206190-25-2Relevant articles and documents
Discovery of a first-in-class receptor interacting protein 2 (RIP2) kinase specific clinical candidate, 2-((4-(Benzo[ d]thiazol-5-ylamino)-6-(tert-butylsulfonyl)quinazolin-7-yl)oxy)ethyl dihydrogen phosphate, for the treatment of inflammatory diseases
Haile, Pamela A.,Casillas, Linda N.,Votta, Bartholomew J.,Wang, Gren Z.,Charnley, Adam K.,Dong, Xiaoyang,Bury, Michael J.,Romano, Joseph J.,Mehlmann, John F.,King, Bryan W.,Erhard, Karl F.,Hanning, Charles R.,Lipshutz, David B.,Desai, Biva M.,Capriotti, Carol A.,Schaeffer, Michelle C.,Berger, Scott B.,Mahajan, Mukesh K.,Reilly, Michael A.,Nagilla, Rakesh,Rivera, Elizabeth J.,Sun, Helen H.,Kenna, John K.,Beal, Allison M.,Ouellette, Michael T.,Kelly, Mike,Stemp, Gillian,Convery, Maíre A.,Vossenk?mper, Anna,Macdonald, Thomas T.,Gough, Peter J.,Bertin, John,Marquis, Robert W.
, p. 6482 - 6494 (2019/08/20)
RIP2 kinase has been identified as a key signal transduction partner in the NOD2 pathway contributing to a variety of human pathologies, including immune-mediated inflammatory diseases. Small-molecule inhibitors of RIP2 kinase or its signaling partners on
PRODRUGS OF AMINO QUINAZOLINE KINASE INHIBITOR
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Page/Page column 31, (2014/04/03)
Disclosed are compounds having Formula (I); wherein X is as defined herein, and methods of making and using the same.
4-aminoquinazolone derivatives
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, (2008/06/13)
This invention relates to certain 4-aminoquinazoline derivatives of the formula and their pharmaceutically acceptable salts wherein R1, Q1, m, n, and Z are defined as in the specification. The compounds of formula I and pharmaceutically acceptable salts are useful for the treatment of hyperproliferative disorders and conditions in mammals.