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Tuxobertinib

CAS No. : 2414572-47-5

MCE 国际站：Tuxobertinib

产品活性：Tuxobertinib (BDTX-189) 是一种高效的具有口服活性的选择性 EGFR、HER2 变构突变抑制剂，包括 EGFR/HER2 外显子 20 插入突变。Tuxobertinib 对 EGFR、HER2、BLK 和 RIPK2 的K_D 值分别显示 0.2、0.76、13 和 1.2 nM。具有抗癌活性。

研究领域：JAK/STAT Signaling  |  Protein Tyrosine Kinase/RTK

作用靶点：EGFR

In Vitro: Tuxobertinib is a masterKey inhibitor of the ERBB allosteric mutant oncogene family with antiproliferative activity (IC₅₀<100 nM for ERBB allosteric mutant oncogene family).

In Vivo: Tuxobertinib (0-100 mg/kg; p.o.; daily for 15 dyas) shows dose-dependent tumor growth inhibition and regression in in athymic nude mice bearing HER2 S310F Ba/F3 allograft tumors.
Tuxobertinib (1-50 mg/kg.p.o.; daily for 15 days) shows dose-dependent tumor growth inhibition and regression in athymic nude mice bearing CUTO-14 PDX tumors that express the EGFR mutation EGFR ASV.

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