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首页-小分子抑制剂&激动剂-Tyrosine Kinase-IGF-1R-Linsitinib
Linsitinib

Chemical Structure : Linsitinib

CAS No.: 867160-71-2

Linsitinib (ASP-7487;ASP 7487;OSI-906;OSI906)

货号: PC-42436Not For Human Use, Lab Use Only.

Linsitinib (ASP-7487, OSI-906) is a potent, selective, orally active, dual IGF-1R/insulin receptor inhibitor with IC50 of 35/75 nM, respectively.

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

生物&药学活性

Linsitinib (ASP-7487, OSI-906) is a potent, selective, orally active, dual IGF-1R/insulin receptor inhibitor with IC50 of 35/75 nM, respectively.
Linsitinib (ASP-7487, OSI-906) potently and selectively inhibits autophosphorylation of both human IGF-1R and IR, displays in vitro antiproliferative effects in a variety of tumor cell lines.
Linsitinib (ASP-7487, OSI-906) shows robust in vivo anti-tumor efficacy in an IGF-1R-driven xenograft model.

物理化学性质&存储条件

分子量 421.4937
分子式 C26H23N5O
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

Cyclobutanol, 3-[8-amino-1-(2-phenyl-7-quinolinyl)imidazo[1,5-a]pyrazin-3-yl]-1-methyl-, cis-

参考文献

1. Mulvihill MJ, et al. Future Med Chem. 2009 Sep;1(6):1153-71.

2. Pitts TM, et al. Clin Cancer Res. 2010 Jun 15;16(12):3193-204.

3. Buck E, et al. Mol Cancer Ther. 2010 Oct;9(10):2652-64.

4. Kuhn DJ, et al. Blood. 2012 Oct 18;120(16):3260-70.

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