1983
DOI: 10.1055/s-2007-969908
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Chemistry,13C-NMR Study and Pharmacology of Two Saponins from Colubrina asiatica

Abstract: From the leaves of COLUBRINA ASIATICA B RONGEN (Rhamnaceae) two saponins have been isolated and structurally elucidated, mainly by (13)C-NMR-spectroscopic methods, as jujubogenin-3-O-[2-O-acetyl-3-O-(3-O-beta-D-xylopyranosyl-4-O-acetyl-beta-D-glucopyranosyl)-alpha-L-arabinoside] (colubrinoside) and jujubogenin-3-O- [2-O-acetyl -3-O- (2-O- beta -D- xylopyranosyl-beta-D-glucopyranosyl)-alpha-L-arabinoside] (colubrin) respectively. Both saponins inhibit the spontaneous motility of mice, even at low doses (1 mg/ k… Show more

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Cited by 46 publications
(37 citation statements)
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(13 reference statements)
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“…It has been reported that quercetin and kaempferol possess anxiolytic and sedative activities (AguirreHernández et al, 2010;Jäger and Saaby, 2011). Saponins are also found to exhibit sedative activity (Wagner et al, 1983). Considering our results and previously published reports, it can be suggested that the anxiolytic and sedative activities observed for the plant extract might be due to the presence of CNS active compounds.…”
Section: Resultssupporting
confidence: 78%
“…It has been reported that quercetin and kaempferol possess anxiolytic and sedative activities (AguirreHernández et al, 2010;Jäger and Saaby, 2011). Saponins are also found to exhibit sedative activity (Wagner et al, 1983). Considering our results and previously published reports, it can be suggested that the anxiolytic and sedative activities observed for the plant extract might be due to the presence of CNS active compounds.…”
Section: Resultssupporting
confidence: 78%
“…Flavonoids and their related compounds also exhibit inhibition of arachidonic acid peroxidation, which results in reduction of prostaglandin levels thus reducing the fever and pain (Baumann et al, 1980). Saponins have been implicated in opioid receptor mechanism (Huong et al, 1995) through antagonistic activity (Wagner et al, 1983) by binding on the sensory nerve terminals. It suggests that flavonoids and saponins were responsible for the antipyretic and antinociceptive effects of N. latifolia roots decoction.…”
Section: Pharmaceutical Biologymentioning
confidence: 99%
“…Nevertheless, these compounds also exhibit a variety of pharmacological properties such as analgesic (Gene et al, 1996), antiulcerogenic (Wrzeciono et al, 1985), sedative (Wagner et al, 1983) and corticosterone secretion-induction properties (Yokoyama et al, 1982). In addition, a preliminary screening of the extracts from approximately 400 different plants led to the discovery of myricerone caffeoyl ester (1), a triterpene derivative isolated from a crude extract of twigs of the southern bayberry (Myrica cerifera), which showed high specificity for the human endothelin type A receptor (Fujimoto et al, 1992;Mihara and Fujimoto, 1993;Maguire et al, 1994).…”
Section: Introductionmentioning
confidence: 99%