herein. The elaboration of a lead pyrrole derivative to a bicyclic dihydroindolone core provided compounds wit
MEK INHIBITOR SALTS AND SOLVATES THEREOF
-
Page/Page column 14; 21, (2011/06/25)
The present invention relates to sodium salt forms of 7-(4-Bromo-2-fluoro- phenylamino)-6-methyl-5-oxo-1,3,5-tetrahydro-indolizine-8-carboxylic acid (2- hydroxyethoxy)-amide and 7-(4-Bromo-2-fluoro-phenylamino)-5-oxo- 1,2,3,5-tetrahydro- indolizine-8-carboxylic acid cyclopropylmethoxy-amide and their corresponding solvates and polymorphs, which are useful in the treatment of a disease, disorder or syndrome associated with MEK inhibition, such as cancer, in mammals.
MAPK/ERK KINASE INHIBITORS
-
Page/Page column 37; 38, (2009/05/28)
Compounds of the following formula are provided for use with MEK: wherein the variables are as defined herein. Also provided are pharmaceutical compositions, kits and articles of manufacture comprising such compounds; methods and intermediates useful for making the compounds; and methods of using said compounds.