A kind of prenyl flavone and its application in the preparation of medicine for treating inflammatory diseases
A technology of prenyl flavonoids and inflammatory diseases, which is applied in the field of application of prenyl flavonoids in the preparation of drugs for treating inflammatory diseases, and can solve tissue damage, blockage of microcirculation, damage to vascular endothelial cells and blood vessels Extracellular issues
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Embodiment 1
[0018] Example 1 Preparation of prenyl flavone artoheteroid C in jackfruit
[0019] The jackfruit root medicinal material (17 Kg) was extracted by leakage with 95% ethanol, and the extract was concentrated under reduced pressure to obtain 1.5 Kg of extract. The extract was suspended in water, extracted successively with petroleum ether, chloroform, ethyl acetate and n-butanol, and concentrated to dryness respectively. Take 532 g of the extract from the chloroform extraction part, perform macroporous resin column chromatography (column size: 15*55cm, 5.3 Kg), and elute with ethanol-water gradient to obtain 10 fractions frs. H1-H10. Fraction H5 (10.0 g) was applied to a Sephadex LH-20 column and eluted with methanol to obtain 10 fractions: frs.H5L1-H5L10. Fraction H5L5 (1.5 g) was applied to a reverse ODS column and eluted with methanol-water (2:8→10:0, v / v) to obtain 4 fractions H5L5O1-H5L5O4. Fraction H5L5O4 (483.0 mg) was further applied to Sephadex LH-20 gel column, eluted...
Embodiment 2
[0020] Example 2 Structural Identification of the Prenyl Flavone Artoheteroid C in Jackfruit
[0021] Artoheteroid C, a yellow amorphous powder with quasi-molecular ion peaks by HR-ESI-MS m / z 381.0979 ([M-H] - , C 21 h 17 o 7 , Calculated value: 381.0980), confirm its molecular formula as C 21 h 18 o 7 . IR ( ν max 3430, 2974, 1651, 1612, 1504, 1467, 1356 cm -1 ) and UV spectra ( lambda max 263, 316, 378nm) shows that the compound has typical absorption characteristics of prenylflavonoids. Artoheteroid C's 1 HNMR spectrum (600 MHz, dimethyl sulfoxide- d 6 ) shows the following proton signal: a hydrogen-bonded hydroxyl δ H 12.33 (1H, s, OH-5); a pair of meta-coupled aromatic protons δ H 6.33 (1H, d, J = 1.8 Hz, H-8) and6.13 (1H, d, J = 1.8 Hz, H-6); a lone aromatic proton δ H 6.38 (H-3'); a methoxy group δ H 3.77 (3H, s, MeO-4′); two methyl groups δ H 1.57 (3H, s, H 3 -14) and 1.23 (3H, s, H 3 -15) and an ABX-type spin-coupled system δ H 2...
Embodiment 3
[0025] Example 3 Cytotoxicity evaluation experiment of artoheteroid C on rat PMNs
[0026] The cytotoxicity of artoheteroid C on PMNs was determined by referring to the relevant literature of the standard trypan blue exclusion method. At 37°C, 1 mL of PMNs cell suspension (1×10 6 ) (2% FCS-HBSS) were incubated with 10 μL DMSO or artoheteroid C (final concentration ranging from 1 to 1000 μM) for 30 min. Add 112 μL of 0.4% trypan blue staining solution to each sample, and under a high-power microscope, calculate the cytotoxic effect of the sample on PMNs by counting the absorption of trypan blue by 100 cells. The results showed that artoheteroid C at 180 M above began to show toxicity to PMNs.
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