Stanway-Gordon Harriet A, Odger Jake A, Waring Michael J
Cancer Research Horizons Therapeutic Innovation, Chemistry, School of Natural and Environmental Sciences, Bedson Building, Newcastle University, Newcastle upon Tyne, NE1 7RU, United Kingdom.
Bioconjug Chem. 2023 Mar 8;34(4):756-63. doi: 10.1021/acs.bioconjchem.3c00051.
The capability of DNA encoded libraries (DELs) as a method of small molecule hit identification is becoming widely established in drug discovery. While their selection method offers advantages over more traditional means, DELs are limited by the chemistry that can be utilized to construct them. Significant advances in DNA compatible chemistry have been made over the past five years; however such procedures are still often burdened by substrate specificity and/or incomplete conversions, reducing the fidelity of the resulting libraries. One such reaction is the Heck coupling, for which current DNA-compatible protocols are somewhat unreliable. Utilizing micellar technology, we have developed a highly efficient DNA-compatible Heck reaction that proceeds on average to 95% conversion to product across a broad variety of structurally significant building blocks and multiple DNA conjugates. This work continues the application of micellar catalysis to the development of widely applicable, effective DNA-compatible reactions for use in DELs.
DNA编码文库(DELs)作为一种小分子命中识别方法,在药物发现中越来越得到广泛认可。虽然其筛选方法比更传统的方法具有优势,但DELs受到可用于构建它们的化学方法的限制。在过去五年中,与DNA兼容的化学取得了重大进展;然而,此类方法仍然常常受到底物特异性和/或不完全转化的困扰,降低了所得文库的保真度。Heck偶联反应就是其中之一,目前与DNA兼容的方案在一定程度上不可靠。利用胶束技术,我们开发了一种高效的与DNA兼容的Heck反应,该反应在各种结构上重要的构建块和多种DNA共轭物上平均能达到95%的产物转化率。这项工作继续将胶束催化应用于开发广泛适用、有效的与DNA兼容的反应,以用于DELs。