Ester compound in purslane as well as extraction and separation method and application thereof
An ester compound and separation method technology, applied in the field of an ester compound in purslane and its extraction and separation, can solve the problem of low structural novelty, achieve environmental protection of the process method, significant anti-tumor and anti-choline ester Enzyme activity, simple operation method and rapid effect
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Embodiment 1
[0035] Embodiment 1 extracts and separates the ester compound and its extraction and separation method from purslane.
[0036] A kind of ester compound extracted from purslane, molecular formula is C 20 h 34 o 3 , named (7E, 9E)-6-oxoctadecyl-7,9-dienoic acid ethyl ester, the chemical structural formula is:
[0037]
[0038] Table 1 is the nuclear magnetic data of this new compound: 1 H-NMR with 13 C-NMR in DMSO.
[0039] Table 1. NMR data of the new compounds of the present invention.
[0040] serial number δ C
Types of δ H (J in Hz)
1 172.50 C=O 2 33.45 CH 2
2.25,t(7.02) 3 23.53 CH 2
1.48,m 4 23.53 CH 2
1.48,mr 5 39.24 CH 2
2.54,t(7.50) 6 200.10 C=O 7 128.05 CH 6.10,d(15.54) 8 142.74 CH 7.18,m 9 128.96 CH 6.26,m 10 145.37 CH 6.26,m 11 32.38 CH 2
2.17,m 12 24.40 CH 2
1.48,m 13 24.56 CH 2
1.48,m 14 28.42 CH ...
Embodiment 2
[0050] Example 2 Anti-tumor effect of the new ester compound of the present invention.
[0051] 1 main material.
[0052] 1.1 Drugs and reagents.
[0053] The new ester compounds used in the experiment were prepared by the above method with a purity of 90% to 99%. They were accurately weighed and diluted with DMSO to the required solutions for the following dosage groups. DMEM high-glucose medium, fetal bovine serum (Hyclone Company of the United States); penicillin and streptomycin (Hangzhou Sijiqing Company).
[0054] 1.2 Cell lines.
[0055] 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).
[0056] 1.3 Grouping.
[0057] Divided into control group, experimental group and zero adjustment group ...
Embodiment 3
[0067] Example 3 The anticholinesterase effect of the new compound of the present invention.
[0068] 1. Main materials.
[0069] 1.1 Drugs and reagents.
[0070] The new 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), phosphorus 5,5'- Dithiobisnitrobenzoic acid (Dithiobisnitrobenzoic acid, DTNB, Shanghai Jinsui Biotechnology Co., Ltd.), acetylcholinesterase (AChE) and acetylthiocholine iodide (ATCI, Dalian Meilun Biotechnology Co., Ltd. Ltd.).
[0071] 1.2 Grouping.
[0072] Divided into negative control group, positive control group and experimental group, each group.
[0073] 2 Experimental methods.
[0074] 2.1 Sample preparation.
[0075] Precisely weigh the sample and 0.11 mg of physostigmine, respectively, and use methanol as the solvent to prepare five gradient concentrations of 2.5, 5.0...
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