| 名称 | Linifanib |
| 描述 | Linifanib (AL-39324) (ABT-869) is a novel, potent ATP-competitive VEGFR/PDGFR inhibitor for KDR (IC50: 4 nM), CSF-1R (IC50: 3 nM), Flt-1/3 (IC50: 3/4 nM) and PDGFRβ (IC50: 66 nM). Linifanib may exhibit potent antiproliferative and apoptotic effects on tumor cells whose proliferation is dependent on mutant kinases, such as FMS-related tyrosine kinase receptor-3 (FLT3). |
| 细胞实验 | Cells are seeded into 96-well plates at 2.5 × 103 per well and incubated with serum-free medium for 24 hours. Linifanib and VEGF (final, 10 ng/mL) are added and incubated for 72 hours in serum-free medium. For carcinoma cell lines, 3 × 103 cells/well are plated overnight in full growth medium. Linifanib is added to the cells in full growth medium and incubated for 72 hours. For leukemia cells, generally 5 × 104 per well are plated in full growth medium, Linifanib is added, and incubated for 72 hours. The effects on proliferation are determined by addition of Alamar Blue (final solution, 10%), incubation for 4 hours at 37 °C in a CO2 incubator and analysis in a fluorescence plate reader (544 nm, excitation: 590 nm, emission(Only for Reference) |
| 激酶实验 | Kinase assays: Potencies (IC50 values) are determined by assays of active kinase domains cloned and expressed in baculovirus using the FastBacbaculovirus expression system or obtained commercially. For tyrosine kinase assays, a biotinylated peptide substrate containing a single tyrosine is used with 1 mM ATP, anEu-cryptate–labeled anti-phosphotyrosine antibody (PT66), and Strepavidin-APC in a homogeneous time-resolved fluorescence assay. Serine/threonine kinases are assayed using 5 μM ATP, [33P]ATP, and a biotinylated peptide substrate with peptide capture and incorporation of 33P determined using a SA-Flashplate. Linifanib is assayed at multiple concentrations prepared by serial dilution of a DMSO stock solution of Linifanib. The concentration resulting in 50% inhibition of activity is calculated using nonlinear regression analysis of the concentration response data. |
| 体外活性 | 在肺组织中,Linifanib（0.3 mg/kg）使血管内皮生长因子受体磷酸化被完全抑制.在角膜上,每天两次 Linifanib（7.5/15 mg/kg）显著抑制重组碱性成纤维细胞生长因子-和血管内皮生长因子诱导的血管生成.在MDA-231移植瘤中,Linifanib（12.5 mg/kg,2次/天）可降低微脉管密度.Linifanib也抑制水肿反应（ED50：0.5 mg/kg）.作用于移植瘤模型,包括HT1080, H526, MX-1和DLD-1时,Linifanib抑制肿瘤生长（ED75：4.5-12 mg/kg）.作用于在HT1080纤维肉瘤模型中,Linifanib的Cmax和AUC24小时分别为0.4 μg/mL和2.7 μg·hour/mL. |
| 体内活性 | ABT-869对血管内皮生长因子-刺激的人脐动脉内皮细胞增殖有抑制作用（IC50：0.2 nM）。在激酶实验中,Linifanib抑制Kit（IC50：14 nM）、PDGFRβ（IC50：66 nM）和Flt4（IC50：190 nM）。Linifanib也抑制细胞水平配体诱导的KDR（IC50：2 nM）、PDGFR-β（IC50：2 nM）、KIT（IC50：31 nM）和CSF-1R（IC50：10 nM）磷酸化,血清蛋白可影响该效力。在Ba/F3 FLT3 ITD细胞中,Linifanib（10 nM）降低Akt在Ser473位点磷酸化及GSK3β在Ser9位点磷酸化。然而,ABT-869几乎不影响不受血管内皮生长因子或血小板衍生因子诱导的肿瘤细胞,除MV4-11白血病细胞(具有组成型活性形式Flt3,IC50：4 nM)。Linifanib可与CSF-1R的ATP结合位点结合（Ki：3 nM）。 |
| 存储条件 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
| 溶解度 | Ethanol : < 1 mg/mL (insoluble or slightly soluble)
DMSO : 40 mg/mL (106.55 mM)
H2O : < 1 mg/mL (insoluble or slightly soluble)
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| 关键字 | c-Fms | antitumor | CSF-1 receptor | Cluster of differentiation antigen 135 | PDGFR | CD135 | proliferation | ABT869 | RG 3635 | CSF1R | Autophagy | c-Kit | VEGFR | AL 39324 | SCFR | RG-3635 | cell | CSF-1R | Fms like tyrosine kinase 3 | Vascular endothelial growth factor receptor | FLT3 | ABT 869 | Apoptosis | inhibit | Platelet-derived growth factor receptor | colony stimulating factor 1 receptor | AL39324 | cytotoxicity | Inhibitor | microRNA | CD117 | Linifanib |
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| 相关库 | 抑制剂库 | 抗癌活性化合物库 | 已知活性化合物库 | 激酶抑制剂库 | 抗衰老化合物库 | 膜蛋白靶向化合物库 | 酪氨酸激酶分子库 | 药物功能重定位化合物库 | 抗癌临床化合物库 | 抗癌药物库 |