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Euphormins A and B, New Pyranocoumarin Derivatives from Euphorbia formosana Hayata, and Their Anti-Inflammatory Activity
Euphormin-A (1) and euphormin-B (2), two new pyranocoumarin derivatives, and forty known compounds (3–42) were isolated from Euphorbia formosana Hayata (Euphorbiaceae). The chemical structures of all compounds were established based on spectroscopic analyses. Several isolates were evaluated for thei...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8954059/ https://www.ncbi.nlm.nih.gov/pubmed/35335252 http://dx.doi.org/10.3390/molecules27061885 |
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author | Lan, Yu-Hsuan Chen, I-Hsiao Lu, Hsin-Hung Guo, Ting-Jing Hwang, Tsong-Long Leu, Yann-Lii |
author_facet | Lan, Yu-Hsuan Chen, I-Hsiao Lu, Hsin-Hung Guo, Ting-Jing Hwang, Tsong-Long Leu, Yann-Lii |
author_sort | Lan, Yu-Hsuan |
collection | PubMed |
description | Euphormin-A (1) and euphormin-B (2), two new pyranocoumarin derivatives, and forty known compounds (3–42) were isolated from Euphorbia formosana Hayata (Euphorbiaceae). The chemical structures of all compounds were established based on spectroscopic analyses. Several isolates were evaluated for their anti-inflammatory activity. Compounds 1, 2, 10, 18, 25, and 33 significantly inhibited against superoxide anion generation and elastase release by human neutrophils in response to formyl-L-methionyl-L-leucyl-L-phenylalanine/cytochalasin B (fMLP/CB). Furthermore, compounds 25 and 33 displayed the most potent effects with IC(50) values of 0.68 ± 0.18 and 1.39 ± 0.12 µM, respectively, against superoxide anion generation when compared with the positive control (2.01 ± 0.06 µM). |
format | Online Article Text |
id | pubmed-8954059 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89540592022-03-26 Euphormins A and B, New Pyranocoumarin Derivatives from Euphorbia formosana Hayata, and Their Anti-Inflammatory Activity Lan, Yu-Hsuan Chen, I-Hsiao Lu, Hsin-Hung Guo, Ting-Jing Hwang, Tsong-Long Leu, Yann-Lii Molecules Article Euphormin-A (1) and euphormin-B (2), two new pyranocoumarin derivatives, and forty known compounds (3–42) were isolated from Euphorbia formosana Hayata (Euphorbiaceae). The chemical structures of all compounds were established based on spectroscopic analyses. Several isolates were evaluated for their anti-inflammatory activity. Compounds 1, 2, 10, 18, 25, and 33 significantly inhibited against superoxide anion generation and elastase release by human neutrophils in response to formyl-L-methionyl-L-leucyl-L-phenylalanine/cytochalasin B (fMLP/CB). Furthermore, compounds 25 and 33 displayed the most potent effects with IC(50) values of 0.68 ± 0.18 and 1.39 ± 0.12 µM, respectively, against superoxide anion generation when compared with the positive control (2.01 ± 0.06 µM). MDPI 2022-03-14 /pmc/articles/PMC8954059/ /pubmed/35335252 http://dx.doi.org/10.3390/molecules27061885 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lan, Yu-Hsuan Chen, I-Hsiao Lu, Hsin-Hung Guo, Ting-Jing Hwang, Tsong-Long Leu, Yann-Lii Euphormins A and B, New Pyranocoumarin Derivatives from Euphorbia formosana Hayata, and Their Anti-Inflammatory Activity |
title | Euphormins A and B, New Pyranocoumarin Derivatives from Euphorbia formosana Hayata, and Their Anti-Inflammatory Activity |
title_full | Euphormins A and B, New Pyranocoumarin Derivatives from Euphorbia formosana Hayata, and Their Anti-Inflammatory Activity |
title_fullStr | Euphormins A and B, New Pyranocoumarin Derivatives from Euphorbia formosana Hayata, and Their Anti-Inflammatory Activity |
title_full_unstemmed | Euphormins A and B, New Pyranocoumarin Derivatives from Euphorbia formosana Hayata, and Their Anti-Inflammatory Activity |
title_short | Euphormins A and B, New Pyranocoumarin Derivatives from Euphorbia formosana Hayata, and Their Anti-Inflammatory Activity |
title_sort | euphormins a and b, new pyranocoumarin derivatives from euphorbia formosana hayata, and their anti-inflammatory activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8954059/ https://www.ncbi.nlm.nih.gov/pubmed/35335252 http://dx.doi.org/10.3390/molecules27061885 |
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