Novel quinazolinamide derivatives of the formula (I), in which R
1
-R
3
have the meanings indicated in Claim
1,
are HSP90 inhibitors and can be used for the preparation of a medicament for the treatment of diseases in which the inhibition, regulation and/or modulation of HSP90 plays a role.
The present invention provides aldosterone synthase inhibitors of the formula:
intermediates, methods for their preparation, pharmaceutical preparations, and methods for their use.
这项发明提供了以下结构的醛固酮合成酶抑制剂:
中间体,其制备方法,药物制剂以及使用方法。
INDAZOLONE ANALOGS AS GLYCOGEN SYNTHASE ACTIVATORS
申请人:Bolin David Robert
公开号:US20110112147A1
公开(公告)日:2011-05-12
Provided herein are compounds of the formula (I):
as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of metabolic diseases and disorders such as, for example, type II diabetes mellitus.
[EN] OXADIAZOLE MODULATORS OF S1P METHODS OF MAKING AND USING<br/>[FR] MODULATEURS D'OXADIAZOLE DE S1P, AINSI QUE PROCÉDÉS DE FABRICATION ET D'UTILISATION CORRESPONDANTS
申请人:EXELIXIS INC
公开号:WO2017004608A1
公开(公告)日:2017-01-05
The invention is directed to Compounds of Formula (I): wherein each variable is defined herein, as well as methods of making and using the compounds as agonists of S1P1 and/or S1P5 for instance for treating graft versus host disease and autoimmune diseases.