Glechoma longituba phenol, and preparation method and application thereof
A technology of fenugreek and medicinal plants, which is applied in the field of fenugreek and its preparation, can solve the problem that a certain compound or several compounds with no specific anticoagulation and thrombolytic effects are given, and the variety of compounds can be enriched. , good anti-oxidation, wide range of effects
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Embodiment 1
[0056]The extraction separation of embodiment 1 compound I, II, III
[0057] (1) Extraction and separation
[0058] 1) Take 16.0kg of the dried whole herb of the medicinal plant Styracis chinensis, and ultrasonically extract it twice with distilled water, each time for 30 minutes. Then the filter residue was reflux extracted with water for 1 h, all the extracts were combined, and concentrated by rotary evaporation to obtain the extract;
[0059] 2) Suspend the extract with distilled water, and then repeatedly extract with ethyl acetate and n-butanol, respectively, to obtain the ethyl acetate extraction part and n-butanol extraction part, which are concentrated under reduced pressure and dried to obtain the ethyl acetate extraction part respectively. extracts and n-butanol extracts;
[0060] 3) The ethyl acetate extract was subjected to silica gel column chromatography, and gradient elution was carried out with ethyl acetate and methanol (the volume ratio of ethyl acetate to ...
Embodiment 2
[0087] The antioxidant activity of embodiment 2 compound I, II, III
[0088] (1) Experimental samples: cyclamol A, cyclamol B, cyclamol C;
[0089] (2) Experimental instruments and reagents: constant temperature shaking incubator, microplate reader, Vc, 1,1-diphenyl-2-trinitrophenylhydrazine (DPPH), Milli-Q water;
[0090] (3) Experimental method: DPPH method was used to measure the antioxidant activity of Dichryonol A-C, and Vc was used as a positive drug to investigate the established model.
[0091] Dissolve Limobilol A-C in DMSO, and dilute with Milli-Q water to a gradient concentration of 50 μmol / L, 25 μmol / L, 12.5 μmol / L, 6.25 μmol / L, 3.125 μmol / L, and 1 μmol / L. Set the test group, background group, and control group, among which,
[0092] Test group: sample 100μL+DPPH100μL;
[0093] Blank group: 100 μL of sample + 100 μL of ethanol;
[0094] Control group: water 100μL+DPPH100μL;
[0095] After mixing, shake and incubate at 37°C for 1 h, measure the OD value at 517 ...
Embodiment 3
[0099] Example 3 Compound I, II, III to H 2 o 2 Protection from H9c2 Cardiomyocyte Injury
[0100] (1) Experimental samples: cyclamol A, cyclamol B, cyclamol C;
[0101] (2) Experimental equipment and reagents: H9c2 cardiomyocytes, thiazolium blue (MTT), DMEM high-glucose medium, fetal bovine serum, double antibodies, DMSO, CO 2 Incubator, inverted microscope, ultra-clean bench, plate shaker;
[0102] (3) Experimental method: Count H9c2 cardiomyocytes and culture them in 96-well flat-bottom culture plates; Respectively pre-protected, and then cultured in a cell culture incubator for 12h; then with 450μmol / L H 2 o 2Treat for 4 hours to create a model of cell oxidative damage, and use the MTT method to measure cell viability to observe the effect of the sample on H 2 o 2 Protection against oxidative damage in cardiomyocytes. Test results such as Figure 23 As shown, the Control group in the figure represents the survival rate of cardiomyocytes without hydrogen peroxide ...
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