<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Xu Y</submitter><pubmed_abstract>One new (&lt;b>1&lt;/b>) and fifteen known (&lt;b>2&lt;/b>-&lt;b>16&lt;/b>) &lt;i>p&lt;/i>-terphenyls were isolated from a solid culture of the endophytic fungus &lt;i>Aspergillus&lt;/i> sp. GZWMJZ-055 by adding the leaves of its host &lt;i>Eucommia ulmoides&lt;/i>. Furthermore, nine &lt;i>p&lt;/i>-terphenyls (&lt;b>17&lt;/b>-&lt;b>25&lt;/b>) were synthesized from the main compounds (&lt;b>5&lt;/b>-&lt;b>7&lt;/b>), among which derivatives &lt;b>18&lt;/b>, &lt;b>19&lt;/b>, &lt;b>21&lt;/b>, &lt;b>22&lt;/b>, and &lt;b>25&lt;/b> are new &lt;i>p&lt;/i>-terphenyls. Compounds &lt;b>15&lt;/b> and &lt;b>16&lt;/b> were also, respectively, synthesized from compounds &lt;b>6&lt;/b> and &lt;b>7&lt;/b> by oxidative cyclization of air in the presence of silica gel. These &lt;i>p&lt;/i>-terphenyls especially those with 4,2',4″-trihydroxy (&lt;b>4&lt;/b>-&lt;b>7&lt;/b>, &lt;b>20&lt;/b>, &lt;b>21&lt;/b>) or 4, 4″-dihydroxy-1,2,1',2'-furan (&lt;b>15&lt;/b>, &lt;b>16&lt;/b>) substituted nucleus, exhibited significant antioxidant and α-glucosidase inhibitory activities and lower cytotoxicity to caco-2 cells. The results indicated their potential use as lead compounds or dietary supplements for treating or preventing the diabetes.</pubmed_abstract><journal>Frontiers in microbiology</journal><pagination>654963</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7947296</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>&lt;i>p&lt;/i>-Terphenyls From &lt;i>Aspergillus&lt;/i> sp. GZWMJZ-055: Identification, Derivation, Antioxidant and α-Glycosidase Inhibitory Activities.</pubmed_title><pmcid>PMC7947296</pmcid><pubmed_authors>He W</pubmed_authors><pubmed_authors>Wu D</pubmed_authors><pubmed_authors>Zhu W</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Xu Y</pubmed_authors><pubmed_authors>Wang L</pubmed_authors></additional><is_claimable>false</is_claimable><name>&lt;i>p&lt;/i>-Terphenyls From &lt;i>Aspergillus&lt;/i> sp. GZWMJZ-055: Identification, Derivation, Antioxidant and α-Glycosidase Inhibitory Activities.</name><description>One new (&lt;b>1&lt;/b>) and fifteen known (&lt;b>2&lt;/b>-&lt;b>16&lt;/b>) &lt;i>p&lt;/i>-terphenyls were isolated from a solid culture of the endophytic fungus &lt;i>Aspergillus&lt;/i> sp. GZWMJZ-055 by adding the leaves of its host &lt;i>Eucommia ulmoides&lt;/i>. Furthermore, nine &lt;i>p&lt;/i>-terphenyls (&lt;b>17&lt;/b>-&lt;b>25&lt;/b>) were synthesized from the main compounds (&lt;b>5&lt;/b>-&lt;b>7&lt;/b>), among which derivatives &lt;b>18&lt;/b>, &lt;b>19&lt;/b>, &lt;b>21&lt;/b>, &lt;b>22&lt;/b>, and &lt;b>25&lt;/b> are new &lt;i>p&lt;/i>-terphenyls. Compounds &lt;b>15&lt;/b> and &lt;b>16&lt;/b> were also, respectively, synthesized from compounds &lt;b>6&lt;/b> and &lt;b>7&lt;/b> by oxidative cyclization of air in the presence of silica gel. These &lt;i>p&lt;/i>-terphenyls especially those with 4,2',4″-trihydroxy (&lt;b>4&lt;/b>-&lt;b>7&lt;/b>, &lt;b>20&lt;/b>, &lt;b>21&lt;/b>) or 4, 4″-dihydroxy-1,2,1',2'-furan (&lt;b>15&lt;/b>, &lt;b>16&lt;/b>) substituted nucleus, exhibited significant antioxidant and α-glucosidase inhibitory activities and lower cytotoxicity to caco-2 cells. The results indicated their potential use as lead compounds or dietary supplements for treating or preventing the diabetes.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2024-12-04T07:39:25.084Z</modification><creation>2021-03-14T08:21:06Z</creation></dates><accession>S-EPMC7947296</accession><cross_references><pubmed>33717048</pubmed><doi>10.3389/fmicb.2021.654963</doi></cross_references></HashMap>