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大环化合物在药物化学中的设计、性质及近期应用

Design, Properties and Recent Application of Macrocycles in Medicinal Chemistry.

作者信息

Ermert Philipp

机构信息

Polyphor Ltd Hegenheimermattweg 125 CH-4123 Allschwil;, Email:

出版信息

Chimia (Aarau). 2017 Oct 25;71(10):678-702. doi: 10.2533/chimia.2017.678.

Abstract

Macrocyclic compounds have recently received increasing attention in drug discovery as these compounds offer the potential to modulate difficult targets and to access novel chemotypes. Approaches towards libraries of macrocyclic compounds based on modular organic synthesis and applications of these technology platforms to find and improve biologically active compounds are introduced in this minireview. Alternatively, lead compounds may be obtained by truncation and modification of macrocyclic natural products. Selected medicinal chemistry programs are discussed, illustrating a macrocyclization approach toward ligands with improved properties. The design of such ligands is often informed by X-ray crystal structures of protein-ligand complexes. Efforts to understand cellular permeability and oral bioavailability of cyclic peptides and non-peptidic macrocycles are summarized.

摘要

大环化合物最近在药物研发中受到越来越多的关注,因为这些化合物具有调节难以靶向的靶点以及获得新型化学结构类型的潜力。本综述介绍了基于模块化有机合成构建大环化合物库的方法,以及这些技术平台在发现和优化生物活性化合物方面的应用。此外,先导化合物也可通过大环天然产物的截短和修饰获得。文中讨论了一些选定的药物化学项目,展示了一种用于改进配体性质的大环化方法。此类配体的设计通常受蛋白质 - 配体复合物的X射线晶体结构的启发。文中还总结了对环肽和非肽大环化合物的细胞通透性和口服生物利用度的研究成果。

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