<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ngoc Mai TT</submitter><funding>Vietnam Academy of Science and Technology</funding><pagination>12081-12095</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11019407</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(17)</volume><pubmed_abstract>Twelve compounds were isolated from &lt;i>Mussaenda saigonensis&lt;/i> aerial parts through phytochemical analysis and the genus &lt;i>Mussaenda&lt;/i> is the first place where the compounds 4-6 and 11-12 have been found. Based on the ability to inhibit NO production in RAW264.7 cells, compound 2 has demonstrated the strongest anti-inflammatory activity &lt;i>in vitro&lt;/i> with an IC&lt;sub>50&lt;/sub> of 7.6 μM, as opposed to L-NMMA's IC&lt;sub>50&lt;/sub> of 41.3 μM. Compound 12 was found to be the most effective inhibitor of alpha-glucosidase enzyme &lt;i>in vitro&lt;/i>, with an IC&lt;sub>50&lt;/sub> value of 42.4 μM (compared to 168 μM for acarbose). Compounds 1-12 were evaluated &lt;i>in vitro&lt;/i> for antimicrobial activity using the paper dish method. Compound 11 demonstrated strong antifungal activity against &lt;i>M. gypseum&lt;</pubmed_abstract><journal>RSC advances</journal><pubmed_title>&lt;i>In vitro&lt;/i> and &lt;i>in silico&lt;/i> docking and molecular dynamic of antimicrobial activities, alpha-glucosidase, and anti-inflammatory activity of compounds from the aerial parts of &lt;i>Mussaenda saigonensis&lt;/i>.</pubmed_title><pmcid>PMC11019407</pmcid><funding_grant_id>NCVCC15.02/22-23</funding_grant_id><pubmed_authors>Minh An TN</pubmed_authors><pubmed_authors>Hong Anh NT</pubmed_authors><pubmed_authors>Ngoc Mai TT</pubmed_authors><pubmed_authors>Tri MD</pubmed_authors><pubmed_authors>Minh PN</pubmed_authors><pubmed_authors>Nhi Phan NH</pubmed_authors><pubmed_authors>Dang VS</pubmed_authors><pubmed_authors>Van Hue N</pubmed_authors><pubmed_authors>Phat NT</pubmed_authors><pubmed_authors>Chi MT</pubmed_authors><pubmed_authors>Duong TH</pubmed_authors></additional><is_claimable>false</is_claimable><name>&lt;i>In vitro&lt;/i> and &lt;i>in silico&lt;/i> docking and molecular dynamic of antimicrobial activities, alpha-glucosidase, and anti-inflammatory activity of compounds from the aerial parts of &lt;i>Mussaenda saigonensis&lt;/i>.</name><description>Twelve compounds were isolated from &lt;i>Mussaenda saigonensis&lt;/i> aerial parts through phytochemical analysis and the genus &lt;i>Mussaenda&lt;/i> is the first place where the compounds 4-6 and 11-12 have been found. Based on the ability to inhibit NO production in RAW264.7 cells, compound 2 has demonstrated the strongest anti-inflammatory activity &lt;i>in vitro&lt;/i> with an IC&lt;sub>50&lt;/sub> of 7.6 μM, as opposed to L-NMMA's IC&lt;sub>50&lt;/sub> of 41.3 μM. Compound 12 was found to be the most effective inhibitor of alpha-glucosidase enzyme &lt;i>in vitro&lt;/i>, with an IC&lt;sub>50&lt;/sub> value of 42.4 μM (compared to 168 μM for acarbose). Compounds 1-12 were evaluated &lt;i>in vitro&lt;/i> for antimicrobial activity using the paper dish method. Compound 11 demonstrated strong antifungal activity against &lt;i>M. gypseum&lt;</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2026-06-02T10:26:19.496Z</modification><creation>2025-04-06T00:48:43.06Z</creation></dates><accession>S-EPMC11019407</accession><cross_references><pubmed>38628478</pubmed><doi>10.1039/d4ra01865f</doi></cross_references></HashMap>