Isidro-Llobet Albert, Hadje Georgiou Kathy, Galloway Warren R J D, Giacomini Elisa, Hansen Mette R, Méndez-Abt Gabriela, Tan Yaw Sing, Carro Laura, Sore Hannah F, Spring David R
Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK.
Org Biomol Chem. 2015 Apr 21;13(15):4570-80. doi: 10.1039/c5ob00371g.
Macrocyclic peptidomimetics are associated with a broad range of biological activities. However, despite such potentially valuable properties, the macrocyclic peptidomimetic structural class is generally considered as being poorly explored within drug discovery. This has been attributed to the lack of general methods for producing collections of macrocyclic peptidomimetics with high levels of structural, and thus shape, diversity. In particular, there is a lack of scaffold diversity in current macrocyclic peptidomimetic libraries; indeed, the efficient construction of diverse molecular scaffolds presents a formidable general challenge to the synthetic chemist. Herein we describe a new, advanced strategy for the diversity-oriented synthesis (DOS) of macrocyclic peptidomimetics that enables the combinatorial variation of molecular scaffolds (core macrocyclic ring architectures). The generality and robustness of this DOS strategy is demonstrated by the step-efficient synthesis of a structurally diverse library of over 200 macrocyclic peptidomimetic compounds, each based around a distinct molecular scaffold and isolated in milligram quantities, from readily available building-blocks. To the best of our knowledge this represents an unprecedented level of scaffold diversity in a synthetically derived library of macrocyclic peptidomimetics. Cheminformatic analysis indicated that the library compounds access regions of chemical space that are distinct from those addressed by top-selling brand-name drugs and macrocyclic natural products, illustrating the value of our DOS approach to sample regions of chemical space underexploited in current drug discovery efforts. An analysis of three-dimensional molecular shapes illustrated that the DOS library has a relatively high level of shape diversity.
大环肽模拟物具有广泛的生物活性。然而,尽管具有这些潜在的宝贵特性,但在药物发现领域,大环肽模拟物结构类别通常被认为尚未得到充分探索。这归因于缺乏用于生成具有高水平结构多样性(进而形状多样性)的大环肽模拟物集合的通用方法。特别是,当前的大环肽模拟物文库缺乏支架多样性;事实上,高效构建多样的分子支架对合成化学家来说是一个巨大的普遍挑战。在此,我们描述了一种用于大环肽模拟物的多样性导向合成(DOS)的新的先进策略,该策略能够实现分子支架(核心大环环结构)的组合变化。通过从容易获得的构建模块高效合成一个包含200多种大环肽模拟物化合物的结构多样的文库,每个化合物都基于一个独特的分子支架并以毫克量分离,证明了这种DOS策略的通用性和稳健性。据我们所知,这代表了合成衍生的大环肽模拟物文库中前所未有的支架多样性水平。化学信息学分析表明,文库化合物进入的化学空间区域与畅销品牌药物和大环天然产物所涉及的区域不同,这说明了我们的DOS方法在当前药物发现工作中对未充分开发的化学空间区域进行采样的价值。对三维分子形状的分析表明,DOS文库具有相对较高水平的形状多样性。