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Benzophenone Rhamnosides and Chromones from Hypericum seniawinii Maxim.
Two new benzophenone glycosides, hypersens A and B, along with four known compounds, (S)-(+)-5,7-dihydroxy-2-(1-methylpropyl) chromone (3), 5,7-dihydroxy-2-isopropylchromone (4), urachromone B (5), and 3-8′′ bisapigenin (6), were isolated from Hypericum seniawinii. The structures of new compounds (1...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9609419/ https://www.ncbi.nlm.nih.gov/pubmed/36296651 http://dx.doi.org/10.3390/molecules27207056 |
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author | Xia, Jing Hu, Bo Qian, Mengyu Zhang, Jiayue Wu, Lin |
author_facet | Xia, Jing Hu, Bo Qian, Mengyu Zhang, Jiayue Wu, Lin |
author_sort | Xia, Jing |
collection | PubMed |
description | Two new benzophenone glycosides, hypersens A and B, along with four known compounds, (S)-(+)-5,7-dihydroxy-2-(1-methylpropyl) chromone (3), 5,7-dihydroxy-2-isopropylchromone (4), urachromone B (5), and 3-8′′ bisapigenin (6), were isolated from Hypericum seniawinii. The structures of new compounds (1 and 2) were elucidated according to comprehensive spectroscopic data analyses. The absolute configurations of 1 and 2 were determined by electronic circular dichroism (ECD) calculations. All isolated compounds were evaluated for their neuroprotective effect using corticosterone-induced PC12 cell injury. In addition, compounds 1–6 were evaluated for their anti-inflammatory activity in lipopolysaccharide-induced RAW 264.7 cells. Compound 6 was a biflavonoid and significantly inhibited the production of nitric oxide with an IC(50) value of 11.48 ± 1.23 μM. |
format | Online Article Text |
id | pubmed-9609419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96094192022-10-28 Benzophenone Rhamnosides and Chromones from Hypericum seniawinii Maxim. Xia, Jing Hu, Bo Qian, Mengyu Zhang, Jiayue Wu, Lin Molecules Article Two new benzophenone glycosides, hypersens A and B, along with four known compounds, (S)-(+)-5,7-dihydroxy-2-(1-methylpropyl) chromone (3), 5,7-dihydroxy-2-isopropylchromone (4), urachromone B (5), and 3-8′′ bisapigenin (6), were isolated from Hypericum seniawinii. The structures of new compounds (1 and 2) were elucidated according to comprehensive spectroscopic data analyses. The absolute configurations of 1 and 2 were determined by electronic circular dichroism (ECD) calculations. All isolated compounds were evaluated for their neuroprotective effect using corticosterone-induced PC12 cell injury. In addition, compounds 1–6 were evaluated for their anti-inflammatory activity in lipopolysaccharide-induced RAW 264.7 cells. Compound 6 was a biflavonoid and significantly inhibited the production of nitric oxide with an IC(50) value of 11.48 ± 1.23 μM. MDPI 2022-10-19 /pmc/articles/PMC9609419/ /pubmed/36296651 http://dx.doi.org/10.3390/molecules27207056 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 Xia, Jing Hu, Bo Qian, Mengyu Zhang, Jiayue Wu, Lin Benzophenone Rhamnosides and Chromones from Hypericum seniawinii Maxim. |
title | Benzophenone Rhamnosides and Chromones from Hypericum seniawinii Maxim. |
title_full | Benzophenone Rhamnosides and Chromones from Hypericum seniawinii Maxim. |
title_fullStr | Benzophenone Rhamnosides and Chromones from Hypericum seniawinii Maxim. |
title_full_unstemmed | Benzophenone Rhamnosides and Chromones from Hypericum seniawinii Maxim. |
title_short | Benzophenone Rhamnosides and Chromones from Hypericum seniawinii Maxim. |
title_sort | benzophenone rhamnosides and chromones from hypericum seniawinii maxim. |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9609419/ https://www.ncbi.nlm.nih.gov/pubmed/36296651 http://dx.doi.org/10.3390/molecules27207056 |
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