Application of bis-indole compound FGFC1 in preparation of medicaments resistant to non-small cell lung cancer
A technology for non-small cell lung cancer and bisindole compound, which is applied in the application field of bisindole compound and the preparation of anti-non-small cell lung cancer drugs, and can solve the problems of limiting therapeutic efficacy and the like
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Embodiment 1
[0030] Inhibitory effect of FGFC1 on proliferation of cell lines of different tumor types.
[0031] (1) Cell inoculation: Four tumor cell lines (HCT116, HeLa, PC9 and MCF7) in the exponential growth phase were digested respectively, and suspensions were prepared with RPMI1640 or DMEM medium containing 10% calf serum. Tumor cells were seeded at 1×10 5 cells / mL inoculated in 96-well culture plate, add 100 μL to each well, at 37°C, CO 2 Cultivate in the incubator for 24h.
[0032] (2) Dosing: the compound to be tested was prepared into a stock solution with a certain concentration by adding DMSO, and then prepared into 5 μmol / L and 50 μmol / L solutions with RMPI1640 or DMEM medium containing 10% calf serum, and inoculated in 96 In a well-plated cell culture plate, set up three parallel wells for each concentration, at 37°C, 5% CO 2 Cultivate in the incubator for 48h. The control group was treated with DMSO, without adding drugs, and continued to culture for 48 hours. The chang...
Embodiment 2
[0036] The results of morphological changes of non-small cell lung cancer lines containing different driver genes treated with different concentrations of FGFC1 for the same time.
[0037] (1) Inoculated cells: respectively digest non-small cell lung cancer cell lines in exponential growth phase containing different driver genes: EGFR sensitive mutation PC9 (ex19del), EGFR primary resistance mutation H1975 (L858R / T790M), EGFR wild type A549 (KRAS mutation), H1299 (NRAS mutation). Suspension was made with RPMI1640 or DMEM medium containing 10% calf serum. The tumor cells were seeded with a cell number of 0.5×10 5 cells / mL inoculated in 12-well culture plate, add 2 mL to each well, at 37°C, CO 2 Cultivate in the incubator for 24h.
[0038] (2) Dosing: the compound to be tested was prepared into a stock solution with a certain concentration by adding DMSO, and then prepared into 5 μmol / L and 50 μmol / L solutions with RMPI1640 or DMEM medium containing 10% calf serum, and inoculat...
Embodiment 3
[0041] Inhibitory effect of FGFC1 on non-small cell lung cancer cell lines harboring different driver genes.
[0042] (1) Inoculated cells: respectively digest non-small cell lung cancer cell lines in exponential growth phase containing different driver genes: EGFR sensitive mutation PC9 (ex19del), EGFR primary resistance mutation H1975 (L858R / T790M), EGFR wild type A549 (KRAS mutation), H1299 (NRAS mutation). Suspension was made with RPMI1640 or DMEM medium containing 10% calf serum. Tumor cells were seeded at 1×10 5 cells / mL inoculated in 96-well culture plate, add 100 μL to each well, at 37°C, CO 2 Cultivate in the incubator for 24h.
[0043] (2) Dosing: the compound to be tested was prepared into a stock solution with a certain concentration by adding DMSO, and then prepared into 0.01, 0.1, 1, 2, 5, 10, 20 respectively with RMPI1640 or DMEM medium containing 10% calf serum , 40, 80, and 100 μmol / L solutions, inoculated in 96-well cell culture plates, and set up three p...
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