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
相关论文
共 50 条
  • [21] Structure-based optimization of non-peptidic Cathepsin D inhibitors
    Graedler, Ulrich
    Czodrowski, Paul
    Tsaklakidis, Christos
    Klein, Markus
    Werkmann, Daniela
    Lindemann, Sven
    Maskos, Klaus
    Leuthner, Birgitta
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2014, 24 (17) : 4141 - 4150
  • [22] NMR structure-based optimization of Staphylococcus aureus sortase A pyridazinone inhibitors
    Chan, Albert H.
    Yi, Sung Wook
    Weiner, Ethan M.
    Amer, Brendan R.
    Sue, Christopher K.
    Wereszczynski, Jeff
    Dillen, Carly A.
    Senese, Silvia
    Torres, Jorge Z.
    McCammon, J. Andrew
    Miller, Lloyd S.
    Jung, Michael E.
    Clubb, Robert T.
    CHEMICAL BIOLOGY & DRUG DESIGN, 2017, 90 (03) : 327 - 344
  • [23] Discovery of selective BPTF bromodomain inhibitors by screening and structure-based optimization
    Xiong, Liang
    Mao, Xin
    Guo, Yinping
    Zhou, Yangli
    Chen, Mingxin
    Chen, Pei
    Yang, Shengyong
    Li, Linli
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2021, 545 : 125 - 131
  • [24] Structure-based design and combinatorial optimization of novel thymidylate synthase inhibitors
    Tondi, D
    Slomczynska, U
    Ghelli, S
    Watterson, DN
    Costi, MP
    Shoichet, BK
    FASEB JOURNAL, 1997, 11 (09): : A837 - A837
  • [25] Structure-based optimization of phenylbutyrate-derived histone deacetylase inhibitors
    Lu, Q
    Wang, DS
    Chen, CS
    Hu, YD
    Chen, CS
    JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (17) : 5530 - 5535
  • [26] Structure-based inhibitors of tau aggregation
    Seidler, P. M.
    Boyer, D. R.
    Rodriguez, J. A.
    Sawaya, M. R.
    Cascio, D.
    Murray, K.
    Gonen, T.
    Eisenberg, D. S.
    NATURE CHEMISTRY, 2018, 10 (02) : 170 - 176
  • [27] Structure-based development of PDEδ inhibitors
    Martin-Gago, Pablo
    Fansa, Eyad Kalawy
    Wittinghofer, Alfred
    Waldmann, Herbert
    BIOLOGICAL CHEMISTRY, 2017, 398 (5-6) : 535 - 545
  • [28] Structure-based design of thrombin inhibitors
    Pfau, R
    CURRENT OPINION IN DRUG DISCOVERY & DEVELOPMENT, 2003, 6 (04) : 437 - 450
  • [29] Structure-Based Design of Ricin Inhibitors
    Jasheway, Karl
    Pruet, Jeffrey
    Anslyn, Eric V.
    Robertus, Jon D.
    TOXINS, 2011, 3 (10): : 1233 - 1248
  • [30] Structure-based inhibitors of tau aggregation
    P. M. Seidler
    D. R. Boyer
    J. A. Rodriguez
    M. R. Sawaya
    D. Cascio
    K. Murray
    T. Gonen
    D. S. Eisenberg
    Nature Chemistry, 2018, 10 (2) : 170 - 176