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Anti-inflammatory Withanolides from Physalis minima

[Image: see text] Five new withanolides (1–5) along with five known ones (6–10) were isolated from the whole plants of Physalis minima Linn. The chemical structures of the new compounds were identified as (20S,22R) 15a-acetoxy-5β,6β-epoxy-4β,14a,28-trihydroxy-3β-methoxy-1-oxowitha-16,24-dienolide (1...

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Autores principales: Wu, Jiangping, Zhang, Tao, Yu, Meng, Jia, Hongmei, Zhang, Hongwu, Xu, Qiongming, Gu, Yucheng, Zou, Zhongmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7271383/
https://www.ncbi.nlm.nih.gov/pubmed/32548395
http://dx.doi.org/10.1021/acsomega.0c00467
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author Wu, Jiangping
Zhang, Tao
Yu, Meng
Jia, Hongmei
Zhang, Hongwu
Xu, Qiongming
Gu, Yucheng
Zou, Zhongmei
author_facet Wu, Jiangping
Zhang, Tao
Yu, Meng
Jia, Hongmei
Zhang, Hongwu
Xu, Qiongming
Gu, Yucheng
Zou, Zhongmei
author_sort Wu, Jiangping
collection PubMed
description [Image: see text] Five new withanolides (1–5) along with five known ones (6–10) were isolated from the whole plants of Physalis minima Linn. The chemical structures of the new compounds were identified as (20S,22R) 15a-acetoxy-5β,6β-epoxy-4β,14a,28-trihydroxy-3β-methoxy-1-oxowitha-16,24-dienolide (1), (20S,22R) 15a-acetoxy-5β,6β-epoxy-3β,4β,14β,17β,20β-pentahydroxy-1-oxowitha-24-enolide (2), (20R,22R) 15α-acetoxy-4β,5α,6β,14α,20β-pentahydroxy-1-oxowitha-2,24-dienolide (3), (20R,22R) 15α-acetoxy-5α,6β,14α,20β-tetrahydroxy-1-oxowitha-2,24-dienolide (4), and (20S,22R) 5α,6β,14β-trihydroxy-1,15-dioxowitha-2,16,24-trienolide (5) on the basis of integration combining IR, UV, HR-ESI-MS, 1D-NMR, and 2D-NMR analyses. Biologically, compounds (1–10) were subjected to evaluate their anti-inflammatory activities via inhibiting nitric oxide production in lipopolysaccharide-stimulated murine RAW 264.7 cells in vitro. The activity screening indicated that all of the compounds showed a moderate inhibitory effect against nitric oxide production with IC(50) values of 23.53–66.28 μM.
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spelling pubmed-72713832020-06-15 Anti-inflammatory Withanolides from Physalis minima Wu, Jiangping Zhang, Tao Yu, Meng Jia, Hongmei Zhang, Hongwu Xu, Qiongming Gu, Yucheng Zou, Zhongmei ACS Omega [Image: see text] Five new withanolides (1–5) along with five known ones (6–10) were isolated from the whole plants of Physalis minima Linn. The chemical structures of the new compounds were identified as (20S,22R) 15a-acetoxy-5β,6β-epoxy-4β,14a,28-trihydroxy-3β-methoxy-1-oxowitha-16,24-dienolide (1), (20S,22R) 15a-acetoxy-5β,6β-epoxy-3β,4β,14β,17β,20β-pentahydroxy-1-oxowitha-24-enolide (2), (20R,22R) 15α-acetoxy-4β,5α,6β,14α,20β-pentahydroxy-1-oxowitha-2,24-dienolide (3), (20R,22R) 15α-acetoxy-5α,6β,14α,20β-tetrahydroxy-1-oxowitha-2,24-dienolide (4), and (20S,22R) 5α,6β,14β-trihydroxy-1,15-dioxowitha-2,16,24-trienolide (5) on the basis of integration combining IR, UV, HR-ESI-MS, 1D-NMR, and 2D-NMR analyses. Biologically, compounds (1–10) were subjected to evaluate their anti-inflammatory activities via inhibiting nitric oxide production in lipopolysaccharide-stimulated murine RAW 264.7 cells in vitro. The activity screening indicated that all of the compounds showed a moderate inhibitory effect against nitric oxide production with IC(50) values of 23.53–66.28 μM. American Chemical Society 2020-05-17 /pmc/articles/PMC7271383/ /pubmed/32548395 http://dx.doi.org/10.1021/acsomega.0c00467 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Wu, Jiangping
Zhang, Tao
Yu, Meng
Jia, Hongmei
Zhang, Hongwu
Xu, Qiongming
Gu, Yucheng
Zou, Zhongmei
Anti-inflammatory Withanolides from Physalis minima
title Anti-inflammatory Withanolides from Physalis minima
title_full Anti-inflammatory Withanolides from Physalis minima
title_fullStr Anti-inflammatory Withanolides from Physalis minima
title_full_unstemmed Anti-inflammatory Withanolides from Physalis minima
title_short Anti-inflammatory Withanolides from Physalis minima
title_sort anti-inflammatory withanolides from physalis minima
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7271383/
https://www.ncbi.nlm.nih.gov/pubmed/32548395
http://dx.doi.org/10.1021/acsomega.0c00467
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