计算溶液所需的质量、体积或浓度。
,适用于对基线干扰要求严格的色谱和分析工作流程。
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在色谱分析、有机合成和交叉偶联反应领域已被 0 篇同行评审文献引用。
Pazopanib HCl (GW786034 HCl)是一种新型的针对VEGFR-1, VEGFR-2, VEGFR-3, PDGFR, FGFR, c-Kit和c-fms等多个靶点的抑制剂,IC50分别是10 nM, 30 nM, 47 nM, 84 nM, 74 nM, 140 nM和146 nM。A multi-targeted inhibitor.
Information
Pazopanib HCl (GW786034 HCl) is a novel multi-target inhibitor ofVEGFR1,VEGFR2,VEGFR3, PDGFR, FGFR, c-Kit and c-Fms withIC50of 10 nM, 30 nM, 47 nM, 84 nM, 74 nM, 140 nM and 146 nM in cell-free assays, respectively. Pazopanib induces autophagic Type II cel
In vitro
Pazopanib potently inhibits VEGF-induced phosphorylation of VEGFR2 in HUVEC cells with IC50 of 8 nM. Pazopanib shows dose-dependent growth inhibition in all synovial sarcoma cell lines including SYO-1 and HS-SY-II cells. Proliferation of SYO-1 and HS-SY-II cells is inhibited even at 1\u2009µg/mL of Pazopanib and is completely abolished at 5\u2009µg/mL. Pazopanib induces G1 arrest, and thereby suppresses the growth of synovial sarcoma cells. Phosphorylation of Akts, GSK-3β, JNKs, p70 S6 Kinase, and mTOR is suppressed in Pazopanib-treated SYO-1 cells compared with that in the vehicle-treated cells. Pazopanib between 20 m g/mL and 22.5 m g/mL shows an increasing reduction of RPE cell viability.
In vivo
The mice treated with 30 mg/kg or 100\u2009mg/kg Pazopanib reveals a significant decrease in tumor burden compared with the mice treated with vehicle or 10\u2009mg/kg Pazopanib. Treatment with Pazopanib is well-tolerated and there is no significant difference in the body weight among the mice in each group.
Cell Data
cell lines:
Concentrations:0-10 μM
Incubation Time:1 hour
Powder Purity:≥99%
H351: 怀疑引起遗传缺陷
H411: 对水生生物有毒并具有长期持续影响
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H361: 怀疑破坏生育力或未出生的孩子
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