Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Xia, Jing, Hu, Bo, Qian, Mengyu, Zhang, Jiayue, Wu, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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
_version_ 1784819014398115840
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
work_keys_str_mv AT xiajing benzophenonerhamnosidesandchromonesfromhypericumseniawiniimaxim
AT hubo benzophenonerhamnosidesandchromonesfromhypericumseniawiniimaxim
AT qianmengyu benzophenonerhamnosidesandchromonesfromhypericumseniawiniimaxim
AT zhangjiayue benzophenonerhamnosidesandchromonesfromhypericumseniawiniimaxim
AT wulin benzophenonerhamnosidesandchromonesfromhypericumseniawiniimaxim