Abstract

The phytochemicals in the leaves of Cotoneaster mongolica Pojark, as well as their antioxidant and acetylcholinesterase (AChE) inhibitory activity were studied. The methanol extract of the leaves showed acetylcholinesterase inhibitory activity (IC50, 32.61 ± 0.51 μg/mL). The n-butanol fraction of this extract exhibited DPPH radical scavenging (IC50, 55.70 ± 0.15 μg/mL) and AChE inhibitory activity (IC50, 72.50 ± 0.60 μg/mL). From the n-butanol fraction quercetin (1), hyperoside (2), kaempferol-5-O-β-D-glucopyranoside (3), sissotrin (4), ursolic acid (5), corosolic acid (6), euscaphic acid (7), prunasin (8), (2R)-mandeloyl-β-D-glucopyranose (9), (Z)-3-hexenyl-O-α-L-rhamnopyranosyl-(1→6)-β-D-glucopyranoside (10), benzyl-O-α-L-rhamnopyranosyl-(1→6)-β-D-glucopyranoside (11) and arbutin (12) have been isolated and identified. Hyperoside, one of the major constituents among the isolated compounds, was active in both tested assays. Flavonol derivatives could provide the activity of this plant species.

Highlights

  • In the Mongolian flora, the genus Cotoneaster (Rosaceae) contains 4 represented species: C.mongolica

  • Shoots, twigs and leaves of Cotoneaster species as crude drugs are mainly used in the form of infusion, extract, tincture, tea and juice in traditional Mongolian medicine for the cure of intestinal inflammatory diseases, diarrhea, stomach indigestion, bowel disorders and abdominal cavity ascites, as well as rheumatoid arthritis

  • Cotoneaster species occurring in Russia, Iran, Uzbekistan, Turkey and Caucasia are used in traditional medicine, especially for the treatment of neurasthenia, nervous prostration, nasal hemorrhage, excessive menstruation, neonatal jaundice and cough [4,5,6]

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Summary

Introduction

In the Mongolian flora, the genus Cotoneaster (Rosaceae) contains 4 represented species: C.mongolica. No data were found on the biological activity of this plant species.In this study, phytochemicals in the leaves of C.mongolica, their antioxidant and acetylcholinesterase inhibitory activity were investigated. The absorbance was measured at 517 nm and the anti-oxidative activity (AA) was expressed in percentage: АA%=100- { [ (Abssample- Absblank) ×100] / Abscontrol}; Methanol (1.5 mL) added to the plant extract solution (1.5 mL) was used as a blank.

Results
Conclusion

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