<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wei J</submitter><funding>Shanxi Student's Innovation and Entrepreneurship Training Program</funding><funding>Scientific Research Start-up Foun-dation of Shangluo University</funding><funding>the Research and Innovation Team of Shangluo University</funding><funding>Key R&amp;D Projects in Shaanxi Province of China</funding><funding>Scientific Research Start-up Foundation of Shangluo University</funding><funding>Science and Technology Research Project of Shangluo University</funding><funding>PhD Research Start-up Fee of Shangluo University</funding><funding>Shanxi Student’s Innovation and Entrepreneurship Training Program</funding><funding>Key R&amp;amp;amp;D Projects in Shaanxi Province of China</funding><funding>Specialized Scientific Research Fund Projects of Academician Shengyong Zhang</funding><funding>Educational Commission of Shaanxi Province</funding><funding>Specialized Scientific Research Fund Projects</funding><pagination>6380</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10489798</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(17)</volume><pubmed_abstract>The culinary medicinal mushroom &lt;i>Hericium erinaceus&lt;/i> holds significant global esteem and has garnered heightened interest within increasingly ageing societies due to its pronounced neuroprotective and anti-neuroinflammatory properties. Within this study, two novel diterpenes, 16-carboxy-13-&lt;i>epi&lt;/i>-neoverrucosane (&lt;b>1&lt;/b>) and Erinacine L (&lt;b>2&lt;/b>); three known xylosyl cyathane diterpenoids, Erinacine A (&lt;b>3&lt;/b>), Erinacine C (&lt;b>4&lt;/b>), and Erinacine F (&lt;b>5&lt;/b>); and four lanostane-type triterpenoids, and three cyclic dipeptides (&lt;b>10&lt;/b>-&lt;b>12&lt;/b>), in addition to orcinol (&lt;b>13&lt;/b>), were isolated from the rice-based cultivation medium of &lt;i>H. erinaceus&lt;/i>. Their structures were determined by NMR, HR-ESI-MS, ECD, and calculated NMR. Compound &lt;b>1&lt;/b> marks a pioneering dis</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Unprecedented Neoverrucosane and Cyathane Diterpenoids with Anti-Neuroinflammatory Activity from Cultures of the Culinary-Medicinal Mushroom &lt;i>Hericium erinaceus&lt;/i>.</pubmed_title><pmcid>PMC10489798</pmcid><funding_grant_id>20JY009</funding_grant_id><funding_grant_id>18YSZX004</funding_grant_id><funding_grant_id>16SKY023, 22SKY106</funding_grant_id><funding_grant_id>2023-YBSF-164</funding_grant_id><funding_grant_id>16SKY023</funding_grant_id><funding_grant_id>19SCX05</funding_grant_id><funding_grant_id>22SKY106</funding_grant_id><funding_grant_id>S202211396060</funding_grant_id><funding_grant_id>20SKY010</funding_grant_id><pubmed_authors>Qi J</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Feng XL</pubmed_authors><pubmed_authors>Hu X</pubmed_authors><pubmed_authors>Hui H</pubmed_authors><pubmed_authors>Wei J</pubmed_authors><pubmed_authors>Li JY</pubmed_authors><pubmed_authors>Xue X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Unprecedented Neoverrucosane and Cyathane Diterpenoids with Anti-Neuroinflammatory Activity from Cultures of the Culinary-Medicinal Mushroom &lt;i>Hericium erinaceus&lt;/i>.</name><description>The culinary medicinal mushroom &lt;i>Hericium erinaceus&lt;/i> holds significant global esteem and has garnered heightened interest within increasingly ageing societies due to its pronounced neuroprotective and anti-neuroinflammatory properties. Within this study, two novel diterpenes, 16-carboxy-13-&lt;i>epi&lt;/i>-neoverrucosane (&lt;b>1&lt;/b>) and Erinacine L (&lt;b>2&lt;/b>); three known xylosyl cyathane diterpenoids, Erinacine A (&lt;b>3&lt;/b>), Erinacine C (&lt;b>4&lt;/b>), and Erinacine F (&lt;b>5&lt;/b>); and four lanostane-type triterpenoids, and three cyclic dipeptides (&lt;b>10&lt;/b>-&lt;b>12&lt;/b>), in addition to orcinol (&lt;b>13&lt;/b>), were isolated from the rice-based cultivation medium of &lt;i>H. erinaceus&lt;/i>. Their structures were determined by NMR, HR-ESI-MS, ECD, and calculated NMR. Compound &lt;b>1&lt;/b> marks a pioneering dis</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Aug</publication><modification>2026-04-08T15:14:17.227Z</modification><creation>2024-10-18T10:44:25.503Z</creation></dates><accession>S-EPMC10489798</accession><cross_references><pubmed>37687209</pubmed><doi>10.3390/molecules28176380</doi></cross_references></HashMap>