Empowering molecular complexity via biocatalysis: emerging blueprints in the total synthesis of medicinally relevant natural products

IF 3.597 Q2 Pharmacology, Toxicology and Pharmaceutics
MedChemComm Pub Date : 2026-02-23 DOI:10.1039/D5MD01011J
Ram N. Yadav, Sovan Dey, Md. Firoj Hossain, Devalina Ray, Bimal K. Banik, Luciana C. Schmidt and Vandana Singh
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引用次数: 0

Abstract

Biocatalysis has ascended as a defining force in contemporary total synthesis, furnishing catalytic modalities that deliver molecular complexity with unparalleled chemo-, regio-, and stereo-control. As structurally sophisticated therapeutics—including macrocyclic lactones, polyketides, terpenoids, alkaloids, and pharmacologically privileged scaffolds—continue to drive innovation, enzyme-mediated strategies provide mechanistically exquisite, environmentally consonant solutions that increasingly transcend the capabilities of traditional chemical catalysis. This review articulates the unifying principles and activation paradigms through which oxidoreductases, hydrolases, and transferases orchestrate the streamlined construction of architecturally dense natural products. In particular, emphasis is placed on cascade logic, mechanistically integrated chemoenzymatic platforms, and advances in enzyme engineering, which collectively furnish transformative blueprints for accessing next-generation bioactive architectures. By foregrounding conceptual frameworks rather than enumerating examples, this review positions biocatalysis as a central strategic axis at the intersection of synthetic methodology, chemical biology, and therapeutic discovery and as a driving force in shaping the future landscape of complex molecule synthesis (covering 2000–2025).

Abstract Image

Abstract Image

通过生物催化增强分子复杂性:医学相关天然产物全合成的新兴蓝图。
生物催化已经上升为当代全合成的决定性力量,提供了催化模式,以无与伦比的化学,区域和立体控制提供分子复杂性。随着结构复杂的治疗方法——包括大环内酯、聚酮、萜类、生物碱和药理学上优越的支架——不断推动创新,酶介导的策略提供了机制精致、环境协调的解决方案,日益超越传统化学催化的能力。这篇综述阐明了氧化还原酶、水解酶和转移酶的统一原理和激活模式,通过这些原理和模式,氧化还原酶、水解酶和转移酶协调了结构致密的天然产物的流线型结构。重点放在级联逻辑、机械集成的化学酶平台和酶工程的进展上,它们共同为获得下一代生物活性结构提供了变革性蓝图。通过强调概念框架而不是列举例子,本综述将生物催化定位为合成方法、化学生物学和治疗发现交叉点的中心战略轴,并将其作为塑造未来复杂分子合成景观的驱动力(涵盖2000-2025年)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
MedChemComm
MedChemComm BIOCHEMISTRY & MOLECULAR BIOLOGY-CHEMISTRY, MEDICINAL
CiteScore
4.70
自引率
0.00%
发文量
0
审稿时长
2.2 months
期刊介绍: Research and review articles in medicinal chemistry and related drug discovery science; the official journal of the European Federation for Medicinal Chemistry. In 2020, MedChemComm will change its name to RSC Medicinal Chemistry. Issue 12, 2019 will be the last issue as MedChemComm.
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