{"title":"Unveiling Amaryllidaceae alkaloids: from biosynthesis to antiviral potential – a review","authors":"Thilina U. Jayawardena , Natacha Merindol , Nuwan Sameera Liyanage , Isabel Desgagné-Penix","doi":"10.1039/d3np00044c","DOIUrl":null,"url":null,"abstract":"<div><p>Covering: 2017 to 2023 (now)</p></div><div><p>Amaryllidaceae alkaloids (AAs) are a unique class of specialized metabolites containing heterocyclic nitrogen bridging that play a distinct role in higher plants. Irrespective of their diverse structures, most AAs are biosynthesized <em>via</em> intramolecular oxidative coupling. The complex organization of biosynthetic pathways is constantly enlightened by new insights owing to the advancement of natural product chemistry, synthetic organic chemistry, biochemistry, systems and synthetic biology tools and applications. These promote novel compound identification, trace-level metabolite quantification, synthesis, and characterization of enzymes engaged in AA catalysis, enabling the recognition of biosynthetic pathways. A complete understanding of the pathway benefits biotechnological applications in the long run. This review emphasizes the structural diversity of the AA specialized metabolites involved in biogenesis although the process is not entirely defined yet. Moreover, this work underscores the pivotal role of synthetic and enantioselective studies in justifying biosynthetic conclusions. Their prospective candidacy as lead constituents for antiviral drug discovery has also been established. However, a complete understanding of the pathway requires further interdisciplinary efforts in which antiviral studies address the structure–activity relationship. This review presents current knowledge on the topic.</p></div>","PeriodicalId":10,"journal":{"name":"ACS Central Science","volume":null,"pages":null},"PeriodicalIF":12.7000,"publicationDate":"2024-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Central Science","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S0265056824000278","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Covering: 2017 to 2023 (now)
Amaryllidaceae alkaloids (AAs) are a unique class of specialized metabolites containing heterocyclic nitrogen bridging that play a distinct role in higher plants. Irrespective of their diverse structures, most AAs are biosynthesized via intramolecular oxidative coupling. The complex organization of biosynthetic pathways is constantly enlightened by new insights owing to the advancement of natural product chemistry, synthetic organic chemistry, biochemistry, systems and synthetic biology tools and applications. These promote novel compound identification, trace-level metabolite quantification, synthesis, and characterization of enzymes engaged in AA catalysis, enabling the recognition of biosynthetic pathways. A complete understanding of the pathway benefits biotechnological applications in the long run. This review emphasizes the structural diversity of the AA specialized metabolites involved in biogenesis although the process is not entirely defined yet. Moreover, this work underscores the pivotal role of synthetic and enantioselective studies in justifying biosynthetic conclusions. Their prospective candidacy as lead constituents for antiviral drug discovery has also been established. However, a complete understanding of the pathway requires further interdisciplinary efforts in which antiviral studies address the structure–activity relationship. This review presents current knowledge on the topic.
覆盖时间:2017年至2023年(现在)金丝桃科生物碱(AAs)是一类独特的含有杂环氮桥的特殊代谢物,在高等植物中发挥着独特的作用。无论其结构如何变化,大多数 AAs 都是通过分子内氧化偶联进行生物合成的。随着天然产物化学、合成有机化学、生物化学、系统和合成生物学工具及应用的发展,人们对生物合成途径的复杂组织结构不断有新的认识。这些工具和应用促进了新型化合物的鉴定、痕量级代谢物的定量、合成以及参与 AA 催化的酶的表征,从而使生物合成途径得以识别。从长远来看,对途径的全面了解有利于生物技术的应用。本综述强调了参与生物合成的 AA 专化代谢物的结构多样性,尽管这一过程尚未完全明确。此外,这项工作还强调了合成和对映体选择性研究在证明生物合成结论方面的关键作用。它们作为抗病毒药物发现的先导成分的潜在候选资格也已确立。然而,要全面了解这一途径,还需要进一步的跨学科努力,在抗病毒研究中解决结构与活性的关系问题。本综述介绍了目前有关这一主题的知识。
期刊介绍:
ACS Central Science publishes significant primary reports on research in chemistry and allied fields where chemical approaches are pivotal. As the first fully open-access journal by the American Chemical Society, it covers compelling and important contributions to the broad chemistry and scientific community. "Central science," a term popularized nearly 40 years ago, emphasizes chemistry's central role in connecting physical and life sciences, and fundamental sciences with applied disciplines like medicine and engineering. The journal focuses on exceptional quality articles, addressing advances in fundamental chemistry and interdisciplinary research.