Bicyclic pyridinylpyrazoles of the formula (I)
in which the symbols have the meanings given in the description and agrochemically active salts thereof and their use for controlling unwanted microorganisms in crop protection and the protection of materials and for reducing mycotoxins in plants and plant parts, and also processes for preparing compounds of the formula (I).
Benzimidazoles and benzothiazoles as inhibitors of map kinase
申请人:Bonjouklian Rosanne
公开号:US20050272791A1
公开(公告)日:2005-12-08
The present invention provides kinase inhibitors of Formula I: wherein W represents inter alia imidazol, oxazol, pyrazol, thiazol as triazol, which are substituted by phenyl or thienyl. The disclosed compounds inhibit p-38 kinase and are useful in the treatment of metastasis or rheumatoid arthritis.
BENZIMIDAZOLES AND BENZOTHIAZOLES AS INHIBITORS OF MAP KINASE
申请人:ELI LILLY AND COMPANY
公开号:EP1554272A1
公开(公告)日:2005-07-20
BICYCLISCHE PYRIDINYLPYRAZOLE
申请人:Bayer Intellectual Property GmbH
公开号:EP2556073A1
公开(公告)日:2013-02-13
TGF-ß Inhibitors
申请人:Rigel Pharmaceuticals, Inc.
公开号:US20180086764A1
公开(公告)日:2018-03-29
Disclosed are pyrazole compounds, as well as pharmaceutical compositions and methods of use thereof. One embodiment is a compound having the structure and pharmaceutically acceptable salts, prodrugs and N-oxides thereof (and solvates and hydrates thereof), wherein A, X, Z, m, p, and R
2
are as described herein. In certain embodiments, a compound disclosed herein inhibits the activity of one or more members of the TGF-β superfamily, and can be used to treat disease by blocking such activity.