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用于表观遗传药物发现的聚焦文库:电子等排体的重要性。

Focused Libraries for Epigenetic Drug Discovery: The Importance of Isosteres.

作者信息

Green Adam I, Burslem George M

机构信息

Department of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States.

Department of Cancer Biology and Epigenetics Institute Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States.

出版信息

J Med Chem. 2021 Jun 10;64(11):7231-7240. doi: 10.1021/acs.jmedchem.1c00592. Epub 2021 May 27.

Abstract

Epigenetic drug discovery provides a wealth of opportunities for the discovery of new therapeutics but has been hampered by low hit rates, frequent identification of false-positives, and poor synthetic tractability. A key reason for this is that few screening collections consider the unique requirements of epigenetic targets despite significant medicinal chemistry interest. Here we analyze the suitability of some commercially available screening collections in the context of epigenetic drug discovery, with a particular focus on lysine post-translational modifications, and show that even privileged motifs found in U.S. Food and Drug Administration (FDA)-approved drugs are not present in these collections. We propose that the incorporation of epigenetic bioisosteres should become central in the design of new focused screening collections and highlight some opportunities for the development of synthetic methods which may improve the tractability of hit molecules.

摘要

表观遗传药物发现为新型治疗药物的发现提供了大量机会,但受到低命中率、频繁识别假阳性以及合成可处理性差的阻碍。造成这种情况的一个关键原因是,尽管有重大的药物化学研究兴趣,但很少有筛选库考虑到表观遗传靶点的独特要求。在这里,我们在表观遗传药物发现的背景下分析了一些市售筛选库的适用性,特别关注赖氨酸的翻译后修饰,并表明即使在美国食品药品监督管理局(FDA)批准的药物中发现的特权基序在这些库中也不存在。我们建议,表观遗传生物电子等排体的纳入应成为新的聚焦筛选库设计的核心,并强调一些合成方法开发的机会,这些机会可能会提高命中分子的可处理性。

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