Feng Yangbo, LoGrasso Philip V
Translational Research Institute, The Scripps Research Institute , Scripps Florida, #2A1, 130 Scripps Way, Jupiter, FL 33458 , USA +1 561 228 2201 ;
Expert Opin Ther Pat. 2014 Mar;24(3):295-307. doi: 10.1517/13543776.2014.863279. Epub 2013 Nov 27.
The Rho kinase/ROCK is critical in vital signal transduction pathways central to many essential cellular activities. Since ROCK possess multiple substrates, modulation of ROCK activity is useful for treatment of many diseases.
Significant progress has been made in the development of ROCK inhibitors over the past two years (Jan 2012 to Aug 2013). Patent search in this review was based on FPO IP Research and Communities and Espacenet Patent Search. In this review, patent applications will be classified into four groups for discussions. The grouping is mainly based on structures or scaffolds (groups 1 and 2) and biological functions of ROCK inhibitors (groups 3 and 4). These four groups are i) ROCK inhibitors based on classical structural elements for ROCK inhibition; ii) ROCK inhibitors based on new scaffolds; iii) bis-functional ROCK inhibitors; and iv) novel applications of ROCK inhibitors.
Although currently only one ROCK inhibitor (fasudil) is used as a drug, more drugs based on ROCK inhibition are expected to be advanced into market in the near future. Several directions should be considered for future development of ROCK inhibitors, such as soft ROCK inhibitors, bis-functional ROCK inhibitors, ROCK2 isoform-selective inhibitors, and ROCK inhibitors as antiproliferation agents.
Rho激酶/ROCK在许多重要细胞活动所依赖的关键信号转导通路中起着至关重要的作用。由于ROCK有多种底物,调节ROCK活性对多种疾病的治疗有用。
在过去两年(2012年1月至2013年8月)中,ROCK抑制剂的研发取得了重大进展。本综述中的专利检索基于FPO IP研究与社区以及欧洲专利局专利检索。在本综述中,专利申请将分为四组进行讨论。分组主要基于ROCK抑制剂的结构或骨架(第1组和第2组)以及生物学功能(第3组和第4组)。这四组分别是:i)基于经典结构元件的ROCK抑制剂;ii)基于新骨架的ROCK抑制剂;iii)双功能ROCK抑制剂;iv)ROCK抑制剂的新应用。
尽管目前仅有一种ROCK抑制剂(法舒地尔)作为药物使用,但预计在不久的将来会有更多基于ROCK抑制的药物进入市场。ROCK抑制剂的未来发展应考虑几个方向,如软性ROCK抑制剂、双功能ROCK抑制剂、ROCK2亚型选择性抑制剂以及作为抗增殖剂的ROCK抑制剂。