Amgen, Inc., Department of Medicinal Chemistry, Cambridge, Massachusetts 02142, USA.
Expert Opin Ther Pat. 2010 Nov;20(11):1573-93. doi: 10.1517/13543776.2010.517749. Epub 2010 Sep 10.
Lck (p56(lck) or lymphocyte specific kinase) is a cytoplasmic tyrosine kinase of the Src family expressed in T cells and natural killer (NK) cells. Genetic evidence from knockout mice and human mutations demonstrates that Lck kinase activity is critical for T cell receptor (TCR)-mediated signaling, leading to normal T-cell development and activation. Selective inhibition of Lck is expected to offer a new therapy for the treatment of T-cell-mediated autoimmune and inflammatory disorders and/or organ transplant rejection.
This review covers the patents, patent applications and associated publications for small molecule kinase inhibitors of Lck since 2005 and attempts to place them in context from a structural point of view.
Readers will gain an overview of the structural classes and binding modes of Lck inhibitors, the major players in this area and an insight into the current state of the field.
The search for a potent and orally active inhibitor of Lck has been an intense area of research for a number of years. Despite tremendous efforts, the identification of a highly selective and potent Lck inhibitor suitable for use as an immunosuppressive agent remains elusive.
Lck(p56(lck)或淋巴细胞特异性激酶)是Src 家族的细胞质酪氨酸激酶,在 T 细胞和自然杀伤(NK)细胞中表达。来自敲除小鼠的遗传证据和人类突变表明,Lck 激酶活性对于 T 细胞受体(TCR)介导的信号转导至关重要,导致正常的 T 细胞发育和激活。选择性抑制 Lck 有望为治疗 T 细胞介导的自身免疫和炎症性疾病和/或器官移植排斥提供新的治疗方法。
本综述涵盖了 2005 年以来小分子 Lck 激酶抑制剂的专利、专利申请和相关出版物,并尝试从结构角度对其进行阐述。
读者将获得 Lck 抑制剂的结构类别和结合模式、该领域的主要参与者的概述,并深入了解该领域的现状。
多年来,寻找一种有效且口服活性的 Lck 抑制剂一直是一个激烈的研究领域。尽管付出了巨大的努力,但仍然难以确定一种高度选择性和有效的 Lck 抑制剂,适用于作为免疫抑制剂。