<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>47(6)</volume><submitter>Hong SS</submitter><pubmed_abstract>&lt;i>Veratrum&lt;/i> spp. have traditionally been used in folk medicine to treat various pathologies. In this study, nine compounds, comprising one simple phenolic compound (&lt;b>1&lt;/b>), three stilbenoids (&lt;b>2&lt;/b>-&lt;b>4&lt;/b>), and five flavonoids (&lt;b>5&lt;/b>-&lt;b>9&lt;/b>), were isolated from the aerial parts of &lt;i>Veratrum versicolor&lt;/i> f. &lt;i>viride&lt;/i> Nakai. The structures of these compounds were elucidated by spectroscopic analyses and comparison with reported data. Together, all reported compounds were isolated from &lt;i>V. versicolor&lt;/i> f. &lt;i>viride&lt;/i> for the first time in the study. Among them, two flavone aglycone tricetins (&lt;b>7&lt;/b> and &lt;b>9&lt;/b>) have never been isolated from the genus &lt;i>Veratrum&lt;/i> or the family Melanthiaceae. The ethanol extract and isolated compounds were assessed for their inhibitory effects on elastase, tyrosinase, and melanin synthesis. Compounds &lt;b>5&lt;/b> and &lt;b>7&lt;/b> inhibited elastase (IC&lt;sub>50&lt;/sub>: 292.25 ± 14.39 and 800.41 ± 5.86 μM, respectively), whereas compounds &lt;b>2&lt;/b>-&lt;b>5&lt;/b> inhibited tyrosinase with IC&lt;sub>50&lt;/sub> values in the range of 6.42 ~ 51.19 μM, respectively. In addition, compounds &lt;b>3&lt;/b>-&lt;b>6&lt;/b> and &lt;b>8&lt;/b> exhibited dose-dependent inhibition (70.4% ~ 91.0%) of melanogenesis at a concentration of 100 μM.</pubmed_abstract><journal>Turkish journal of chemistry</journal><pagination>1346-1354</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10965189</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Phytochemical investigation on the aerial parts of &lt;i>Veratrum versicolor&lt;/i> f. &lt;i>viride&lt;/i> Nakai and their biological activities.</pubmed_title><pmcid>PMC10965189</pmcid><pubmed_authors>Choi CW</pubmed_authors><pubmed_authors>Jeong YW</pubmed_authors><pubmed_authors>Lee JE</pubmed_authors><pubmed_authors>Jeong W</pubmed_authors><pubmed_authors>Choi YH</pubmed_authors><pubmed_authors>Hong SS</pubmed_authors><pubmed_authors>Ahn EK</pubmed_authors><pubmed_authors>Oh JS</pubmed_authors><pubmed_authors>Lee JY</pubmed_authors><pubmed_authors>Ahn IH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Phytochemical investigation on the aerial parts of &lt;i>Veratrum versicolor&lt;/i> f. &lt;i>viride&lt;/i> Nakai and their biological activities.</name><description>&lt;i>Veratrum&lt;/i> spp. have traditionally been used in folk medicine to treat various pathologies. In this study, nine compounds, comprising one simple phenolic compound (&lt;b>1&lt;/b>), three stilbenoids (&lt;b>2&lt;/b>-&lt;b>4&lt;/b>), and five flavonoids (&lt;b>5&lt;/b>-&lt;b>9&lt;/b>), were isolated from the aerial parts of &lt;i>Veratrum versicolor&lt;/i> f. &lt;i>viride&lt;/i> Nakai. The structures of these compounds were elucidated by spectroscopic analyses and comparison with reported data. Together, all reported compounds were isolated from &lt;i>V. versicolor&lt;/i> f. &lt;i>viride&lt;/i> for the first time in the study. Among them, two flavone aglycone tricetins (&lt;b>7&lt;/b> and &lt;b>9&lt;/b>) have never been isolated from the genus &lt;i>Veratrum&lt;/i> or the family Melanthiaceae. The ethanol extract and isolated compounds were assessed for their inhibitory effects on elastase, tyrosinase, and melanin synthesis. Compounds &lt;b>5&lt;/b> and &lt;b>7&lt;/b> inhibited elastase (IC&lt;sub>50&lt;/sub>: 292.25 ± 14.39 and 800.41 ± 5.86 μM, respectively), whereas compounds &lt;b>2&lt;/b>-&lt;b>5&lt;/b> inhibited tyrosinase with IC&lt;sub>50&lt;/sub> values in the range of 6.42 ~ 51.19 μM, respectively. In addition, compounds &lt;b>3&lt;/b>-&lt;b>6&lt;/b> and &lt;b>8&lt;/b> exhibited dose-dependent inhibition (70.4% ~ 91.0%) of melanogenesis at a concentration of 100 μM.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-04T23:53:49.461Z</modification><creation>2025-04-04T23:53:49.461Z</creation></dates><accession>S-EPMC10965189</accession><cross_references><pubmed>38544705</pubmed><doi>10.55730/1300-0527.3618</doi></cross_references></HashMap>