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首页-小分子抑制剂&激动剂-Tyrosine Kinase-Bcr-Abl-Radotinib
Radotinib

Chemical Structure : Radotinib

CAS No.: 926037-48-1

Radotinib (IY5511, IY-5511)

货号: PC-38025Not For Human Use, Lab Use Only.

Radotinib (IY-5511) is a potent and selective BCR-ABL1 tyrosine kinase inhibitor with IC50 of 34 nM for wild-type BCR-ABL1 kinase.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

Radotinib (IY-5511) is a potent and selective BCR-ABL1 tyrosine kinase inhibitor with IC50 of 34 nM for wild-type BCR-ABL1 kinase.
Radotinib (IY-5511) displays high selectivity over c-kit (1,324 nM), PDGFR (PDGFRα, 75.5 nM; PDGFRβ, 130 nM) and src (>2,000 nM).
Radotinib (IY-5511) effectively inhibited the proliferation of common mutant clones of BCR-ABL1, with the exception of T315I.

物理化学性质&存储条件

分子量 530.5
分子式 C27H21F3N8O
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

4-methyl-N-(3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)-3-((4-(pyrazin-2-yl)pyrimidin-2-yl)amino)benzamide

参考文献

1. Kim SH, et al. Haematologica. 2014 Jul;99(7):1191-6.

2. Heo SK, et al. PLoS One. 2015 Jun 12;10(6):e0129853.

3. Kwak JY, et al. Clin Cancer Res. 2017 Dec 1;23(23):7180-7188.

4. Heo SK, et al. Sci Rep. 2017 Nov 10;7(1):15278.

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