Phytochemical Study of Stem and Leaf of <i>Clausena lansium</i>

<i>Clausena lansium</i> Lour. Skeels (Rutaceae) is widely distributed in South China and has historically been used as a traditional medicine in local healthcare systems. Although the characteristic components (carbazole alkaloids and coumarins) of <i>C. lansium</i> have been...

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Main Authors: Wenwen Peng, Xiaoxiang Fu, Yuyan Li, Zhonghua Xiong, Xugen Shi, Fang Zhang, Guanghua Huo, Baotong Li
Format: Article
Language:English
Published: MDPI AG 2019-08-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/24/17/3124
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author Wenwen Peng
Xiaoxiang Fu
Yuyan Li
Zhonghua Xiong
Xugen Shi
Fang Zhang
Guanghua Huo
Baotong Li
author_facet Wenwen Peng
Xiaoxiang Fu
Yuyan Li
Zhonghua Xiong
Xugen Shi
Fang Zhang
Guanghua Huo
Baotong Li
author_sort Wenwen Peng
collection DOAJ
description <i>Clausena lansium</i> Lour. Skeels (Rutaceae) is widely distributed in South China and has historically been used as a traditional medicine in local healthcare systems. Although the characteristic components (carbazole alkaloids and coumarins) of <i>C. lansium</i> have been found to possess a wide variety of biological activities, little attention has been paid toward the other components of this plant. In the current study, phytochemical analysis of isolates from a water-soluble stem and leaf extract of <i>C. lansium</i> led to the identification of 12 compounds, including five aromatic glycosides, four sesquiterpene glycosides, two dihydrofuranocoumarin glycosides, and one adenosine. All compounds were isolated for the first time from the genus <i>Clausena</i>, including a new aromatic glycoside (<b>1</b>), a new dihydrofuranocoumarin glycoside (<b>6</b>), and two new sesquiterpene glycosides (<b>8</b> and <b>9</b>). The phytochemical structures of the isolates were elucidated using spectroscopic analyses including NMR and MS. The existence of these compounds demonstrates the taxonomic significance of <i>C. lansium</i> in the genus <i>Clausena</i> and suggests that some glycosides from this plant probably play a role in the anticancer activity of <i>C. lansium</i> to some extent.
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spelling doaj.art-6e0959f362f84505bd6c9a137aa390282022-12-22T00:13:43ZengMDPI AGMolecules1420-30492019-08-012417312410.3390/molecules24173124molecules24173124Phytochemical Study of Stem and Leaf of <i>Clausena lansium</i>Wenwen Peng0Xiaoxiang Fu1Yuyan Li2Zhonghua Xiong3Xugen Shi4Fang Zhang5Guanghua Huo6Baotong Li7Jiangxi Key Laboratory for Conservation and Utilization of Fungal Resources, Jiangxi Agricultural University, Nanchang 330045, ChinaCollege of Agriculture, Jiangxi Agricultural University, Nanchang 330045, ChinaCollege of Agriculture, Jiangxi Agricultural University, Nanchang 330045, ChinaCollege of Agriculture, Jiangxi Agricultural University, Nanchang 330045, ChinaCollege of Agriculture, Jiangxi Agricultural University, Nanchang 330045, ChinaCollege of Agriculture, Jiangxi Agricultural University, Nanchang 330045, ChinaJiangxi Key Laboratory for Conservation and Utilization of Fungal Resources, Jiangxi Agricultural University, Nanchang 330045, ChinaSchool of Land Resources and Environment, Jiangxi Agricultural University, Nanchang 330045, China<i>Clausena lansium</i> Lour. Skeels (Rutaceae) is widely distributed in South China and has historically been used as a traditional medicine in local healthcare systems. Although the characteristic components (carbazole alkaloids and coumarins) of <i>C. lansium</i> have been found to possess a wide variety of biological activities, little attention has been paid toward the other components of this plant. In the current study, phytochemical analysis of isolates from a water-soluble stem and leaf extract of <i>C. lansium</i> led to the identification of 12 compounds, including five aromatic glycosides, four sesquiterpene glycosides, two dihydrofuranocoumarin glycosides, and one adenosine. All compounds were isolated for the first time from the genus <i>Clausena</i>, including a new aromatic glycoside (<b>1</b>), a new dihydrofuranocoumarin glycoside (<b>6</b>), and two new sesquiterpene glycosides (<b>8</b> and <b>9</b>). The phytochemical structures of the isolates were elucidated using spectroscopic analyses including NMR and MS. The existence of these compounds demonstrates the taxonomic significance of <i>C. lansium</i> in the genus <i>Clausena</i> and suggests that some glycosides from this plant probably play a role in the anticancer activity of <i>C. lansium</i> to some extent.https://www.mdpi.com/1420-3049/24/17/3124<i>Clausena lansium</i>aromatic glycosidessesquiterpene glycosidesdihydrofuranocoumarin glycosides
spellingShingle Wenwen Peng
Xiaoxiang Fu
Yuyan Li
Zhonghua Xiong
Xugen Shi
Fang Zhang
Guanghua Huo
Baotong Li
Phytochemical Study of Stem and Leaf of <i>Clausena lansium</i>
Molecules
<i>Clausena lansium</i>
aromatic glycosides
sesquiterpene glycosides
dihydrofuranocoumarin glycosides
title Phytochemical Study of Stem and Leaf of <i>Clausena lansium</i>
title_full Phytochemical Study of Stem and Leaf of <i>Clausena lansium</i>
title_fullStr Phytochemical Study of Stem and Leaf of <i>Clausena lansium</i>
title_full_unstemmed Phytochemical Study of Stem and Leaf of <i>Clausena lansium</i>
title_short Phytochemical Study of Stem and Leaf of <i>Clausena lansium</i>
title_sort phytochemical study of stem and leaf of i clausena lansium i
topic <i>Clausena lansium</i>
aromatic glycosides
sesquiterpene glycosides
dihydrofuranocoumarin glycosides
url https://www.mdpi.com/1420-3049/24/17/3124
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