Radau Gregor, Gebel Jana, Rauh Daniel
Institute of Pharmacy, Ernst-Moritz-Arndt-University Greifswald, Pharmaceutical/Medicinal Chemistry, Friedrich-Ludwig-Jahn-Str. 17, D-17487 Greifswald, Germany.
Arch Pharm (Weinheim). 2003 Aug;336(8):372-80. doi: 10.1002/ardp.200300726.
Thrombosis is the result of defective regulation of the hemostasis system. This cardiovascular disorder may lead to deep vein thrombosis, myocardial infarction, and stroke. The majority of current drug research is focused on finding inhibitors of thrombin - the global player in hemostasis. In our work, we emphasize investigation of the marine environment to yield new lead structures from marine organisms like blue-green algae (cyanobacteria). This article deals with the design, syntheses, and inhibition tests of new low molecular weight thrombin inhibitors utilizing cyanopeptides, the secondary metabolites of cyanobacteria with interesting biological activities, as new lead structures. Starting with aeruginosin 98-B (2) as a lead structure, we have developed and synthesized new, selective acting inhibitors of thrombin (RA-1001 and RA-1002), which are suitable targets for further structure-activity studies.
血栓形成是止血系统调节缺陷的结果。这种心血管疾病可能导致深静脉血栓形成、心肌梗死和中风。目前大多数药物研究都集中在寻找凝血酶抑制剂上——凝血酶是止血过程中的关键因子。在我们的工作中,我们着重研究海洋环境,以便从蓝藻(蓝细菌)等海洋生物中获取新的先导结构。本文论述了利用蓝藻肽(蓝细菌具有有趣生物活性的次生代谢产物)作为新的先导结构,设计、合成新型低分子量凝血酶抑制剂并进行抑制试验。以铜绿假单胞菌素98-B(2)作为先导结构,我们开发并合成了新型、具有选择性作用的凝血酶抑制剂(RA-1001和RA-1002),它们是进一步进行构效关系研究的合适靶点。