Tertiary amide tubulin polymerization inhibitor and its preparation method and application
A technology of polymerization inhibitor and tubulin, which is applied in the field of anti-tumor medicinal chemistry, can solve the problems of high toxicity and achieve the effect of high yield and simple and efficient synthesis method
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Embodiment 1
[0018] The preparation of embodiment 1 general formula (II)
[0019] (1) The preparation method of compound (I):
[0020] In an ethanol solvent, at a temperature of 60-120°C, the aryl-substituted methylene chloride compound and different substituted anilines were stirred and reacted under a bar of sodium hydroxide to obtain compound I.
[0021] (2) The preparation method of compound (II):
[0022] Compound (I) (5 mmol) and different substituted acetyl chloride compounds (5 mmol) were added into 15 mL of acetone to dissolve, and the reaction was stirred at 80 degrees Celsius. TLC monitors the reaction process. After the reaction is over, add distilled water to the system, then extract 3 times with dichloroethane, then back-extract the dichloroethane phase with saturated brine for 2 times, each 20mL, and finally the organic phase is extracted with dichloroethane. Dry over magnesium sulfate, filter out the magnesium sulfate, and distill the filtrate under reduced pressure to re...
Embodiment 2
[0059] The antitumor activity determination of the above-mentioned compound of embodiment 2:
[0060] The compounds used in the screening are all synthesized and purified by the present invention; sample stock solution: weigh 1-2mg of the sample and place it in a 2mL EP tube, then make a solution with DMSO, store it at 4°C, and use the culture medium according to the required concentration during the experiment. base dilution. Take the cells in the logarithmic growth phase, digest and count them, adjust the cell density with the medium, inoculate 4000-5000 cells / well into a 96-well plate, 150 μL per well, cultivate for 24 hours, discard the medium, and add the culture medium Base-diluted drugs (50 μg / mL, 100 μg / mL), 6 replicate wells were set up for each concentration, and a blank control group and a negative control group were also set up. After 72 hours of drug action, add 20 μL MTT to each hole, continue to cultivate for 4 hours, absorb the liquid, add 150 mL of DMSO, shak...
Embodiment 3
[0066] The determination of the Tubulin polymerization inhibitory activity of embodiment 3 compound IId:
[0067] The extracted tubulin was resuspended in ice-cold G-PEM buffer (80mM PIPES pH 5.9, 5mM MgCl 2 , 1mM EGTA, 1mM ATP, 5% (v / v) glycerol), take 100ul and add it to a 96-well plate containing 100ul compound IId, the final concentration of tubulin is 5.6g / L, and the drug concentration is set to 0uM, 1uM, 2uM , four gradients of 4uM, the sample was fully mixed, the aggregation of tubulin was detected by spectrophotometer, the interval was 5min, the total was 60min, IC 50 Values were calculated at 30 minutes using GraphPad software. Conclusion: The enzymatic activity of compound IId on microtubules is less than 3uM.
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