BFH772 ≥98%(HPLC)
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| 包装规格: | 2mg 5mg 10mg 25mg 50mg 100mg in glass bottle |
| 产品简介: | 是一种有效的,具有口服活性的 VEGFR2 抑制剂,IC50 为 3 nM。 |
| 溶解性: | 溶于DMSO(87 mg/mL )和乙醇 |
| 储备液保存: | -80°C, 2 years -20°C, 1 year |
| 体内实验: | 1、请依序添加每种溶剂: 10% DMSO→90% Corn Oil Solubility: ≥ 2.5 mg/mL (5.69 mM); 澄清溶液 此方案可获得 ≥ 2.5 mg/mL(饱和度未知)的澄清溶液,此方案实验周期在半个月以上的动物实验酌情使用。 以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。 <1mg/ml表示微溶或不溶。 普西唐提供的所有化合物浓度为内部测试所得,实际溶液度可能与公布值有所偏差,属于正常的批间细微差异现象。 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;⼀旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 |
| 靶点: | VEGFR2 3 nM (IC50) |
| 体外研究: | BFH772 is highly selective; apart from inhibiting VEGFR2 at 3 nM IC50, it also targets B-RAF, RET, and TIE-2, albeit with at least 40-fold lower potency. BFH772 is inactive (IC50>10 μM; >2 μM for cKIT) against all other tyrosine specific- and serine/threonine-specific protein kinases tested. BFH772 inhibits VEGFR2 with IC50 of 4.6±0.6 nM in CHO cells. BFH772 inhibits VEGFR2 with IC50 of 3 nM in HUVEC cells. BFH772 inhibits the ligand induced autophosphorylation of RET, PDGFR, and KIT kinases, with IC50 values ranging between 30 and 160 nM. BFH772 is selective (IC50 values >0.5 μM) against the kinases of EGFR, ERBB2, INS-R, and IGF-1R and against the cytoplasmic BCR-ABL kinase. IC50 of BFH772 (<0.01 nM, n=2) demonstrates that they abrogated VEGF induced proliferation at remarkably low nM concentrations. |
| 体内研究: | BFH772 at 3 mg/kg orally dosed once per day potently inhibits melanoma growth (by 54-90% for primary tumor and 71-96% for metastasis growth) as depicted by treatment to control ratios. Dose–response curves of BFH772 at 0.3, 1, and 3 mg/kg demonstrate that even at the lowest concentrations, this naphthalene-1-carboxamide inhibits VEGF induced tissue weight and TIE-2 levels but only reaches statistical significance at 1 mg/kg and above. |
| 细胞实验: | 细胞系:HUVEC内皮细胞 浓度:0-10 nM 处理时间:48 h 方法:将半融合状态的HUVECs接种于96孔板,用含1.5% FCS和固定浓度的VEGF(10 ng/mL),bFGF (0.5 ng/mL)或bFGF (0.5 ng/mL)、及检测化合物的基础培养基进行培养。24小时后,加入BrdU标记溶液,再将细胞继续培养24小时,然后固定、封闭、加anti-BrdU抗体进行染色。 |
| 动物实验: | 动物模型:Sprague−Dawley大鼠 剂量:1 mg/kg 给药处理:静脉注射 |
| 保存条件: | -20℃ |
| 注意事项: | 1、为了您的安全和健康,请穿实验服并戴一次性手套操作。 2、以上信息仅做参考交流之用。 |
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