A pyrazolo[5,6-d]pyrimidine EGFR inhibitor and its antitumor activity
A tumor and tumor-related technology, applied in anti-tumor drugs, organic active ingredients, medical preparations containing active ingredients, etc., can solve the problems of unclear structure-activity relationship of EGFR inhibitors and great differences in EGFR inhibitory effects.
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Embodiment 1
[0020] The activity and selectivity of the compounds of Example 1 inhibiting EGFR in vitro
[0021] Screening of EGFR kinase in vitro activity: The method used in the experiment is Caliper Mobility Shift Assay, which is a detection platform based on the mobility detection technology of microfluidic chip technology. Experimental steps: configure 1.25x kinase reaction buffer (62.5mmol / L HEPES, pH 7.5; 0.001875% Brij-35; 12.5mmol / LMgCl2; 2.5mM DTT) and kinase reaction termination solution (100mmol / L HEPES, pH 7.5; 0.015 %Brij-35; 0.2% Coating Reagent#3); Add 10 μl of 2.5x FGFR1 Kinase Solution (in 1.25x Kinase Reaction Buffer) Add kinase), incubate at room temperature for 10min, then add 10μl of 2.5x substrate peptide solution (add FAM-labeled peptide and ATP to 1.25x kinase reaction buffer), add 25μl kinase reaction stop solution after reacting at 28°C for a specific time . Test and collect data on Caliper, inhibition rate of kinase activity=(max-conversion) / (max-min)*100. "m...
Embodiment 2
[0024] Antitumor activity verification of compound on the cell level in Example 2
[0025] The anti-tumor activity of compound WZ00411 at the cell level by MTT method was selected to contain EGFR T790M Highly expressed human NSCLC cell line (H1975), EGFR WT Seven kinds of cells, including the highly expressed human large cell lung cancer cell line (A549) and the human lung cancer cell line with primary dislocation mutation of EGFR (HCC827), were tested for their proliferation inhibitory activity. During the determination, PBS was used as the blank control, EGF was used as the negative control, (EGF+WZ4002) was used as the positive control, (EGF+sample to be tested) was used as the experimental group, 6 concentration gradients were set for each sample, and the IC was calculated. 50 value.
[0026] The effect of active compounds on intracellular EGFR pro-proliferation signaling pathway: the compound WZ00411 was selected, and EGF combined with different concentrations of WZ0041...
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