Structure-based optimization of PKCθ inhibitors

被引:7
|
作者
Mosyak, L. [1 ]
Xu, Z. [1 ]
Joseph-McCarthy, D. [1 ]
Brooijmans, N. [1 ]
Somers, W. [1 ]
Chaudhary, D. [1 ]
机构
[1] Wyeth Ayerst Res, Cambridge, MA 02140 USA
关键词
ATP competitive kinase inhibitor; molecular modelling; protein kinase C (PKC); protein kinase C theta inhibitor; structure-based optimization; T-cell;
D O I
10.1042/BST0351027
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
PKC theta (protein kinase C theta) is a central signalling molecule in the T-cell receptor activation pathway and is a target for treatment of a number of diseases. Several PKC inhibitors are in the drug-discovery pharmaceutical programmes today for the treatment of cancer, diabetes and arthritis. CD4+ T-lymphocytes also play a critical role in the initiation and progression of allergic airway inflammation. our goal is the development of PKC theta antagonists as a means to control asthma and autoimmune diseases, using the strategy based on developing small-molecule agents that would block the enzyme's catalytic activity. Here, we discuss our work on the discovery of lead chemical series and review our X-ray structural and modelling approaches, including a structure-surrogate strategy that helped guide us in the lead compound optimizations.
引用
收藏
页码:1027 / 1031
页数:5
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