Substituted Quinazoline and Pyridopyrimidine Derivatives Useful as Anticancer Agents
申请人:PFIZER INC.
公开号:US20190233440A1
公开(公告)日:2019-08-01
Compounds of the general formula:
processes for the preparation of these compounds, compositions containing these compounds, and the uses of these compounds.
具有通用公式:
这些化合物的制备方法,包含这些化合物的组合物,以及这些化合物的用途。
[EN] KRAS G12D INHIBITORS<br/>[FR] INHIBITEURS DE KRAS G12D
申请人:MIRATI THERAPEUTICS INC
公开号:WO2021041671A1
公开(公告)日:2021-03-04
The present invention relates to compounds that inhibit KRas G12D. In particular, the present invention relates to compounds that inhibit the activity of KRas G12D, pharmaceutical compositions comprising the compounds and methods of use therefor.
APOPTOSIS INDUCING AGENTS FOR THE TREATMENT OF CANCER AND IMMUNE AND AUTOIMMUNE DISEASES
申请人:Bruncko Milan
公开号:US20100305122A1
公开(公告)日:2010-12-02
Disclosed are compounds which inhibit the activity of anti-apoptotic Bcl-2 proteins, compositions containing the compounds and methods of treating diseases during which is expressed anti-apoptotic Bcl-2 protein.
[EN] PIPERAZINE DERIVATIVES AND THEIR USE AS KIT MODULATORS<br/>[FR] DÉRIVÉS DE PIPÉRAZINE ET LEUR UTILISATION COMME MODULATEURS DE KIT
申请人:BLUEPRINT MEDICINES CORP
公开号:WO2014160521A1
公开(公告)日:2014-10-02
Compounds having structural formula (I) : or a pharmaceutically acceptable salt or a tautomer thereof or having structural formula (III) : or a pharmaceutically acceptable salt or tautomer thereof useful for treating disorders related to Kit are described herein.
MELT-EXTRUDED SOLID DISPERSIONS CONTAINING AN APOPTOSIS-INDUCING AGENT
申请人:Birtalan Esther
公开号:US20120108590A1
公开(公告)日:2012-05-03
A pro-apoptotic solid dispersion comprises, in essentially non-crystalline form, a Bcl-2 family protein inhibitory compound of Formula I as defined herein, dispersed in a solid matrix that comprises (a) a pharmaceutically acceptable water-soluble polymeric carrier and (b) a pharmaceutically acceptable surfactant. A process for preparing such a solid dispersion comprises subjecting to elevated temperature the compound of Formula I, the water-soluble polymeric carrier and the surfactant, to provide an extrudable semi-solid mixture; extruding the semi-solid mixture; and cooling the resulting extrudate to to provide a solid matrix comprising the polymeric carrier and the surfactant and having the compound dispersed in essentially non-crystalline form therein. The solid dispersion is suitable for oral administration to a subject in need thereof for treatment of a disease characterized by overexpression of one or more anti-apoptotic Bcl-2 family proteins, for example cancer or an immune or autoimmune disease.