BLU-945

本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断

BLU-945 是一种强效、高选择性、可逆的表皮生长因子受体酪氨酸激酶抑制剂 (TKIs)，具有口服活性。BLU-945 可有效抑制具有 L858R 和/或外显子 19 缺失突变、T790M 突变和 C797S 突变的 EGFR。BLU-945 可用于肺癌包括非小细胞肺癌（NSCLC）的研究。

BLU-945 is a potent, highly selective, reversible and orally active epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKIs). BLU-945 can effectively inhibit EGFR with L858R and/or exon 19 deletion mutation, T790M mutation and C797S mutation. BLU-945 can be used for the research of lung cancer including non-small cell lung cancer (NSCLC).

——

Animal Model:triple-mutant osimertinib-resistant Ba/F3 CDX and PDCX models Dosage:0-100 mg/kg Administration:oral, twice daily Result:Showed significant tumor regression in an osimertinib-resistant EGFR ex19del/T790M/C797S PDCX.

——

Angiogenesis

EGFR

EGFR

——

——

2660250-10-0

556.7

C28H37FN6O3S

>98% (HPLC)

In Vitro:?DMSO 中的溶解度 : 100 mg/mL (179.63 mM; 超声助溶 )

CO[C@@H]1CCN(C[C@@H]1F)c1nccc(Nc2cc3c(ccc(N4C[C@H](CS(C)(=O)=O)[C@H]4C)c3cn2)C(C)C)n1

——

(-20℃)

With Ice Pack

≥ 2 years