A kind of ester compound in purslane and its extraction and separation method and application
The technology of an ester compound and a separation method is applied to an ester compound in purslane and the field of extraction and separation thereof, which can solve the problems of low structural novelty and the like, and achieves environmental protection of the process method, significant anticholinesterase activity, Simple operation and quick results
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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] .
[0041] The compound is light yellow oil, easily soluble in methanol, insoluble in water. HRESI(+)TOFMS gives m / z: 323.2584[M+H] + The quasi-molecular ion peak has a molecular weight of 323.2586. combine 1 H-NMR, 13 According to C-NMR and DEPT data, it is speculated that the possible molecular formula of the compound is C 20 h 34 o 3 , with an unsaturation of 4. 13 C-NMR spectrum and DEPT spectrum show 20 carbon signals, respectively 2 CH3 (δ: 13.82; 14.10), 12 C...
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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