1 EU-OPENSCREEN, Leibniz Research Institute for Molecular Pharmacology, Berlin, Germany.
2 Organic Synthesis Methodology Group, Latvian Institute of Organic Synthesis, Riga, Latvia.
SLAS Discov. 2019 Mar;24(3):398-413. doi: 10.1177/2472555218816276. Epub 2019 Jan 7.
Compound screening in biological assays and subsequent optimization of hits is indispensable for the development of new molecular research tools and drug candidates. To facilitate such discoveries, the European Research Infrastructure EU-OPENSCREEN was founded recently with the support of its member countries and the European Commission. Its distributed character harnesses complementary knowledge, expertise, and instrumentation in the discipline of chemical biology from 20 European partners, and its open working model ensures that academia and industry can readily access EU-OPENSCREEN's compound collection, equipment, and generated data. To demonstrate the power of this collaborative approach, this perspective article highlights recent projects from EU-OPENSCREEN partner institutions. These studies yielded (1) 2-aminoquinazolin-4(3 H)-ones as potential lead structures for new antimalarial drugs, (2) a novel lipodepsipeptide specifically inducing apoptosis in cells deficient for the pVHL tumor suppressor, (3) small-molecule-based ROCK inhibitors that induce definitive endoderm formation and can potentially be used for regenerative medicine, (4) potential pharmacological chaperones for inborn errors of metabolism and a familiar form of acute myeloid leukemia (AML), and (5) novel tankyrase inhibitors that entered a lead-to-candidate program. Collectively, these findings highlight the benefits of small-molecule screening, the plethora of assay designs, and the close connection between screening and medicinal chemistry within EU-OPENSCREEN.
化合物筛选在生物测定中以及随后对命中化合物的优化对于开发新的分子研究工具和药物候选物是不可或缺的。为了促进这些发现,在其成员国和欧盟委员会的支持下,最近成立了一个名为 EU-OPENSCREEN 的欧洲研究基础设施。它的分布式特性利用了 20 个欧洲合作伙伴在化学生物学领域的互补知识、专业知识和仪器设备,其开放的工作模式确保了学术界和工业界可以方便地使用 EU-OPENSCREEN 的化合物库、设备和生成的数据。为了展示这种协作方法的威力,本文重点介绍了 EU-OPENSCREEN 合作伙伴机构的最新项目。这些研究产生了(1)2-氨基喹唑啉-4(3 H)-酮类化合物,作为新型抗疟药物的潜在先导结构,(2)一种新型脂肽,可特异性诱导 pVHL 肿瘤抑制因子缺失的细胞凋亡,(3)基于小分子的 ROCK 抑制剂,可诱导确定性内胚层形成,可潜在用于再生医学,(4)代谢性遗传病和急性髓系白血病(AML)的潜在药理学伴侣,以及(5)进入先导候选药物计划的新型 Tankyrase 抑制剂。总的来说,这些发现强调了小分子筛选、大量测定设计以及 EU-OPENSCREEN 内筛选和药物化学之间的紧密联系的优势。