<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, 29 Jun 2026 17:28:18 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/D6NP00038J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00038J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00038J</link><title>Visual cycle-derived bisretinoids as endogenous natural products: enzyme-free formation, photochemical reactivity, and retinal degeneration</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=D6NP00038J" /&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/D6NP00038J, 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;Hye Jin Kim, Janet R. Sparrow, Young Pyo Jang&lt;br/&gt;This review reframes retinal bisretinoids as autochthonous natural products, demonstrating how polyene electrophilicity and non-enzymatic aza-electrocyclization dictate their inevitable biogenesis and subsequent photochemical toxicity.&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>2026-06-29T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hye Jin Kim</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Janet R. Sparrow</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Young Pyo Jang</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00077G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00077G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00077G</link><title>Non-strigolactone natural products interfering with parasitic weed development</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=D5NP00077G" /&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/D5NP00077G, 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;Jesús G. Zorrilla, Antonio Cala Peralta, Mónica Fernández-Aparicio, Marco Masi, Francisco A. Macías, Alessio Cimmino&lt;br/&gt;Non-strigolactone compounds regulate parasitic plant germination, growth, and host recognition, often acting synergistically with root signals. They also affect chemotropism and haustorium formation, revealing a complex chemical network.&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>2026-06-29T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jesús G. Zorrilla</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Antonio Cala Peralta</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mónica Fernández-Aparicio</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marco Masi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Francisco A. Macías</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alessio Cimmino</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00048G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00048G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00048G</link><title>Biosynthetic crosstalk in bacteria: routes to chimeric 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=D6NP00048G" /&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/D6NP00048G, 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-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;Wen-Chao Yu, Zhiyuan Peng, Yan-Song Ye, Qihao Wu&lt;br/&gt;Distributed biosynthetic pathways can generate chimeric natural products missed by single cluster genome mining; multi-class metabolomics offers a route to identify these overlooked hybrid scaffolds.&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>2026-06-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wen-Chao Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhiyuan Peng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yan-Song Ye</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qihao Wu</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00052E"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00052E</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00052E</link><title>Genomic scale analysis of assembly-line polyketide synthase diversity and evolution</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=D6NP00052E" /&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/D6NP00052E, Review Article&lt;/div&gt;&lt;div&gt;Seokyoung Lee, Chaitan Khosla&lt;br/&gt;PKSClusterDB provides a curated genomic-scale catalogue of assembly-line PKSs, enabling anchor-window analysis that reveals family-resolved evolutionary patterns and helps interpret orphan pathways and biosynthetic 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>2026-06-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Seokyoung Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chaitan Khosla</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00015K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00015K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00015K</link><title>Asymmetric synthesis of 3,3-disubstituted oxindoles: methodologies and applications 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=D6NP00015K" /&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/D6NP00015K, Review Article&lt;/div&gt;&lt;div&gt;Rui Yang, Lihua Wei, Zhiqiang Ma&lt;br/&gt;This review summarizes the diverse asymmetric strategies for constructing 3,3-disubstituted oxindoles and discusses their applications in natural product synthesis, with an emphasis on the construction of the key chiral intermediates.&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>2026-06-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Rui Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lihua Wei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhiqiang Ma</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP90018F"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP90018F</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP90018F</link><title>Mass spectrometry as the unifying force in natural product sciences</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=D6NP90018F" /&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;,1070-1072&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6NP90018F, Editorial&lt;/div&gt;&lt;div&gt;Mehdi A. Beniddir, Nadja B. Cech, Roger Linington, Neha Garg&lt;br/&gt;Mehdi A. Beniddir, Nadja B. Cech, Roger Linington and Neha Garg introduce the &lt;em&gt;Natural Product Reports&lt;/em&gt; themed issue on Mass spectrometry metabolomics in natural products research.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-06-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Mehdi A. Beniddir</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nadja B. Cech</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Roger Linington</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Neha Garg</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP90022D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP90022D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP90022D</link><title>Hot off the Press</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=D6NP90022D" /&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;,1073-1077&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6NP90022D, Hot off the Press Article&lt;/div&gt;&lt;div&gt;Robert A. Hill, Andrew Sutherland&lt;br/&gt;A personal selection of 32 recent papers is presented covering various aspects of current developments in bioorganic chemistry and novel natural products such as humupulusone A from &lt;em&gt;Humulus lupulus&lt;/em&gt;.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-06-10T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Robert A. Hill</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrew Sutherland</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00040H"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00040H</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00040H</link><title>Cultivar to chemotype: characterizing complex botanicals with mass spectrometry metabolomics</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=D5NP00040H" /&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;,1181-1200&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00040H, 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;Joshua J. Kellogg, R. Teal Jordan, Madhusha M. Ranaweera, Kelsey Custer, Savannah G. Anez, Julia Bendlin, Francisco T. Chacon, Xiaoling Chen&lt;br/&gt;To ensure safe and effective botanical products, the identity and integrity of the source material is essential. Mass spectrometry-based metabolomics provides a powerful, sensitive analytical tool to characterize these complicated chemical mixtures.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2025-12-03T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Joshua J. Kellogg</creator><creator xmlns="http://purl.org/dc/elements/1.1/">R. Teal Jordan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Madhusha M. Ranaweera</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kelsey Custer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Savannah G. Anez</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Julia Bendlin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Francisco T. Chacon</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoling Chen</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00022J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00022J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00022J</link><title>Metabolism and bioavailability aspects of natural products of plant origin using mass spectrometry-based and metabolomic approaches</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=D5NP00022J" /&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;,1130-1180&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00022J, 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;Eleni V. Mikropoulou, Aikaterini Basdeki, Maria Halabalaki&lt;br/&gt;This review investigates the journey of metabolite identification and quantification of natural products (NPs), exploiting mass spectrometry approaches from the early 1980s to the current developments in this field.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2025-10-28T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Eleni V. Mikropoulou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Aikaterini Basdeki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Maria Halabalaki</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00034C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00034C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00034C</link><title>Scalability of mass spectrometry-based metabolomics for natural extracts libraries exploration: current status, challenges, and opportunities</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=D5NP00034C" /&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;,1106-1129&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00034C, 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;Adriano Rutz, Wout Bittremieux, Robin Schmid, Olivier Cailloux, Justin J. J. van der Hooft, Mehdi A. Beniddir&lt;br/&gt;This review aims at highlighting how scalability of the mass spectrometry-based discovery pipeline plays a pivotal role in finding novel bioactives in natural extracts libraries.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2025-09-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Adriano Rutz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wout Bittremieux</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Robin Schmid</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Olivier Cailloux</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Justin J. J. van der Hooft</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mehdi A. Beniddir</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00021A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00021A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00021A</link><title>Mass spectrometry-based metabolomics approaches to interrogate host–microbiome interactions in mammalian systems</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=D5NP00021A" /&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;,1078-1105&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00021A, 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;Atharva S. Kulkarni, Guilherme M. P. Carrara, Jiangpeiyun Jin, Jarrod Laro, Thilini Peramuna, Laura-Isobel McCall, Neha Garg&lt;br/&gt;Chemical crosstalk is universal to all life, niche-specific, and essential to thrive.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2025-06-16T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Atharva S. Kulkarni</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guilherme M. P. Carrara</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiangpeiyun Jin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jarrod Laro</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Thilini Peramuna</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Laura-Isobel McCall</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Neha Garg</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00030D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00030D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00030D</link><title>The elansolids: how nature shows chemists how to tame p-quinone methides</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=D6NP00030D" /&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/D6NP00030D, 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;Liang-Liang Wang, Xiao-Qin Zhou, Andreas Kirschning&lt;br/&gt;Using elansolids as a case study, it is demonstrated how nature tames the highly reactive &lt;em&gt;p&lt;/em&gt;-quinone methide by controlling its reactivity and conformation in a very efficient manner.&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>2026-06-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Liang-Liang Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiao-Qin Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andreas Kirschning</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00008H"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00008H</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00008H</link><title>Challenges and opportunities in the synthesis of biologically relevant flavonoids and their glycosides</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=D6NP00008H" /&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/D6NP00008H, 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;Debabrata Giri, Saikat Mondal, M. Carmen Galan, Abhijit Sau&lt;br/&gt;This review provides a current perspective on the recent advancements in flavonoid chemistry and their role in the development of novel therapeutic agents.&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>2026-06-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Debabrata Giri</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Saikat Mondal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">M. Carmen Galan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Abhijit Sau</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00084J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00084J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00084J</link><title>Cinnamoyl-containing non-ribosomal peptides: discovery, bioactivity and 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=D5NP00084J" /&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/D5NP00084J, Review Article&lt;/div&gt;&lt;div&gt;Yuyang Wang, Yanqing Li, Yingying Chen, Jianhua Ju, Zhuo Shang, Junying Ma&lt;br/&gt;The chemical diversity, biological activities, biosynthesis and expanding chemical diversity of cinnamoyl-containing non-ribosomal peptides.&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>2026-06-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yuyang Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yanqing Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yingying Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jianhua Ju</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhuo Shang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Junying Ma</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00022C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00022C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00022C</link><title>Decoding multidimensional regulatory networks in Streptomyces to accelerate natural product discovery and production</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=D6NP00022C" /&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/D6NP00022C, Review Article&lt;/div&gt;&lt;div&gt;Yongjae Lee, Woori Kim, Chanyoung Joung, Hyeseong Kim, Namil Lee, Byung-Kwan Cho&lt;br/&gt;Advances in genome-scale analytical tools have expanded our knowledge of regulatory networks in &lt;em&gt;Streptomyces&lt;/em&gt;, providing a transferable framework for the systematic activation of biosynthetic gene clusters for natural product discovery and 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>2026-06-18T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yongjae Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Woori Kim</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chanyoung Joung</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hyeseong Kim</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Namil Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Byung-Kwan Cho</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00018E"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00018E</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00018E</link><title>Ecological context for bacterial natural products 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=D6NP00018E" /&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/D6NP00018E, 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;Jonathan Parra, Marla I. Macias-Contreras, Dulce G. Guillén Matus, Katherine R. Duncan&lt;br/&gt;This review highlights recent studies and considerations towards ecological approaches to natural product discovery.&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>2026-06-11T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jonathan Parra</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marla I. Macias-Contreras</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dulce G. Guillén Matus</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Katherine R. Duncan</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00011H"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00011H</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00011H</link><title>Emerging technologies for the discovery of biosynthetic genes in plants</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=D6NP00011H" /&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/D6NP00011H, 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;Anne Jaczkowski, Arne Bültemeier, Benedikt Seligmann, Boas Pucker, Jakob Franke&lt;br/&gt;Compared to microbial natural product research, elucidating biosynthetic pathways in plants requires distinct methodological approaches. This review describes emerging technologies for discovering biosynthetic genes in plants.&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>2026-06-11T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Anne Jaczkowski</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Arne Bültemeier</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Benedikt Seligmann</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Boas Pucker</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jakob Franke</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00039H"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00039H</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00039H</link><title>Microbial biotransformation of plant-derived metabolites: mechanisms, pathways, and multi-omics integration</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=D6NP00039H" /&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/D6NP00039H, Review Article&lt;/div&gt;&lt;div&gt;Youngse Oh, Jaeyoun Lee, Soohyun Um, Seung Hyun Kim&lt;br/&gt;This review presents a reaction-class atlas of microbial biotransformations of plant-derived metabolites and highlights how enzymatic mechanisms and multi-omics approaches reveal metabolic diversity in complex microbial communities.&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>2026-06-10T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Youngse Oh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jaeyoun Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Soohyun Um</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Seung Hyun Kim</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00012F"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00012F</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00012F</link><title>Rare functional groups and unique scaffolds in Streptomyces 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=D6NP00012F" /&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/D6NP00012F, Review Article&lt;/div&gt;&lt;div&gt;Sanyuan Shi, Xuerui Jin, Gaoli Wang, Xuewei Hao, Jing Xie, Liujie Huo, Yunzi Luo&lt;br/&gt;This review highlights &lt;em&gt;Streptomyces&lt;/em&gt; natural products with rare functional groups, unique scaffolds, and atypical modifications, examining the enzymatic mechanisms to link biosynthetic diversity with synthetic biology applications.&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>2026-06-08T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sanyuan Shi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xuerui Jin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gaoli Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xuewei Hao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jing Xie</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Liujie Huo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yunzi Luo</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00003G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00003G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00003G</link><title>Advances in the discovery and functional analysis of Anti-infective and immunomodulatory natural products from host-associated microbiomes</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=D6NP00003G" /&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/D6NP00003G, 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;Sebastian Götze, Christine Beemelmanns&lt;br/&gt;This review highlights discoveries from 2018 to 2025 of microbiome-derived natural products with anti-infective and immunomodulatory actvities, and urges to more targeted OMICs approaches to fully harness the encoded biosynthetic capacity.&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>2026-06-05T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sebastian Götze</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christine Beemelmanns</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00083A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00083A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00083A</link><title>Natural products with atypical atoms: unveiling structures, biosynthetic pathways, and bioactivities</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=D5NP00083A" /&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/D5NP00083A, 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;Yeo Jin Lee, Hyeon-Jeong Hwang, Jungro Lee, Hyeon Seung Park, Juwan Son, Mohammad Seyedsayamdost, Munhyung Bae, Seoung Rak Lee, Yun Kwon&lt;br/&gt;Rare elements in natural products unlock new chemical space, biosynthetic logic, and biological activities.&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>2026-06-04T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yeo Jin Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hyeon-Jeong Hwang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jungro Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hyeon Seung Park</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Juwan Son</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mohammad Seyedsayamdost</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Munhyung Bae</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Seoung Rak Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yun Kwon</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00014B"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00014B</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00014B</link><title>Inverse stable isotopic labeling for natural product characterization and 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=D6NP00014B" /&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/D6NP00014B, 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;Jose Miguel D. Robes, Aaron W. Puri&lt;br/&gt;This review highlights applications of inverse stable isotope labeling in natural product research, including biosynthesis, structural elucidation, and discovery, spanning 2005 to 2026.&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>2026-06-03T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jose Miguel D. Robes</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Aaron W. Puri</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00034G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00034G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00034G</link><title>Unlocking hidden enzymatic chemistry in 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=D6NP00034G" /&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/D6NP00034G, Highlight&lt;/div&gt;&lt;div&gt;Micah Harris, Asher Paul, Edward Kalkreuter&lt;br/&gt;This highlight reviews many of the existing and emerging strategies for prioritizing and accessing novel enzymology from microbial 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>2026-06-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Micah Harris</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Asher Paul</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Edward Kalkreuter</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00027D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00027D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00027D</link><title>Synthetic biology as a game-changer for endangered medicinal orchids: biosynthesis, engineering and conservation</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=D6NP00027D" /&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/D6NP00027D, Review Article&lt;/div&gt;&lt;div&gt;Lin Qiu, Xianghui Chen, Zhan Luo, Min Jiang, Hu Chen, Biyu Hou, Haizheng Yu, Ning Li, Lei Zhang&lt;br/&gt;Synthetic biology acts as a game-changer for endangered medicinal orchids, enabling a transition from resource scarcity and extraction inefficiency to sustainable conservation through pathway decoding, chassis engineering and green biomanufacturing.&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>2026-06-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Lin Qiu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xianghui Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhan Luo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Min Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hu Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Biyu Hou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Haizheng Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ning Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lei Zhang</creator></item></channel></rss>