<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jiang S</submitter><funding>Yunnan Revitalization Talent Support Program "Young Talent" Project</funding><funding>Yunnan Province Science and Technology Department</funding><funding>National Natural Science Foundation of China</funding><pagination>1581</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11013477</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>29(7)</volume><pubmed_abstract>A novel &lt;i>Lycopodium&lt;/i> alkaloid, lycocasine A (&lt;b>1&lt;/b>), and seven known &lt;i>Lycopodium&lt;/i> alkaloids (&lt;b>2&lt;/b>-&lt;b>8&lt;/b>), were isolated from &lt;i>Lycopodiastrum casuarinoides&lt;/i>. Their structures were determined through NMR, HRESIMS, and X-ray diffraction analysis. Compound &lt;b>1&lt;/b> features an unprecedented 5/6/6 tricyclic skeleton, highlighted by a 5-aza-tricyclic[6,3,1,0&lt;sup>2,6&lt;/sup>]dodecane motif. In bioactivity assays, compound &lt;b>1&lt;/b> demonstrated weak inhibitory activity against acid-sensing ion channel 1a.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Lycocasine A, a &lt;i>Lycopodium&lt;/i> Alkaloid from &lt;i>Lycopodiastrum casuarinoides&lt;/i> and Its Acid-Sensing Ion Channel 1a Inhibitory Activity.</pubmed_title><pmcid>PMC11013477</pmcid><funding_grant_id>NO</funding_grant_id><funding_grant_id>21837003</funding_grant_id><funding_grant_id>202305AH340005</funding_grant_id><pubmed_authors>Zhao QS</pubmed_authors><pubmed_authors>Jiang S</pubmed_authors><pubmed_authors>Li WY</pubmed_authors><pubmed_authors>Gao BB</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lycocasine A, a &lt;i>Lycopodium&lt;/i> Alkaloid from &lt;i>Lycopodiastrum casuarinoides&lt;/i> and Its Acid-Sensing Ion Channel 1a Inhibitory Activity.</name><description>A novel &lt;i>Lycopodium&lt;/i> alkaloid, lycocasine A (&lt;b>1&lt;/b>), and seven known &lt;i>Lycopodium&lt;/i> alkaloids (&lt;b>2&lt;/b>-&lt;b>8&lt;/b>), were isolated from &lt;i>Lycopodiastrum casuarinoides&lt;/i>. Their structures were determined through NMR, HRESIMS, and X-ray diffraction analysis. Compound &lt;b>1&lt;/b> features an unprecedented 5/6/6 tricyclic skeleton, highlighted by a 5-aza-tricyclic[6,3,1,0&lt;sup>2,6&lt;/sup>]dodecane motif. In bioactivity assays, compound &lt;b>1&lt;/b> demonstrated weak inhibitory activity against acid-sensing ion channel 1a.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2024-11-12T11:16:55.555Z</modification><creation>2024-11-12T11:16:55.555Z</creation></dates><accession>S-EPMC11013477</accession><cross_references><pubmed>38611859</pubmed><doi>10.3390/molecules29071581</doi></cross_references></HashMap>