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New Cyclic Diarylheptanoids from Platycarya strobilacea

Five new cyclic diarylheptanoids (platycary A–E, compounds 1–5) and three previously identified analogues (i.e., phttyearynol (compound 6), myricatomentogenin (compound 7), and juglanin D (compound 8)) were isolated from the stem bark of Platycarya strobilacea. The structures of these compounds were...

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Autores principales: Ding, Wen-bing, Zhao, Rui-yuan, Li, Guan-hua, Liu, Bing-lei, He, Hua-liang, Qiu, Lin, Xue, Jin, Li, You-zhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7766178/
https://www.ncbi.nlm.nih.gov/pubmed/33419270
http://dx.doi.org/10.3390/molecules25246034
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author Ding, Wen-bing
Zhao, Rui-yuan
Li, Guan-hua
Liu, Bing-lei
He, Hua-liang
Qiu, Lin
Xue, Jin
Li, You-zhi
author_facet Ding, Wen-bing
Zhao, Rui-yuan
Li, Guan-hua
Liu, Bing-lei
He, Hua-liang
Qiu, Lin
Xue, Jin
Li, You-zhi
author_sort Ding, Wen-bing
collection PubMed
description Five new cyclic diarylheptanoids (platycary A–E, compounds 1–5) and three previously identified analogues (i.e., phttyearynol (compound 6), myricatomentogenin (compound 7), and juglanin D (compound 8)) were isolated from the stem bark of Platycarya strobilacea. The structures of these compounds were determined using NMR, HRESIMS, and electronic circular dichroism (ECD) data. The cytotoxicity of compounds 1–5 and their ability to inhibit nitric oxide (NO) production, as well as protect against the corticosterone-induced apoptosis of Pheochromocytoma (PC12) cells, were evaluated in vitro using the appropriate bioassays. Compounds 1 and 2 significantly inhibited the corticosterone-induced apoptosis of PC12 cells at a concentration of 20 μΜ.
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spelling pubmed-77661782020-12-28 New Cyclic Diarylheptanoids from Platycarya strobilacea Ding, Wen-bing Zhao, Rui-yuan Li, Guan-hua Liu, Bing-lei He, Hua-liang Qiu, Lin Xue, Jin Li, You-zhi Molecules Article Five new cyclic diarylheptanoids (platycary A–E, compounds 1–5) and three previously identified analogues (i.e., phttyearynol (compound 6), myricatomentogenin (compound 7), and juglanin D (compound 8)) were isolated from the stem bark of Platycarya strobilacea. The structures of these compounds were determined using NMR, HRESIMS, and electronic circular dichroism (ECD) data. The cytotoxicity of compounds 1–5 and their ability to inhibit nitric oxide (NO) production, as well as protect against the corticosterone-induced apoptosis of Pheochromocytoma (PC12) cells, were evaluated in vitro using the appropriate bioassays. Compounds 1 and 2 significantly inhibited the corticosterone-induced apoptosis of PC12 cells at a concentration of 20 μΜ. MDPI 2020-12-20 /pmc/articles/PMC7766178/ /pubmed/33419270 http://dx.doi.org/10.3390/molecules25246034 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
Ding, Wen-bing
Zhao, Rui-yuan
Li, Guan-hua
Liu, Bing-lei
He, Hua-liang
Qiu, Lin
Xue, Jin
Li, You-zhi
New Cyclic Diarylheptanoids from Platycarya strobilacea
title New Cyclic Diarylheptanoids from Platycarya strobilacea
title_full New Cyclic Diarylheptanoids from Platycarya strobilacea
title_fullStr New Cyclic Diarylheptanoids from Platycarya strobilacea
title_full_unstemmed New Cyclic Diarylheptanoids from Platycarya strobilacea
title_short New Cyclic Diarylheptanoids from Platycarya strobilacea
title_sort new cyclic diarylheptanoids from platycarya strobilacea
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7766178/
https://www.ncbi.nlm.nih.gov/pubmed/33419270
http://dx.doi.org/10.3390/molecules25246034
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