<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>Mon, 13 Apr 2026 14:45:59 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/D6NP00024J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00024J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00024J</link><title>Construction of C(sp3)–C(sp3) attached ring motifs in natural product 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=D6NP00024J" /&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/D6NP00024J, Review Article&lt;/div&gt;&lt;div&gt;Søren L. B. Møller, Thomas B. Poulsen&lt;br/&gt;A survey of synthetic approaches to saturated C(sp³)–C(sp³) attached ring systems in natural products, with emphasis on direct fragment couplings that enable efficient assembly of complex polycyclic frameworks.&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>2026-04-10T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Søren L. B. Møller</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Thomas B. Poulsen</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00092K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00092K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00092K</link><title>Fungal polyketide biosynthesis as a platform for designer 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=D5NP00092K" /&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/D5NP00092K, 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;Pingxin Lin, Zhenhao Fu, Ye Li, Yeo Joon Yoon, Sang Yup Lee&lt;br/&gt;Programming rules of fungal iterative polyketide synthases enable combinatorial biosynthesis and cell-factory engineering to expand polyketide chemical diversity.&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>2026-04-07T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Pingxin Lin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhenhao Fu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ye Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yeo Joon Yoon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sang Yup Lee</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00007J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00007J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00007J</link><title>The isolation, biosynthesis, biological profiles and synthesis of the pterocarpans, pterocarpenes and coumestans: isoflavone derivatives with pharmacological utility</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=D6NP00007J" /&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/D6NP00007J, Review Article&lt;/div&gt;&lt;div&gt;Liangguang (Jack) Yi, Lorenzo V. White, Martin G. Banwell&lt;br/&gt;The title compounds are three structurally related classes of isoflavone that often act as phytoalexins in the producing plants. This review highlights their biological profiles that make them ongoing targets for synthesis and drug development.&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>2026-03-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Liangguang (Jack) Yi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lorenzo V. White</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Martin G. Banwell</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00020C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00020C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00020C</link><title>Synthetic biology for heterologous expression and engineering of fungal polyketide synthases</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=D5NP00020C" /&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;,401-414&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00020C, Highlight&lt;/div&gt;&lt;div&gt;Sidharth Jayachandran, Adrian Enrique Gadar-Lopez, Ling Chen, Kasper Krunderup Jakobsen, Coco Xie, Therese Horch, Jay D. Keasling, Pablo Cruz-Morales&lt;br/&gt;Polyketide synthases (PKSs) are essential enzymatic systems that produce a wide range of natural products.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-03-02T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sidharth Jayachandran</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Adrian Enrique Gadar-Lopez</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ling Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kasper Krunderup Jakobsen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Coco Xie</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Therese Horch</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jay D. Keasling</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pablo Cruz-Morales</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00065C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00065C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00065C</link><title>Trimeric natural products: structural diversity, biosynthesis, bioactivities and chemical 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=D5NP00065C" /&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;,462-496&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00065C, Review Article&lt;/div&gt;&lt;div&gt;Hidayat Hussain, Satyajit D. Sarker, Lutfun Nahar, Ishtiaq Ahmed&lt;br/&gt;This review highlights structural diversity, biosynthesis, biomimetic synthesis, and biological functions of trimeric natural products. These biosynthetic pathways could lead to the discovery of more bioactive trimers through (bio)synthesis.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-01-22T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hidayat Hussain</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Satyajit D. Sarker</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lutfun Nahar</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ishtiaq Ahmed</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00075K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00075K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00075K</link><title>Discovery, engineering, and applications of amino acid and peptide prenyltransferases</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=D5NP00075K" /&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;,415-426&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00075K, Highlight&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;Florian Hubrich&lt;br/&gt;This review highlights advances in the field of amino acid and peptide prenyltransferases, underscoring their value for chemoenzymatic peptide late-stage functionalization and drug development and showcasing their scope, promiscuity and engineering.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-01-02T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Florian Hubrich</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00056D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00056D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00056D</link><title>Biosynthesis of invertebrate-derived natural products: an uncharted territory</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=D5NP00056D" /&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;,547-575&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00056D, Review Article&lt;/div&gt;&lt;div&gt;Feng Li, Chengyu Zhou, Yinhao Wang, Mengmeng Yu, Jianhua Ju&lt;br/&gt;Invertebrates are a major source of natural products. Their significant biosynthetic potential, revealed by recent studies, is summarized in this review as a reference for future research.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2025-12-22T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Feng Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chengyu Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yinhao Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mengmeng Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianhua Ju</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00078E"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00078E</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00078E</link><title>Microbial skeletal editing: hints for arene reconstruction from actinobacteria</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=D5NP00078E" /&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;,518-546&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00078E, Review Article&lt;/div&gt;&lt;div&gt;Viktoria A. Ikonnikova, Vera A. Alferova, Anastasiya Yu. Frolova, Mikhail S. Baranov, Andrey A. Mikhaylov&lt;br/&gt;This review surveys skeletal editing in actinobacteria, linking enzyme-driven diversification to modern synthetic analogues and outlining biomimetic strategies that translate natural logic into practical chemical tools.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2025-12-22T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Viktoria A. Ikonnikova</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vera A. Alferova</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anastasiya Yu. Frolova</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mikhail S. Baranov</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrey A. Mikhaylov</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00058K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00058K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00058K</link><title>From diet to defence: ingestion, sequestration, biotransformation, and therapeutic potential of natural products in nudibranch predator–prey interactions</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=D5NP00058K" /&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;,497-517&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00058K, Review Article&lt;/div&gt;&lt;div&gt;Lauren Gris, Michèle R. Prinsep&lt;br/&gt;This review focuses on the chemoecological interactions reported between nudibranchs and their marine invertebrate prey, highlighting the ingestion, sequestration and biotransformation of diet-derived natural products and their bioactivities.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2025-12-17T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Lauren Gris</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michèle R. Prinsep</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00055F"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00055F</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00055F</link><title>Halogenases and dehalogenases: mechanisms, engineering, and applications</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=D5NP00055F" /&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;,427-461&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00055F, Review Article&lt;/div&gt;&lt;div&gt;Jing Luo, Na Li, Jia Wang, Yaojie Gao, Hongzhi Tang, Linquan Bai, Sang Yup Lee, Yaojun Tong&lt;br/&gt;Halogenases and dehalogenases are ubiquitous biocatalysts that mediate halogen incorporation and removal. Synthetic biology is reshaping their catalytic landscapes to unlock new functions and applications.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2025-11-03T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jing Luo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Na Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jia Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yaojie Gao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hongzhi Tang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Linquan Bai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sang Yup Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yaojun Tong</creator></item><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, Advance Article&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;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>2026-03-24T00:00:00Z</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/D5NP00071H"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00071H</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00071H</link><title>Glucose 6-phosphate: the diversity of C-methylation in sugar moieties within natural product biosynthesis</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=D5NP00071H" /&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/D5NP00071H, 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;Ziruo Zou, Michael Müller&lt;br/&gt;Diverse methylation of sugar units by SAM-dependent C-methyltransferases in natural product biosynthesis.&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>2026-03-16T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ziruo Zou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael Müller</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, Advance Article&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;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>2026-03-16T00:00:00Z</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></channel></rss>