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CH7233163

目录号 : GC25219

CH7233163 is a non-covalent ATP competitive inhibitor of EGFR-tyrosine kinase with antitumor activities against tumor with EGFR-Del19/T790M/C797S.

CH7233163 Chemical Structure

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5mg
¥3,663.00
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25mg
¥15,307.00
现货

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Sample solution is provided at 25 µL, 10mM.

Description

CH7233163 is a non-covalent ATP competitive inhibitor of EGFR-tyrosine kinase with antitumor activities against tumor with EGFR-Del19/T790M/C797S.

CH7233163 shows potent antitumor activities against tumor with EGFR-Del19/T790M/C797S in vitro. CH7233163 potently inhibits the proliferation of Del19/T790M/C797S_NIH3T3 cells with IC50 of 20 nmol/L. CH7233163 potently and dose-dependently blocks the EGFR phosphorylation in the Del19/T790M/C797S_NIH3T3 cells. CH7233163 can inhibit Del19/T790M/C797S signaling.[1]

Pharmacodynamic study is performed using Del19/T790M/C797S_NIH3T3 xenografted tumors in mice. CH7233163 clearly inhibits EGFR phosphorylation after oral administration and potent tumor regression is observed. CH7233163 has potent therapeutic efficacy against tumors with EGFR-Del19/T790M/C797S in vivo.[1]

[1] Kenji Kashima, et al. Mol Cancer Ther. 2020 Sep 17;molcanther.0229.2020.

化学性质

Cas No. unknown SDF Download SDF
分子式 C31H34F3N9O3S 分子量 669.72
溶解度 DMSO: 100 mg/mL (149.32 mM);Water: Insoluble;Ethanol: Insoluble 储存条件 Store at -20°C
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1 mg 5 mg 10 mg
1 mM 1.4932 mL 7.4658 mL 14.9316 mL
5 mM 0.2986 mL 1.4932 mL 2.9863 mL
10 mM 0.1493 mL 0.7466 mL 1.4932 mL
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