Preparation method and application of a kind of triterpene compound in walnut green husk
A technology of walnut green skin and compound, applied in the field of medicine, can solve problems such as pollution of the environment
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Embodiment 1
[0028] The preparation method of Qinglongyi triterpene macrocyclic ketal I:
[0029] (1) Alcohol extraction: 5 kg of dried walnut green skin was properly crushed, and then 50 L of 95% ethanol was added for reflux extraction, each time for 2 hours, and a total of 3 extractions. The extracts were combined, and the extracts were reclaimed under reduced pressure to obtain 526g of ethanol crude extract extract;
[0030] (2) Enrichment and purification of macroporous resin: disperse the crude ethanol extract obtained in step (1) with water to a solution with a relative density of 1.20±0.05g / mL, enrich and purify by AB-8 macroporous resin column chromatography (The inner diameter of the chromatographic column is 8cm, the length is 1.50m, and the effective height of the resin is 1.05m), and eluted with 30% ethanol and 90% ethanol in sequence, and the 90% ethanol eluate is collected, and the solvent is recovered under reduced pressure to obtain the 90% ethanol eluted part Extract 98.5...
Embodiment 2
[0036] Compound Identification:
[0037] The compound of the present invention prepared in Example 1 is a white amorphous powder (MeOH). Positive HR-ESI-MS spectra, such as figure 2 shown in m / z Visible at 536.9833 [M+K] + The ion peak indicates that the molecular weight of the compound is 498. to combine 1 H-NMR, 13 C-NMR and DEPT spectra speculate that its molecular formula is C 33 h 54 o 3 , calculating its degree of unsaturation to be 11.
[0038] Compounds of the present invention 1 H-NMR (CDCl 3 , 400 MHz) spectrum, there are seven unimodal methyl proton signals in the high field region, which are assigned as follows: δ 1.68, 1.29, 0.98, 0.94, 0.93, 0.89, 0.84 (3H×7, s , CH 3 -33,CH 3 -21,CH 3 -18,CH 3 -28,CH 3 -30,CH 3 -19, CH 3 -29), which is the hydrogen spectrum data of typical dammarane-type triterpenes. In addition, there are also δ 5.55 (1H, dd , J = 6.1 Hz), δ 3.80 (1H, td , J = 5.7,10.8 Hz) and δ 3.40(1H, t , J = 2.8 Hz) th...
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