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      Phytochemical Study of Stem and Leaf of Clausena lansium

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          Abstract

          Clausena lansium 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 C. lansium 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 C. lansium 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 Clausena, including a new aromatic glycoside ( 1), a new dihydrofuranocoumarin glycoside ( 6), and two new sesquiterpene glycosides ( 8 and 9). 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 C. lansium in the genus Clausena and suggests that some glycosides from this plant probably play a role in the anticancer activity of C. lansium to some extent.

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          NMR spectroscopy in the structural elucidation of oligosaccharides and glycosides.

          The potential of one- and two-dimensional NMR techniques for the identification of individual sugar residues, their anomeric configuration, interglycosidic linkages, sequencing and the site of any appended group, in establishing the structures of naturally occurring oligosaccharides and glycosides is presented.
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            Facile discrimination of aldose enantiomers by reversed-phase HPLC.

            One-pot reactions of aldoses with L-cysteine methyl ester and o-tolyl isothiocyanate yielded methyl 2-(polyhydroxyalkyl)-3-(o-tolylthiocarbamoyl)-thiazolidine-4(R)-carboxylates. Direct HPLC analysis of the reaction mixture and UV detection at 250 nm discriminated D- and L-enantiomers of aldoses. The reaction was applied to the determination of absolute configuration the sugar residues of an aroma precursor.
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              Antioxidative Phenolic Compounds from Sage (Salvia officinalis)

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                Author and article information

                Contributors
                Role: Academic Editor
                Role: Academic Editor
                Role: Academic Editor
                Journal
                Molecules
                Molecules
                molecules
                Molecules
                MDPI
                1420-3049
                28 August 2019
                September 2019
                : 24
                : 17
                : 3124
                Affiliations
                [1 ]Jiangxi Key Laboratory for Conservation and Utilization of Fungal Resources, Jiangxi Agricultural University, Nanchang 330045, China
                [2 ]College of Agriculture, Jiangxi Agricultural University, Nanchang 330045, China
                [3 ]School of Land Resources and Environment, Jiangxi Agricultural University, Nanchang 330045, China
                Author notes
                Article
                molecules-24-03124
                10.3390/molecules24173124
                6749519
                31466274
                5ccf4d85-13ca-4020-9735-bc70fcb7ea21
                © 2019 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/).

                History
                : 23 July 2019
                : 26 August 2019
                Categories
                Article

                clausena lansium,aromatic glycosides,sesquiterpene glycosides,dihydrofuranocoumarin glycosides

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