Crude extractchemical engineering: strategy for the library generation of novel bio-active chemical entities

IF 7.3 2区 生物学 Q1 PLANT SCIENCES Phytochemistry Reviews Pub Date : 2024-08-12 DOI:10.1007/s11101-024-10009-1
Jyoti Pal, Varsha Chauhan, Manu Sharma
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Abstract

The natural origin secondary metabolites have been considered as one of the richest source of new chemical entities with vast array of structural diversity and complexity. The natural compounds have played significant and crucial part in the development of number of therapeutic agents for various diseases especially in the cancer and infectious disease segment. The vast structural and molecular diversity of chemicals present in natural sources inspired medicinal chemist from ages to explore the chemotypes for the innovation and design of new pharmaceuticals and chemical entities. The design of diverse libraries of natural product congeners or derivatives can be achieved using various approaches and strategies to expand the natural product frameworks. Modifying common reactive molecular fragments in natural extracts is an effective strategy for creating pharmacologically active compounds. Various extraction and purification techniques, such as high performance liquid chromatography and supercritical fluid extraction along with membrane-based technologies, are employed to isolate these bioactive compounds.Direct crude extract modification of natural products is an interesting and recent strategy to evolve new chemical entities with diversity in structure and pharmacophore. The reactive chemical moieties present in most of the natural products can be engineered chemically by treating them with particular reagents to yield chemically modified extracts or semi-synthetic molecules constituting distinct libraries with enhanced chemo-diversity and improved pharmacology. This review aims to present latest developments in the synthesis of natural product-inspired medicinal compound libraries via direct chemical modification of crude extracts.

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粗提物化学工程:新型生物活性化学实体库生成策略
天然次生代谢物被认为是新化学实体的最丰富来源之一,具有结构多样性和复杂性。天然化合物在开发治疗各种疾病(尤其是癌症和传染病)的药物方面发挥了重要作用。天然来源中存在的化学物质在结构和分子上的多样性,激励着药物化学家从古至今不断探索化学类型,以创新和设计新的药物和化学实体。设计天然产物同系物或衍生物的多样化文库,可以采用各种方法和策略来扩展天然产物框架。对天然提取物中常见的活性分子片段进行修饰,是创造药理活性化合物的有效策略。直接对天然产物的粗提取物进行修饰是一种有趣的新策略,可使新的化学实体在结构和药理上具有多样性。大多数天然产物中的活性化学分子都可以用特定的试剂进行化学工程处理,从而获得化学修饰的提取物或半合成分子,构成具有更强化学多样性和更好药理作用的独特化合物库。本综述旨在介绍通过直接对粗提取物进行化学修饰来合成受天然产物启发的药用化合物库的最新进展。
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来源期刊
Phytochemistry Reviews
Phytochemistry Reviews PLANT SCIENCES-
CiteScore
16.30
自引率
2.60%
发文量
54
审稿时长
2 months
期刊介绍: Phytochemistry Reviews is the sole review journal encompassing all facets of phytochemistry. It publishes peer-reviewed papers in six issues annually, including topical issues often stemming from meetings organized by the Phytochemical Society of Europe. Additionally, the journal welcomes original review papers that contribute to advancing knowledge in various aspects of plant chemistry, function, biosynthesis, effects on plant and animal physiology, pathology, and their application in agriculture and industry. Invited meeting papers are supplemented with additional review papers, providing a comprehensive overview of the current status across all areas of phytochemistry.
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