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Clerodane Diterpenoids from Callicarpa hypoleucophylla and Their Anti-Inflammatory Activity
Plants of the genus Callicarpa are known to possess several medicinal effects. The constituents of the Taiwan endemic plant Callicarpa hypoleucophylla have never been studied. Therefore, C. hypoleucophylla was selected for our phytochemical investigation. Two new clerodane-type diterpenoids, named c...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7287842/ https://www.ncbi.nlm.nih.gov/pubmed/32414033 http://dx.doi.org/10.3390/molecules25102288 |
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author | Lin, Yu-Chi Lin, Jue-Jun Chen, Shu-Rong Hwang, Tsong-Long Fang, Shu-Yen Korinek, Michal Chen, Ching-Yeu Lin, Yun-Sheng Wu, Tung-Ying Yen, Ming-Hong Wang, Chih-Hsin Cheng, Yuan-Bin |
author_facet | Lin, Yu-Chi Lin, Jue-Jun Chen, Shu-Rong Hwang, Tsong-Long Fang, Shu-Yen Korinek, Michal Chen, Ching-Yeu Lin, Yun-Sheng Wu, Tung-Ying Yen, Ming-Hong Wang, Chih-Hsin Cheng, Yuan-Bin |
author_sort | Lin, Yu-Chi |
collection | PubMed |
description | Plants of the genus Callicarpa are known to possess several medicinal effects. The constituents of the Taiwan endemic plant Callicarpa hypoleucophylla have never been studied. Therefore, C. hypoleucophylla was selected for our phytochemical investigation. Two new clerodane-type diterpenoids, named callihypolins A (1) and B (2), along with seven known compounds were isolated from the leaves and twigs of the Lamiaceae plant C. hypoleucophylla and then characterized. The structures of compounds 1 and 2 were elucidated by spectroscopic data analysis, specifically, two-dimension nuclear magnetic resonance (NMR). The anti-inflammatory activity of compounds 1–9 based on the suppression of superoxide anion generation and elastase release was evaluated. Among the isolates, compounds 2–4 showed anti-inflammatory activity (9.52−32.48% inhibition at the concentration 10 μm) by suppressing superoxide anion generation and elastase release. Our findings not only expand the description of the structural diversity of the compounds present in plants of the genus Callicarpa but also highlight the possibility of developing anti-inflammatory agents from Callicarpa endemic species. |
format | Online Article Text |
id | pubmed-7287842 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72878422020-06-15 Clerodane Diterpenoids from Callicarpa hypoleucophylla and Their Anti-Inflammatory Activity Lin, Yu-Chi Lin, Jue-Jun Chen, Shu-Rong Hwang, Tsong-Long Fang, Shu-Yen Korinek, Michal Chen, Ching-Yeu Lin, Yun-Sheng Wu, Tung-Ying Yen, Ming-Hong Wang, Chih-Hsin Cheng, Yuan-Bin Molecules Article Plants of the genus Callicarpa are known to possess several medicinal effects. The constituents of the Taiwan endemic plant Callicarpa hypoleucophylla have never been studied. Therefore, C. hypoleucophylla was selected for our phytochemical investigation. Two new clerodane-type diterpenoids, named callihypolins A (1) and B (2), along with seven known compounds were isolated from the leaves and twigs of the Lamiaceae plant C. hypoleucophylla and then characterized. The structures of compounds 1 and 2 were elucidated by spectroscopic data analysis, specifically, two-dimension nuclear magnetic resonance (NMR). The anti-inflammatory activity of compounds 1–9 based on the suppression of superoxide anion generation and elastase release was evaluated. Among the isolates, compounds 2–4 showed anti-inflammatory activity (9.52−32.48% inhibition at the concentration 10 μm) by suppressing superoxide anion generation and elastase release. Our findings not only expand the description of the structural diversity of the compounds present in plants of the genus Callicarpa but also highlight the possibility of developing anti-inflammatory agents from Callicarpa endemic species. MDPI 2020-05-13 /pmc/articles/PMC7287842/ /pubmed/32414033 http://dx.doi.org/10.3390/molecules25102288 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lin, Yu-Chi Lin, Jue-Jun Chen, Shu-Rong Hwang, Tsong-Long Fang, Shu-Yen Korinek, Michal Chen, Ching-Yeu Lin, Yun-Sheng Wu, Tung-Ying Yen, Ming-Hong Wang, Chih-Hsin Cheng, Yuan-Bin Clerodane Diterpenoids from Callicarpa hypoleucophylla and Their Anti-Inflammatory Activity |
title | Clerodane Diterpenoids from Callicarpa hypoleucophylla and Their Anti-Inflammatory Activity |
title_full | Clerodane Diterpenoids from Callicarpa hypoleucophylla and Their Anti-Inflammatory Activity |
title_fullStr | Clerodane Diterpenoids from Callicarpa hypoleucophylla and Their Anti-Inflammatory Activity |
title_full_unstemmed | Clerodane Diterpenoids from Callicarpa hypoleucophylla and Their Anti-Inflammatory Activity |
title_short | Clerodane Diterpenoids from Callicarpa hypoleucophylla and Their Anti-Inflammatory Activity |
title_sort | clerodane diterpenoids from callicarpa hypoleucophylla and their anti-inflammatory activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7287842/ https://www.ncbi.nlm.nih.gov/pubmed/32414033 http://dx.doi.org/10.3390/molecules25102288 |
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