<rss version="2.0" xmlns:a10="http://www.w3.org/2005/Atom"><channel><title>RSC - Nat. Prod. Rep. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/NP</link><description>RSC - Nat. Prod. Rep. latest articles</description><copyright>Copyright (c)  The Royal Society of Chemistry</copyright><lastBuildDate>Fri, 29 May 2026 21:31:30 Z</lastBuildDate><category>RSC - Nat. Prod. Rep. latest articles</category><image><url>http://pubs.rsc.org/content/NewImages/rsc_publishing_logo.gif</url><title>RSC - Nat. Prod. Rep. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/NP</link></image><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00091B"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00091B</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00091B</link><title>Charting the path for L-tyrosine derivatives: from engineering strategies to microbial cell factories</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5NP00091B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;43&lt;/b&gt;,1026-1062&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00091B, Review Article&lt;/div&gt;&lt;div&gt;Li Zhou, Xulei Shi, Hui Jiang, Yuanyuan Xia, Haiquan Yang, Wei Shen, Yu Cao, Xianzhong Chen&lt;br/&gt;Review highlights cutting-edge advances in producing &lt;small&gt;L&lt;/small&gt;-tyrosine derivatives &lt;em&gt;via&lt;/em&gt; tyrosol, &lt;em&gt;p&lt;/em&gt;-coumaric acid, and &lt;small&gt;L&lt;/small&gt;-DOPA nodes in &lt;em&gt;E. coli&lt;/em&gt; and yeast.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-24T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Li Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xulei Shi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hui Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuanyuan Xia</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Haiquan Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wei Shen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yu Cao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xianzhong Chen</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00076A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00076A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00076A</link><title>Highlights of cyanobacterial metabolites reported between 2021–2024</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5NP00076A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;43&lt;/b&gt;,1008-1025&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00076A, Review Article&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Simon Sieber, Elisabeth M.-L. Janssen&lt;br/&gt;This review provides an overview of newly identified cyanobacterial metabolites from 2021 to 2024. The discovery of specific natural products is discussed.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-16T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Simon Sieber</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Elisabeth M.-L. Janssen</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00010J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00010J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00010J</link><title>Decision making by modular polyketide synthases and implications for genetic engineering</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6NP00010J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;43&lt;/b&gt;,961-1007&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6NP00010J, Review Article&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY-NC.png' alt='Creative Commons Licence' border='none'/&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution-NonCommercial 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Kira J. Weissman&lt;br/&gt;This review details the many choices underlying faithful biosynthesis of complex polyketides in bacteria, and highlights the implications for genetic engineering aiming to generate novel derivatives.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kira J. Weissman</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00087D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00087D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00087D</link><title>Quinic acid as a chiron in total synthesis</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5NP00087D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;43&lt;/b&gt;,932-960&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00087D, Review Article&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Manuel J. Verganista, Iago C. Vogel, Nuno R. Candeias&lt;br/&gt;Quinic acid is a versatile chiral building block in asymmetric synthesis, enabling diverse natural products and bioactive compounds. This review highlights four decades of strategies, applications and new trends in complex molecule construction.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-03T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Manuel J. Verganista</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Iago C. Vogel</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nuno R. Candeias</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00068H"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00068H</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00068H</link><title>Microbial production of C7–C9 aromatic building blocks for the production of natural products</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5NP00068H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;43&lt;/b&gt;,897-931&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00068H, Review Article&lt;/div&gt;&lt;div&gt;Qiaoqiao Dai, Jiaqi Xu, Jing Wu, Xiaomin Li, Cong Gao, Guipeng Hu, Liming Liu&lt;br/&gt;This review surveys representative C&lt;small&gt;&lt;sub&gt;7&lt;/sub&gt;&lt;/small&gt;–C&lt;small&gt;&lt;sub&gt;9&lt;/sub&gt;&lt;/small&gt; aromatic compounds, outlining their microbial biosynthetic pathways, key metabolic challenges, and recent advances in metabolic engineering for their microbial production.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-02-23T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Qiaoqiao Dai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiaqi Xu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jing Wu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaomin Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cong Gao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guipeng Hu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Liming Liu</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00085H"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00085H</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00085H</link><title>Isolation and synthesis of bisabosquals, fungal triprenyl phenol meroterpenoids with a densely functionalised bisabolane core</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5NP00085H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;43&lt;/b&gt;,803-812&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00085H, Highlight&lt;/div&gt;&lt;div&gt;James P. Shephard, David W. Lupton&lt;br/&gt;Bisabosquals and &lt;em&gt;seco&lt;/em&gt;-bisabosquals are unusual fungal meroterpenoids with a densely functionalised bisabolane core. Herein, we highlight their isolation, biosynthesis and bioactivities along with studies on their total syntheses.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-02-02T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">James P. Shephard</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David W. Lupton</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00067J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00067J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00067J</link><title>Natural product inspired antibiotics approved for human use – 1943 to 2025</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5NP00067J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;43&lt;/b&gt;,813-896&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00067J, Review Article&lt;/div&gt;&lt;div&gt;Mark S. Butler, Robert J. Capon&lt;br/&gt;This review captures the legacy of natural products in shaping modern infection control and highlights their potential for delivering the next generation of life-saving antibiotics.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2025-12-11T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mark S. Butler</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Robert J. Capon</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00059A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00059A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00059A</link><title>AI and mechanistic modeling for characterizing biosynthetic pathways of natural products</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5NP00059A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2026, &lt;b&gt;43&lt;/b&gt;,787-802&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00059A, Highlight&lt;/div&gt;&lt;div&gt;Byung Tae Lee, Byeongsub Lee, Joon Young Kwon, Tilmann Weber, Hyun Uk Kim&lt;br/&gt;Integrating AI-driven and mechanistic modeling accelerates the discovery and engineering of natural product biosynthetic pathways.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2025-11-07T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Byung Tae Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Byeongsub Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Joon Young Kwon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tilmann Weber</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hyun Uk Kim</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00013D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00013D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00013D</link><title>From gene discovery to synthetic biology: recent advances in the biosynthesis of oleanane-type pentacyclic triterpenoids</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6NP00013D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6NP00013D, Review Article&lt;/div&gt;&lt;div&gt;Ismail Abdelsamad, Mohamed Abdulbagi, Jingya Wang, Zheyong Xue, Xu Lu&lt;br/&gt;This review discusses recent progress in biosynthetic enzymes, regulatory networks, and synthetic biology strategies for oleanane-type triterpenoids, including AI-driven predictive optimization for sustainable production.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ismail Abdelsamad</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mohamed Abdulbagi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jingya Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zheyong Xue</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xu Lu</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00002A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00002A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00002A</link><title>Chemical language models for natural product discovery</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6NP00002A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6NP00002A, Review Article&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Koh Sakano, Kairi Furui, Apakorn Kengkanna, Yuta Kikuchi, Masahito Ohue&lt;br/&gt;Natural products are an important source of medicines, yet their discovery can be a slow and laborious process.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-12T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Koh Sakano</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kairi Furui</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Apakorn Kengkanna</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuta Kikuchi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Masahito Ohue</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00089K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00089K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00089K</link><title>Recent advances in decoding biosynthetic pathways and synthetic biology approaches for plant alkaloids</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5NP00089K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00089K, Review Article&lt;/div&gt;&lt;div&gt;Lanyu Zhou, Haiyue Gong, Huan Zhao, Luqi Huang, Yating Hu&lt;br/&gt;This review analyzes advances in plant alkaloid biosynthesis (2018–2025), highlighting key challenges in stereochemical control, cyclization, and tailoring modifications, and discusses synthetic biology strategies for microbial production.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-12T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Lanyu Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Haiyue Gong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huan Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Luqi Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yating Hu</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00016A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00016A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00016A</link><title>Structural determination of natural products at speeds and scale of high-throughput screening</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6NP00016A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6NP00016A, Review Article&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY-NC.png' alt='Creative Commons Licence' border='none'/&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by-nc/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution-NonCommercial 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Christopher C. Thornburg, Rohitesh Kumar, Dongdong Wang, Barry R. O'Keefe, Tanja Grkovic&lt;br/&gt;This review highlights analytical techniques and methods used for the structural elucidation of natural products in high-throughput screening campaigns.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-11T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Christopher C. Thornburg</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rohitesh Kumar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dongdong Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Barry R. O'Keefe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tanja Grkovic</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00006A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00006A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00006A</link><title>High-throughput assays for SAM-dependent methyltransferases: advances, challenges, and future perspectives</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6NP00006A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6NP00006A, Review Article&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Renia Fotiadou, Florian Heinz, Konstantin F. G. Weigmann, Mark Doerr, Uwe T. Bornscheuer, Ioannis V. Pavlidis&lt;br/&gt;High-throughput assays for SAM-dependent methyltransferases are useful tools for protein engineering efforts and beyond; advances, limitations, and future opportunities are herein critically reviewed.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-05T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Renia Fotiadou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Florian Heinz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Konstantin F. G. Weigmann</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mark Doerr</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Uwe T. Bornscheuer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ioannis V. Pavlidis</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00004E"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00004E</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00004E</link><title>Skeleton innovation versus structural diversification in terpenoid discovery: chemoinformatic insights from TeroKit</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D6NP00004E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6NP00004E, Highlight&lt;/div&gt;&lt;div&gt;Tao Zeng, Jiahao Li, Ruibo Wu&lt;br/&gt;Contrasting skeletal exploration with structural exploitation reveals a clear reality: terpenoid discovery in the past six years is overwhelmingly dominated by the modification-driven exploitation of established skeletons.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Tao Zeng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiahao Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ruibo Wu</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00072F"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00072F</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00072F</link><title>Advancing natural product R&amp;D&amp;I: guide for compliance with responsible research and innovation, ethics, Nagoya and Cartagena Protocols, and intellectual property protection</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=D5NP00072F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2026, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00072F, Review Article&lt;/div&gt;&lt;div&gt;&lt;img  alt='Open Access' src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/open_access_blue.png' /&gt; Open Access&lt;/div&gt;&lt;div&gt;&lt;a rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window'&gt; &lt;img src='http://sod-a.rsc-cdn.org/pubs.rsc-uat.org/content/NewImages/CCBY.png' alt='Creative Commons Licence' border='none' /&gt;&lt;/a&gt;&amp;nbsp This article is licensed under a &lt;a text-decoration=none rel='license' href='http://creativecommons.org/licenses/by/3.0/' target='_blank' title='This link will open in a new browser window' &gt;Creative Commons Attribution 3.0 Unported Licence.&lt;/a&gt;&lt;/div&gt;&lt;div&gt;Susana P. Gaudêncio, Belma Kalamujić Stroil, Lucie Novoveska, Céline Rebours, Xenia T. Schneider&lt;br/&gt;RRI, ethical standards, the Nagoya and Cartagena Protocols, and IP frameworks influence natural products R&amp;amp;D&amp;amp;I and the bioeconomy, providing a foundation for sustainable and equitable resource use while promoting innovation and growth.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Susana P. Gaudêncio</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Belma Kalamujić Stroil</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lucie Novoveska</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Céline Rebours</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xenia T. Schneider</creator></item></channel></rss>