A kind of lignan compound in purslane and its extraction and separation method and application
A technology of lignans and separation methods, which is applied in the field of extraction and separation of lignans, can solve the problems of low structural novelty, and achieve the effects of environmentally friendly process methods, simple and fast operation methods
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Embodiment 1
[0036] Example 1 Extraction and separation of lignans from purslane and its extraction and separation method.
[0037] A kind of lignan compound extracted and separated from purslane, the molecular formula of this compound is C 20 h 18 o 6 , and named olealignan A, its chemical structure is as follows:
[0038] ,
[0039] Described compound is called olealignan A, and table 1 is the NMR data of this new compound: 1 H-NMR with 13 C-NMR in deuterated DMSO.
[0040] Table 1. NMR data of the new compounds of the present invention.
[0041] .
[0042] The structural identification of a kind of lignan compound extracted and separated from purslane refers to Figure 1-10 , the biological structure identification and deduction of the compound are as follows.
[0043] Oleralignan A: yellow powder, easily soluble in methanol. HR-ESI – - MS gives m / z 353.1021 [M-H] – The quasi-molecular ion peak has a molecular weight of 353.1031. combine 1 H-NMR, 13 According to C-NMR...
Embodiment 2
[0053] Example 2 Antitumor effect of the new compound of the present invention.
[0054] 1 main material.
[0055] 1.1 Drugs and reagents.
[0056] The new compound used in the experiment was prepared by the above method with a purity of 90-99%, weighed accurately, and diluted with DMSO to the solution required for each dosage group below. DMEM high glucose medium, fetal bovine serum (Hyclone Company, USA); penicillin, streptomycin (Hangzhou Sijiqing Company).
[0057] 1.2 Cell lines.
[0058] Human colon cancer cell Caco-2, human breast cancer cell MCF-7, human gastric cancer cell BGC-823, human lung adenocarcinoma cell SPC-A1, human liver cancer cell BEL-7402, human cervical cancer cell Hela-229, ovarian cancer cell Ho-8910, human oral epidermoid carcinoma cells KB (Shanghai Cell Bank, Chinese Academy of Sciences).
[0059] 1.3 Grouping.
[0060] Divided into control group, experimental group and zero adjustment group (culture solution containing DMSO vehicle).
[0061...
Embodiment 3
[0070] Example 3 Anticholinesterase effect of compounds of the present invention.
[0071] 1 main material.
[0072] 1.1 Drugs and reagents.
[0073] The lignan compounds used in the experiment were prepared by the above method with a purity of 90-99%. Sodium dihydrogen phosphate, disodium hydrogen phosphate (Sinopharm Chemical Reagent Co., Ltd.), physostigmine (Hanxiang Biotechnology), 5,5' -Dithiobisnitrobenzoic acid (DTNB, Shanghai Jinsui Biotechnology Co., Ltd.), acetylcholinesterase (AChE) and acetylthiocholine iodide (ATCI, Dalian Meilun Biological Co., Ltd. Technology Co., Ltd).
[0074] 1.2 Grouping.
[0075] Divided into negative control group, positive control group and experimental group, each group.
[0076] 2. Experimental method.
[0077] 2.1 Sample preparation.
[0078] Precisely weigh the sample and 1 mg of physostigmine, respectively, and use methanol as the solvent to prepare five gradient concentrations of (5, 10, 20, 30, 50 μM / mL). Accurately weigh 7...
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