Rhodoterpenoids A‒C, Three New Rearranged Triterpenoids from Rhododendron latoucheae by HPLC‒MS‒SPE‒NMR
Abstract Rhodoterpenoids A‒C (1‒3), three new rearranged triterpenoids, together with one new biogenetically related compound, rhodoterpenoid D (4), were isolated and efficiently elucidated from Rhododendron latoucheae by high-performance liquid chromatography−mass spectrometry−solid-phase extractio...
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oai:doaj.org-article:7df32c212e6448dd9bbec9ffd9ef60212021-12-02T16:06:14ZRhodoterpenoids A‒C, Three New Rearranged Triterpenoids from Rhododendron latoucheae by HPLC‒MS‒SPE‒NMR10.1038/s41598-017-06320-x2045-2322https://doaj.org/article/7df32c212e6448dd9bbec9ffd9ef60212017-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-06320-xhttps://doaj.org/toc/2045-2322Abstract Rhodoterpenoids A‒C (1‒3), three new rearranged triterpenoids, together with one new biogenetically related compound, rhodoterpenoid D (4), were isolated and efficiently elucidated from Rhododendron latoucheae by high-performance liquid chromatography−mass spectrometry−solid-phase extraction−nuclear magnetic resonance (HPLC‒MS‒SPE‒NMR). Compounds 1 and 2 possess an unprecedented skeleton with a 5/7/6/6/6-fused pentacyclic ring system, while compound 3 contains a unique 6/7/6/6/6-fused pentacyclic carbon backbone. Their structures were determined by extensive spectroscopic methods and electronic circular dichroism (ECD) analyses. Plausible biogenetic pathways for 1‒4 were proposed. Compounds 1 and 4 showed potential activity against herpes simplex virus 1 (HSV-1) with IC50 values of 8.62 and 6.87 μM, respectively.Fei LiuYa-Nan WangYong LiShuang-Gang MaJing QuYun-Bao LiuChang-Shan NiuZhong-Hai TangTian-Tai ZhangYu-Huan LiLi LiShi-Shan YuNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-10 (2017) |
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Medicine R Science Q Fei Liu Ya-Nan Wang Yong Li Shuang-Gang Ma Jing Qu Yun-Bao Liu Chang-Shan Niu Zhong-Hai Tang Tian-Tai Zhang Yu-Huan Li Li Li Shi-Shan Yu Rhodoterpenoids A‒C, Three New Rearranged Triterpenoids from Rhododendron latoucheae by HPLC‒MS‒SPE‒NMR |
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Abstract Rhodoterpenoids A‒C (1‒3), three new rearranged triterpenoids, together with one new biogenetically related compound, rhodoterpenoid D (4), were isolated and efficiently elucidated from Rhododendron latoucheae by high-performance liquid chromatography−mass spectrometry−solid-phase extraction−nuclear magnetic resonance (HPLC‒MS‒SPE‒NMR). Compounds 1 and 2 possess an unprecedented skeleton with a 5/7/6/6/6-fused pentacyclic ring system, while compound 3 contains a unique 6/7/6/6/6-fused pentacyclic carbon backbone. Their structures were determined by extensive spectroscopic methods and electronic circular dichroism (ECD) analyses. Plausible biogenetic pathways for 1‒4 were proposed. Compounds 1 and 4 showed potential activity against herpes simplex virus 1 (HSV-1) with IC50 values of 8.62 and 6.87 μM, respectively. |
format |
article |
author |
Fei Liu Ya-Nan Wang Yong Li Shuang-Gang Ma Jing Qu Yun-Bao Liu Chang-Shan Niu Zhong-Hai Tang Tian-Tai Zhang Yu-Huan Li Li Li Shi-Shan Yu |
author_facet |
Fei Liu Ya-Nan Wang Yong Li Shuang-Gang Ma Jing Qu Yun-Bao Liu Chang-Shan Niu Zhong-Hai Tang Tian-Tai Zhang Yu-Huan Li Li Li Shi-Shan Yu |
author_sort |
Fei Liu |
title |
Rhodoterpenoids A‒C, Three New Rearranged Triterpenoids from Rhododendron latoucheae by HPLC‒MS‒SPE‒NMR |
title_short |
Rhodoterpenoids A‒C, Three New Rearranged Triterpenoids from Rhododendron latoucheae by HPLC‒MS‒SPE‒NMR |
title_full |
Rhodoterpenoids A‒C, Three New Rearranged Triterpenoids from Rhododendron latoucheae by HPLC‒MS‒SPE‒NMR |
title_fullStr |
Rhodoterpenoids A‒C, Three New Rearranged Triterpenoids from Rhododendron latoucheae by HPLC‒MS‒SPE‒NMR |
title_full_unstemmed |
Rhodoterpenoids A‒C, Three New Rearranged Triterpenoids from Rhododendron latoucheae by HPLC‒MS‒SPE‒NMR |
title_sort |
rhodoterpenoids a‒c, three new rearranged triterpenoids from rhododendron latoucheae by hplc‒ms‒spe‒nmr |
publisher |
Nature Portfolio |
publishDate |
2017 |
url |
https://doaj.org/article/7df32c212e6448dd9bbec9ffd9ef6021 |
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