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首页-小分子抑制剂&激动剂-Tyrosine Kinase-EGFR-BI-1622
BI-1622

Chemical Structure : BI-1622

CAS No.: 2681392-19-6

BI-1622 (BI 1622)

货号: PC-49227Not For Human Use, Lab Use Only.

BI-1622 (BI 1622) is a potent, selective, covalent and orally active HER2 inhibitor with IC50 of 7 nM, potently inhibits HER2 exon 20 mutants while sparing WT EGFR.

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10 mg ¥4280 In stock
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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

BI-1622 (BI 1622) is a potent, selective, covalent and orally active HER2 inhibitor with IC50 of 7 nM, potently inhibits HER2 exon 20 mutants while sparing WT EGFR.
BI-1622 (5 uM) inhibits the proliferation of HER2-dependent cell lines, dose-dependently decreases pHER2 and pERK levels in NCI-H2170 HER2YVMA and PC-9 HER2YVMA cells.
BI-1622 inhibits tumor growth and inhibits oncogenic signaling in preclinical xenograft models of HER2 exon 20 mutant non-small cell lung cancer.

物理化学性质&存储条件

分子量 508.54
分子式 C26H24N10O2
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

2-Propen-1-one, 1-[4-[8-[[3-methyl-4-([1,2,4]triazolo[1,5-a]pyridin-7-yloxy)phenyl]amino]pyrimido[5,4-d]pyrimidin-2-yl]-1-piperazinyl]-

参考文献

1. To C, et al. Nat Cancer. 2022 Apr;3(4):402-417.

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