Novel pterocarpan type flavonoid and applications
A technology of flavonoids and pterostane, which is applied in the field of medicine, can solve the problems of few research reports on yuqian, and achieve the effects of simple and fast preparation method, high yield and simple process
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Embodiment 1
[0027] The preparation method of embodiment 1 pterostane type flavonoids
[0028] (1), cut or pulverize the dry elm money (12.0 kg) into small pieces (0.5 cm), soak it with 88% ethanol for 10 hours at room temperature, then carry out heat reflux extraction for 3 times, each time for 3 hours, and filter , the combined filtrates were dried at 48°C under vacuum until there was no alcohol smell, to obtain the total extract of Yuqian (0.95 kg);
[0029] (2), uniformly suspending the total extract of Ulmus chinensis in distilled water (total extract of Ulmus chinensis: distilled water=1:2, V / V), let it stand for 19 hours, and filter to obtain the supernatant;
[0030] (3), the supernatant is extracted successively with sherwood oil, ethyl acetate, n-butanol, and each extract is concentrated under reduced pressure to obtain sherwood oil extract (92.5 grams), ethyl acetate extract (350.0 grams), n-butanol Butanol extract (406.8 grams); 3 kinds of thick extracts carry out α-glucosidas...
Embodiment 2
[0041] The α-glucosidase inhibitory activity assay of embodiment 2 compound I
[0042] (1) Experimental method
[0043] According to the method of Pierre et al. [1-2] , using p-nitrophenyl-β-D-glucopyranoside (PNPG) as the substrate to measure the activity of α-glucosidase.
[0044] Add 10 μL of α-glucosidase with a concentration of 1 U / mL (prepared in 0.1mol / L pH=6.8 phosphate buffer, the same below) to 100 μL buffer (0.1mol / L pH=6.8 phosphate buffer, the same below), at 37 Incubate at ℃ for 10 min, then add 90 μL p-nitrophenyl-β-D-glucopyranoside (PNPG) at a concentration of 0.01 mol / L, incubate at 37 °C for 10 min, and measure the absorbance at a wavelength of 405 nm with a microplate reader (A 酶 ).
[0045] Compound I was dissolved in DMSO to make a mass concentration of 0.625 g / L. Add 10 μL of α-glucosidase at a concentration of 1 U / mL to the sample, add 50 μL of buffer solution and incubate at 37°C for 10 minutes, then add 90 μL of 0.01mol / LPNPG at a concentration of...
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