Three kinds of alkaloid compounds in purslane and their extraction and separation methods
A technology of alkaloids and separation methods, applied in the field of three alkaloid compounds and their extraction and separation, can solve the problem of low structural novelty, and achieve the effect of environmentally friendly process methods, simple and fast operation methods
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Embodiment 1
[0059] The present invention provides three kinds of alkaloid compounds, molecular formula is C 16 h 15 NO 5 (1), C 13 h 11 NO 3 (2), C 14 h 13 NO 3 (3), and named according to its structure 4,9,10-trihydroxy-2-methoxy-6,7-dihydrodibenzo[b,e]azocin-12(5H)-one(1), 9,10-dihydroxy- 5,6-dihydro-11H-benzo[d]pyrrolo[1,2-a]azepin-11-one (2), 8,9-dihydroxy-6,11-dihydro-5H-benzo[d]pyrrolo[1 ,2-a]azepine-3-carbaldehyde (3), the chemical structural formula is:
[0060] .
[0061] The NMR data of the three alkaloid compounds are shown in Table 1: 1 H-NMR with 13 C-NMR in MeOD.
[0062] Table 1: NMR data of three alkaloid compounds of the present invention
[0063] .
[0064] The alkaloid compound 1 of the present invention is named 4,9,10-trihydroxy-2-methoxy-6,7-dihydrodibenzo[b,e]azocin-12(5H)-one according to its structure identification and derivation, Table 1 is NMR data of the alkaloid compound.
[0065] 4,9,10-trihydroxy-2-methoxy-6,7-dihydrodibenzo[b,e]azocin-1...
Embodiment 2
[0079] Example 2 Anti-inflammatory effects of three alkaloid compounds of the present invention.
[0080] 1. Main materials.
[0081] 1.1. Drugs and reagents: The compounds used in the experiment were prepared by the above method with a purity of ≥98%, weighed accurately, and diluted with DMSO to the required solutions for the following dosage groups. Fetal bovine serum (U.S. Hyclone Company); penicillin and streptomycin (Hangzhou Sijiqing Company); DMSO (U.S. Sigma Company); CCK-8 kit (Wuhan Boster Bioengineering Co., Ltd.); DMEM high glucose medium, LPS , IL-1 β , TNF- α ELISA kit (Soleibao Technology Co., Ltd.); cell lysate.
[0082] 1.2 Cell line: RAW264.7 macrophages (US ATCC cell bank).
[0083] 1.3 Grouping: control group, LPS group and experimental group, each group.
[0084] 2 Experimental methods.
[0085] 2.1 Cell culture, DMEM high-glucose medium, add 10% fetal bovine serum, 1% antibiotics (100U / mL penicillin and 100μg / mL streptomycin), place at 37°C, 5% CO ...
Embodiment 3
[0098] Example 3 Anticholinesterase effect of three compounds of the present invention.
[0099] 1. Main materials.
[0100] Drugs and reagents: The alkaloid compounds used in the experiment were prepared by the above method with a purity of ≥98%, 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 iodide thioacetylcholine (Acetylthiocholine iodide, ATCI, Dalian Meilun Biotechnology Co., Ltd.).
[0101] 2. Grouping: divided into blank group, control group and sample group.
[0102] 3 Experimental methods.
[0103] 3.1 Sample preparation
[0104] Precisely weigh the sample and 0.11 mg of physostigmine, respectively, and use methanol as a solvent to prepare five gradient concentrations of 2.5 μM, 5.0 μM, 10.0 μM, 20.0 μM and 40.0 μM. Accur...
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