Yao Hong, Liu Junkai, Xu Shengtao, Zhu Zheying, Xu Jinyi
a State Key Laboratory of Natural Medicines and Department of Medicinal Chemistry , China Pharmaceutical University , Nanjing , P. R. China.
b Division of Molecular Therapeutics & Formulation, School of Pharmacy , The University of Nottingham , Nottingham , UK.
Expert Opin Drug Discov. 2017 Feb;12(2):121-140. doi: 10.1080/17460441.2016.1272757. Epub 2016 Dec 22.
Throughout history, natural products (NPs) have provided a rich source of compounds that have wide applications in the fields of medicine, health sciences, pharmacy and biology. Although naturally active substances are good lead compounds for the discovery of new drugs, most of them suffer from various deficiencies or shortcomings, such as complex structures, poor stability and solubility. Therefore, structural modification of NPs is needed to develop novel compounds with specific properties. Areas covered: This article presents an overview on the structural modifications of NPs in drug development. The application of multiple classes of NPs to the treatment of conditions such as cancers, infection, Alzheimer's and diabetes are discussed. This article also reveals that modification of NPs is a versatile approach to explore their mode of actions, which may lead to the discovery of novel drugs. Expert opinion: NPs are usually described by structural diversity and complexity. The use of isolated NPs as scaffolds for modification is a good approach to drug discovery and development. Despite many limitations associated with NPs, the total synthesis, semisynthetic modification, SAR-based modification, sometimes even a single atom alteration, may lead to the discovery of a novel drug.
纵观历史,天然产物(NPs)提供了丰富的化合物来源,这些化合物在医学、健康科学、药学和生物学领域有着广泛应用。尽管天然活性物质是发现新药的良好先导化合物,但它们大多存在各种缺陷或不足,如结构复杂、稳定性和溶解性差。因此,需要对天然产物进行结构修饰以开发具有特定性质的新型化合物。涵盖领域:本文概述了天然产物在药物开发中的结构修饰。讨论了多类天然产物在治疗癌症、感染、阿尔茨海默病和糖尿病等病症中的应用。本文还揭示,对天然产物进行修饰是探索其作用方式的一种通用方法,这可能会带来新药的发现。专家观点:天然产物通常以结构多样性和复杂性来描述。使用分离出的天然产物作为修饰支架是药物发现和开发的一种好方法。尽管天然产物存在许多局限性,但全合成、半合成修饰、基于构效关系的修饰,有时甚至是单个原子的改变,都可能带来新药的发现。