<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yao WN</submitter><funding>Ministry of Education of the People&amp;apos;s Republic of China</funding><funding>National Natural Science Foundation of China</funding><funding>State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources, Guangxi Normal University</funding><pagination>2178-2183</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6044830</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>2(5)</volume><pubmed_abstract>Selagintamarlin A (&lt;b>1&lt;/b>), a novel selaginellin analogue featuring the unique motif of 1&lt;i>H&lt;/i>-2-benzopyran, a new selaginpulvilin E (&lt;b>2&lt;/b>), together with eight known analogues were isolated from &lt;i>Selaginella tamariscina&lt;/i>. Their structures were elucidated by extensive spectroscopic analyses. A plausible biosynthetic pathway of &lt;b>1&lt;/b> was also postulated. Compound &lt;b>1&lt;/b> showed remarkable inhibitory activity against phosphodiesterase-4 (PDE4D2), with an IC&lt;sub>50&lt;/sub> value of 40 nM, which is 20-fold higher than that of the positive control (rolipram). Furthermore, compound &lt;b>1&lt;/b> significantly inhibited tubulin polymerization.</pubmed_abstract><journal>ACS omega</journal><pubmed_title>Selagintamarlin A: A Selaginellin Analogue Possessing a 1&lt;i>H&lt;/i>-2-Benzopyran Core from &lt;i>Selaginella tamariscina&lt;/i>.</pubmed_title><pmcid>PMC6044830</pmcid><funding_grant_id>21431001</funding_grant_id><funding_grant_id>IRT_16R15</funding_grant_id><funding_grant_id>CMEMR2016-A02</funding_grant_id><funding_grant_id>81402817</funding_grant_id><funding_grant_id>20134504110002</funding_grant_id><pubmed_authors>Wang CG</pubmed_authors><pubmed_authors>Liang D</pubmed_authors><pubmed_authors>Hua J</pubmed_authors><pubmed_authors>Yao WN</pubmed_authors><pubmed_authors>Wang HS</pubmed_authors><pubmed_authors>Huang RZ</pubmed_authors><pubmed_authors>Zhang B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Selagintamarlin A: A Selaginellin Analogue Possessing a 1&lt;i>H&lt;/i>-2-Benzopyran Core from &lt;i>Selaginella tamariscina&lt;/i>.</name><description>Selagintamarlin A (&lt;b>1&lt;/b>), a novel selaginellin analogue featuring the unique motif of 1&lt;i>H&lt;/i>-2-benzopyran, a new selaginpulvilin E (&lt;b>2&lt;/b>), together with eight known analogues were isolated from &lt;i>Selaginella tamariscina&lt;/i>. Their structures were elucidated by extensive spectroscopic analyses. A plausible biosynthetic pathway of &lt;b>1&lt;/b> was also postulated. Compound &lt;b>1&lt;/b> showed remarkable inhibitory activity against phosphodiesterase-4 (PDE4D2), with an IC&lt;sub>50&lt;/sub> value of 40 nM, which is 20-fold higher than that of the positive control (rolipram). Furthermore, compound &lt;b>1&lt;/b> significantly inhibited tubulin polymerization.</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 May</publication><modification>2024-12-03T23:12:52.165Z</modification><creation>2019-03-26T23:47:33Z</creation></dates><accession>S-EPMC6044830</accession><cross_references><pubmed>30023657</pubmed><doi>10.1021/acsomega.7b00209</doi></cross_references></HashMap>