Belyanskaya Svetlana L, Ding Yun, Callahan James F, Lazaar Aili L, Israel David I
GlaxoSmithKline R&D, 830 Winter Street, Waltham, MA, 02451, USA.
GlaxoSmithKline R&D, 709 Swedeland Road, King of Prussia, PA, 19406, USA.
Chembiochem. 2017 May 4;18(9):837-842. doi: 10.1002/cbic.201700014. Epub 2017 Mar 24.
DNA-encoded chemical library technology was developed with the vision of its becoming a transformational platform for drug discovery. The hope was that a new paradigm for the discovery of low-molecular-weight drugs would be enabled by combining the vast molecular diversity achievable with combinatorial chemistry, the information-encoding attributes of DNA, the power of molecular biology, and a streamlined selection-based discovery process. Here, we describe the discovery and early clinical development of GSK2256294, an inhibitor of soluble epoxide hydrolase (sEH, EPHX2), by using encoded-library technology (ELT). GSK2256294 is an orally bioavailable, potent and selective inhibitor of sEH that has a long half life and produced no serious adverse events in a first-time-in-human clinical study. To our knowledge, GSK2256294 is the first molecule discovered from this technology to enter human clinical testing and represents a realization of the vision that DNA-encoded chemical library technology can efficiently yield molecules with favorable properties that can be readily progressed into high-quality drugs.
DNA编码化学库技术的发展愿景是成为药物发现的变革性平台。人们希望,通过将组合化学可实现的巨大分子多样性、DNA的信息编码特性、分子生物学的力量以及基于筛选的简化发现过程相结合,能够开启一种发现低分子量药物的新范式。在此,我们描述了通过使用编码库技术(ELT)发现可溶性环氧化物水解酶(sEH,EPHX2)抑制剂GSK2256294及其早期临床开发情况。GSK2256294是一种口服生物可利用的、强效且选择性的sEH抑制剂,半衰期长,在首次人体临床研究中未产生严重不良事件。据我们所知,GSK2256294是从该技术中发现的首个进入人体临床试验的分子,代表了DNA编码化学库技术能够有效产生具有良好特性的分子,并可轻松推进成为高质量药物这一愿景的实现。