[EN] NITROGEN CONTAINING HETEROCYCLIC COMPOUNDS AS PIK3 -DELTA INHIBITORS [FR] COMPOSÉS HÉTÉROCYCLIQUES CONTENANT DE L'AZOTE COMME INHIBITEURS DE PI3K-DELTA
[EN] COMPOSITIONS AND THERAPEUTIC USES OF IKK-RELATED KINASE EPSILON AND TANKBINDING KINASE 1 INHIBITORS<br/>[FR] COMPOSITIONS ET UTILISATIONS THÉRAPEUTIQUES D'INHIBITEURS DE LA KINASE EPSILON LIÉE À IKK ET DE LA KINASE 1 DE LIAISON À TANK
申请人:MYREXIS INC
公开号:WO2012142329A1
公开(公告)日:2012-10-18
The invention relates to compounds, pharmaceutical compositions and medicaments comprising such compounds, and the use of these compounds, compositions, and medicaments in methods of treating diseases and disorders.
Compounds of the formula I, in which R
1
, R
2
, X and Y have the meanings indicated in Claim
1
, are inhibitors of TBK1 and IKKε and can be employed, inter alia, for the treatment of cancer and inflammatory diseases.
COMPOSITIONS AND THERAPEUTIC USES OF IKK-RELATED KINASE EPSILON AND TANKBINDING KINASE 1 INHIBITORS
申请人:Holcomb Ryan
公开号:US20140288044A1
公开(公告)日:2014-09-25
The invention relates to compounds, pharmaceutical compositions and medicaments comprising such compounds, and the use of these compounds, compositions, and medicaments in methods of treating diseases and disorders.
A process for preparing a compound of formula:
wherein R3 is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, alkoxy, amido, amino, alkoxycarbonyl sulfonamido, halo, cyano, hydroxy or nitro, comprising reacting a compound of formula:
with a compound of formula:
in the presence of a base. The THP group may be removed with acid to make chemical entities that modulate PI3 kinase activity for treating diseases and conditions associated with PI3 kinase activity and/or formulated into pharmaceutical compositions containing such chemical entities.
A PHARMACEUTICAL COMPOSITION FOR ORAL ADMINISTRATION
申请人:Intellikine, LLC
公开号:EP3441392A1
公开(公告)日:2019-02-13
A pharmaceutical composition for oral administration comprising an effective amount of a compound of Formula V-A2:
or a pharmaceutically acceptable salt thereof;
wherein B is a moiety of Formula II:
Wc is aryl, heteroaryl, heterocycloalkyl, or cycloalkyl;
q is an integer of 0 or 1;
R1 is hydrogen, alkyl, or halo;
R2 is alkyl or halo;
R3 is halo; and
R9 is alkyl, or heterocycloalkyl;
and one or more pharmaceutically acceptable excipients suitable for oral administration. The pharmaceutical composition may contain an effective amount of a second agent such as a chemotherapeutic agent, e.g. a proteasome inhibitor, an alkylating agent or a therapeutic antibody.