<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, 04 May 2026 13:31:36 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/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><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP90014C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP90014C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP90014C</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=D6NP90014C" /&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;,585-589&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D6NP90014C, 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 spectaterpenoid A from &lt;em&gt;Aspergillus spectabilis&lt;/em&gt;.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-04-16T00:00:00+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/D5NP00062A"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00062A</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00062A</link><title>Microbial natural products activated by plant stress</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=D5NP00062A" /&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;,590-596&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00062A, 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;Barbara I. Adaikpoh&lt;br/&gt;Highlighting studies that link plant stress to the activation of antimicrobial biosynthetic gene clusters in beneficial microbes, thereby illustrating chemical interactions in the plant's microenvironment that can inform natural product discovery.&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/">Barbara I. Adaikpoh</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00051C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00051C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00051C</link><title>Structure, bioactivity, biosynthesis, and synthesis of corynanthe 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=D5NP00051C" /&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;,746-778&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00051C, 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;Chenxu Liu, Mengqi Tong, Kouharu Otsuki, Wei Li, Feng Feng, Jie Zhang&lt;br/&gt;This paper reviews the structure, biosynthesis, synthesis, and activity of corynanthe alkaloids with the aim of providing new perspectives and discoveries for researchers in this field.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-01-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Chenxu Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mengqi Tong</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kouharu Otsuki</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wei Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Feng Feng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jie Zhang</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00061K"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00061K</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00061K</link><title>Microbe-derived aromatic polyketides toward MRSA infection: current advances and 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=D5NP00061K" /&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;,718-745&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00061K, Review Article&lt;/div&gt;&lt;div&gt;Fangfang Duan, Jiaying Lai, Linjie Wei, Siran Li, Polina Lopukhina, Zihuan Sang, Chen Chen, Xiaoyi Wei, Hongxin Liu, Haibo Tan&lt;br/&gt;Methicillin-resistant &lt;em&gt;Staphylococcus aureus&lt;/em&gt; (MRSA), one of the most common multidrug-resistant (MDR) bacterial strains, has severely threatened global healthcare for decades due to its high morbidity and mortality rates.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-01-23T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Fangfang Duan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiaying Lai</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Linjie Wei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Siran Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Polina Lopukhina</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zihuan Sang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chen Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoyi Wei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hongxin Liu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Haibo Tan</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00074B"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00074B</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00074B</link><title>Natural products modulating interleukin-mediated pathways for anti-allergic and immunomodulatory effects</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=D5NP00074B" /&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;,685-717&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00074B, 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;Abdul Bari Shah, Young Jun Kim, Kyeong Seon Lee, Sang Hoon Han, Youngjoo Byun, Ki Yong Lee&lt;br/&gt;The increasing prevalence of allergic diseases and immunological disorders is a significant public health issue requiring the development of novel therapeutic approaches.&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/">Abdul Bari Shah</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Young Jun Kim</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kyeong Seon Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sang Hoon Han</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Youngjoo Byun</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ki Yong Lee</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00046G"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00046G</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00046G</link><title>Discovery, bioactivities and biosynthesis of spirooxindole 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=D5NP00046G" /&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;,650-684&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00046G, 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;Ruijie Chen, Lihan Zhang, Xiaoyang Zhao, Zhuangjie Fang, Liping Zhang, Qingbo Zhang, Changsheng Zhang, Yiguang Zhu&lt;br/&gt;This review provides a comprehensive summary of the origin, activities, and biosynthesis of spirooxindole-containing alkaloids derived from a variety of organisms, including actinomycetes, cyanobacteria, fungi, plants, and invertebrates.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-01-05T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ruijie Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lihan Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoyang Zhao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhuangjie Fang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Liping Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Qingbo Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Changsheng Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yiguang Zhu</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00073D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00073D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00073D</link><title>Green gold of the Pacific: unlocking compounds from terrestrial flora for antitumor and immunomodulatory drug 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=D5NP00073D" /&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;,627-649&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00073D, 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;Paul Huchedé, Vincent Dumontet, Mariko Matsui&lt;br/&gt;This review highlights the Pacific region's terrestrial flora and explores its natural products as a source of novel antitumor and immunomodulatory compounds for drug discovery.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2026-01-05T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Paul Huchedé</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vincent Dumontet</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mariko Matsui</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00053J"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00053J</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00053J</link><title>A novel class of oligoarylamide antibiotics defined by albicidins and cystobactamids</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=D5NP00053J" /&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;,597-626&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/D5NP00053J, 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;Marcel Kulike-Koczula, Dominik Heimann, Tobias Eulberg, Daniel Kohnhäuser, Roderich D. Süssmuth, Mark Brönstrup&lt;br/&gt;This article summarizes insights on a new class of antibiotics defined by albicidins and cystobactamids. It presents their biosynthesis, total synthesis and lead optimization, the mechanisms of action and resistance, and the antibiotic properties.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;</description><a10:updated>2025-10-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Marcel Kulike-Koczula</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dominik Heimann</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tobias Eulberg</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Daniel Kohnhäuser</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Roderich D. Süssmuth</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Mark Brönstrup</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00081E"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00081E</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00081E</link><title>β-Lactam antibiotics and β-lactamases: historical perspectives and a review of β-lactamase inhibitors derived from 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=D5NP00081E" /&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/D5NP00081E, 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;Phanankosi Moyo, Ikhane O. Albert, Neo Hlungwani, Thulani Sibanda, Perfoy Lumu, Ndivhuwo Kevin Khorommbi, Gurleen Kaur, Karina Calvopina Tapia, George Siegwart, Nana Kwaku Buabeng, Cynthia A. Danquah, Lyndy J. McGaw, Sekelwa Cosa, Christopher J. Schofield, Vinesh J. Maharaj&lt;br/&gt;From the discovery of natural β-lactam antibiotics to the rise of serine and metallo-β-lactamases, this review traces their co-evolution and highlights microbial and plant-derived natural products as promising sources of new β-lactamase inhibitors.&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>2026-04-23T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Phanankosi Moyo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ikhane O. Albert</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Neo Hlungwani</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Thulani Sibanda</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Perfoy Lumu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ndivhuwo Kevin Khorommbi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gurleen Kaur</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Karina Calvopina Tapia</creator><creator xmlns="http://purl.org/dc/elements/1.1/">George Siegwart</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nana Kwaku Buabeng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cynthia A. Danquah</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lyndy J. McGaw</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sekelwa Cosa</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christopher J. Schofield</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vinesh J. Maharaj</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00090D"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00090D</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00090D</link><title>A comprehensive review of the structural diversity, biosynthesis and chemical synthesis of Lasiodiplodia spp. 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=D5NP00090D" /&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/D5NP00090D, 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;Maria Michela Salvatore, Marco Masi, Marina DellaGreca, Anna Andolfi&lt;br/&gt;&lt;em&gt;Lasiodiplodia&lt;/em&gt; is a prominent genus within the Botryosphaeriaceae family which is known as a plant pathogen. Species of &lt;em&gt;Lasiodiplodia&lt;/em&gt; are prolific sources of bioactive secondary metabolites.&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>2026-04-21T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Maria Michela Salvatore</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marco Masi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marina DellaGreca</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anna Andolfi</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00005C"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00005C</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D6NP00005C</link><title>Syntheses of furan 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=D6NP00005C" /&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/D6NP00005C, Review Article&lt;/div&gt;&lt;div&gt;Bichu Cheng&lt;br/&gt;This review discusses recent developments in the syntheses of furan natural products. The general methods for furan synthesis are extracted from total syntheses and categorized.&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>2026-04-20T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Bichu Cheng</creator></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00069F"><guid isPermaLink="true">http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00069F</guid><link>http://pubs.rsc.org/en/Content/ArticleLanding/2026/NP/D5NP00069F</link><title>New secondary metabolites isolated from Streptomyces species</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=D5NP00069F" /&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/D5NP00069F, Review Article&lt;/div&gt;&lt;div&gt;William J. Price Cunliffe, Peter J. Rutledge&lt;br/&gt;This review highlights novel secondary metabolites – including peptides, terpenoids, polyketides, alkaloids, and others – that were isolated from &lt;em&gt;Streptomyces&lt;/em&gt; bacteria and reported for the first time between 2021 and 2024.&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>2026-04-14T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">William J. Price Cunliffe</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peter J. Rutledge</creator></item><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></channel></rss>