XL-184 (Cabozantinib,BMS907351)

产品编号: DC1097 Featured
XL-184 (Cabozantinib,BMS907351)
结构式
849217-68-1
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中国地区超过5000个高品质化合物库存
应用领域
Cabozantinib是一种有效的多受体酪氨酸激酶抑制剂, 抑制VEGFR2,c-Met,Kit,Axl 和 Flt3 的 IC50 分别为0.035,1.3,4.6,7 和 11.3 nM。
Cas No.: 849217-68-1
名称: N-(4-(6,7-dimethoxyquinolin-4-yloxy)phenyl)-N-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide
别名: XL184, Cabozantinib, BMS907351, BMS-907351, BMS 907351
SMILES: COC1=CC2=C(C=CN=C2C=C1OC)OC3=CC=C(C=C3)NC(=O)C4(CC4)C(=O)NC5=CC=C(C=C5)F
分子式: C28H24FN3O5
分子量: 501.51
纯度:
保存条件: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description:
In Vivo:
In Vitro:
References: Description of Cabozantinib: Cabozantinib (XL 184) is an orally bioavailable, small molecule receptor tyrosine kinase (RTK) inhibitor with potential antineoplastic activity. Cabozantinib strongly binds to and inhibits several tyrosine receptor kinases. Specifically, cabozantinib appears to have a strong affinity For the hepatocyte growth factor receptor (Met) and vascular endothelial growth factor receptor 2 (VEGFR2), which may result in inhibition of tumor growth and angiogenesis, and tumor regression. This agent has also been shown to inhibit mast/stem cell growth factor (KIT), FMS-like tyrosine kinase 3 (Flt3) and tyrosine-protein kinase receptor (Tie-2). Check For active clinical trials or closed clinical trials using this agent. (NCI Thesaurus). For the detailed information about the solubility of XL-184 (Cabozantinib, BMS907351) in water, the solubility of XL-184 (Cabozantinib, BMS907351) in DMSO, the solubility of XL-184 (Cabozantinib, BMS907351) in PBS buffer, the animal experiment(test) of XL-184 (Cabozantinib, BMS907351), the in vivo,in vitro and clinical trial test of XL-184 (Cabozantinib, BMS907351), the cell experiment(test) of XL-184 (Cabozantinib, BMS907351), the IC50, EC50 and Affinity of XL-184 (Cabozantinib, BMS907351) , please contact DC Chemicals.
Kinase Assay:
Cell Assay:
Animal Administration:
References:
MSDS
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COA
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