Quercetin -3-O-β-D-glucouronide butyl ester from Vitis vinifera leaves of potent anti-helicobacter pylori activity and impact of its combination with clarithromycin | ||||
Egyptian Journal of Chemistry | ||||
Article 58, Volume 65, Issue 10, October 2022, Page 609-615 PDF (574.73 K) | ||||
Document Type: Original Article | ||||
DOI: 10.21608/ejchem.2022.106639.4896 | ||||
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Authors | ||||
Mohamed Elraey ![]() ![]() | ||||
1National Research centre | ||||
2Department of Chemistry of Natural and microbial products, Pharmaceutical institute, National Research Centre, Dokki, Cairo, Egypt | ||||
3Department of Chemistry of Natural Compounds, Pharmaceutical Division, National Research Centre, Dokki, Cairo, Egypt, | ||||
Abstract | ||||
Antibiotic resistance by Helicobacter pylori has reduced the eradication rates of multiple therapies. To overcome this crisis, we select safe nutraceutical derived agents of low price for investigation. The hydroalcholic extract of Vitis vinifera leaves beside the isolated compounds; quercetin-3-O-β-D-glucouronide (CPD1) beside its butyl ester (CPD2) which was isolated first time of the plant were investigated against six clarithromycin resistant isolated strains of H.pylori. Combination between the antibiotic clarithromycin and extract, CPD1 and CPD2 were also carried out. The hydroalcoholic extract, CPD1 and CPD2 showed distinctive inhibition zones of the growth of H.pylori in comparison to clarithromycin. CPD2 only showed synergistic effect on combination with clarithromycin. The mechanism of action was studied virtually against H. pylori HyPB and showed docking scores -7.26 and -6.89 Kcal for CPD1 and CPD2 respectively, which mean that both compounds affects colonization of H. pylori and in turn prevent formation of new generations of H.pylori. | ||||
Keywords | ||||
: Vitis vinifera; Quercetin -3-O- β -D-glucouronide butyl ester; Helicobacter pylori; Molecular Docking; Helicobacter pylori HypB protein | ||||
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