A kind of pyridine-containing compound and its extraction method
An extraction method and compound technology are applied in the field of pyridine-containing compounds and their extraction, and can solve the problems such as no reports of compounds inhibiting COX-2.
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Embodiment 1
[0023] Example 1 Extraction, separation and structural identification of the compound of the present invention
[0024] Japanese Pipa A 50kg, crushed, extracted with 70% ethanol cold soaking for 3 times, each time for 48h, 6 times the volume, stirring continuously, filtering, recovering ethanol under reduced pressure, to obtain 4kg extract, suspending in acid water, adjusting pH 1–2 , extracted 4 times with equal volume of ethyl acetate to obtain 1 kg of non-alkaloid fraction. The pH of the remaining acidic aqueous layer was adjusted to neutral or slightly alkaline with alkali, and extracted 4 times with equal volume of ethyl acetate to obtain 300 g of alkaloid fraction. The alkaloid fraction (300g) was chromatographed on MCI gel CHP 20P column, methanol / water (10:90, 20:80, 30:70, 40:60, 50:50, 60:40, 70:30, 80:20 , 90:10, 100:0) gradient elution, TLC detection and combining the same fractions to obtain Fractions A-E a total of 5 fractions. Fr.D (20 g) was separated by Seph...
Embodiment 2
[0029] Embodiment 2 compound inhibits COX-2 test method
[0030] In this experiment, Cayman’s COX Fluorescent Inhibitor Screening Assay Kit was used to detect the enzymatic activity of COX-2. Specific steps are as follows:
[0031] Compound gradient dilution: Dissolve the compound in DMSO into a 10mM stock solution, and then use DMSO to dilute it 1:3 into a 1000×compound serial concentration stock solution with 10 concentration gradients, and then transfer it to a 384PP plate adapted to the compound transfer instrument for later use.
[0032] Add 10 μl of enzyme diluent to each well, and add 10 μl of 1xassay buffer to blank control wells without adding enzyme.
[0033] The compound was transferred to 20 nl of 1000× gradient diluted compound and added to the reaction solution, and DMSO was added to the blank control and DMSO control wells. Incubate at room temperature for 10-15min.
[0034] Dilute the fluorescent substrate ADHP and coenzyme Heme with 1xassay buffer, the dilu...
Embodiment 3
[0038] The compound in Example 1 can be prepared into an injection solution after adding injection solvent according to the conventional method, finely filtering, filling and sterilizing.
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