2012
DOI: 10.1007/s10068-012-0129-7
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Rapid identification of the α-glucosidase inhibitory compounds from Thunberg’s Geranium (Geranium thunbergii Sieb. et Zucc.)

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Cited by 15 publications
(6 citation statements)
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“…Two compounds with m/z 951 were detected at different retention time (Peak 38 and 50 ) which significantly differ in their fragmentation pattern, indicating the presence of isomeric structures which is common with ellagitannins. They were tentatively identified as granatin B and geraniin respectively [33, 34]. …”
Section: Discussionmentioning
confidence: 99%
“…Two compounds with m/z 951 were detected at different retention time (Peak 38 and 50 ) which significantly differ in their fragmentation pattern, indicating the presence of isomeric structures which is common with ellagitannins. They were tentatively identified as granatin B and geraniin respectively [33, 34]. …”
Section: Discussionmentioning
confidence: 99%
“…The α-glucosidase inhibitory activity of the extracts and fractions was determined using a modified procedure reported method with a slight modification [1]. The α-glucosidase activity was measured using the substrate p -nitrophenyl-α- d -glucopyranoside ( p NPG), which is hydrolyzed by α-glucosidase to release the product p -nitrophenol, a colorant that can be monitored at 405 nm.…”
Section: Methodsmentioning
confidence: 99%
“…One of the therapeutic approaches for counteracting hyperglycemia is to block the absorption of glucose by inhibiting the activity of carbohydrate-hydrolyzing enzymes such as α-glucosidase in the digestive organs. Small intestinal α-glucosidases (EC 3.2.1.20) are key enzymes involved in dietary carbohydrate digestion in humans [1]. Inhibitors of these enzymes may be effective in decreasing carbohydrate digestion and glucose absorption to suppress postprandial hyperglycemia [2].…”
Section: Introductionmentioning
confidence: 99%
“…α-Glucosidase inhibitory activity was determined using a previously reported method with slight modifications [ 39 ]. The initial concentration of the enzyme solution was 0.015 mg/mL in 0.1 M phosphate buffer (pH 6.9) and the initial concentration of the substrate solution was 1 mM in the same phosphate buffer.…”
Section: Methodsmentioning
confidence: 99%