Lignan compound in herba portulacae and extraction and separation method and application of lignan compound
A technology of lignans and separation method, which is applied in the field of extraction and separation of lignans, can solve the problems of low structural novelty and the like, and achieves the effects of environmental protection of the process method, simple and fast operation method
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Embodiment 1
[0036] Example 1 Extracting and separating 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. to combine 1 H-NMR, 13 According to C-NMR and...
Embodiment 2
[0053] Example 2 Anti-tumor 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-mentioned method with a purity of 90-99%. It was accurately weighed and diluted with DMSO to the solution required for each dosage group below. DMEM high-glucose medium, fetal bovine serum (Hyclone Company of the United States); penicillin and 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 solutio...
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 compound used in the experiment was 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 a solvent to prepare five gradient concentrations of (5, 10, 20, 30, 50 μM / mL). Accurately weigh 7.09...
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