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- 详细信息
- 技术资料
- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- 规格:
10 mM * 1 mL/5 mg/10 mg/25 mg/50 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥935.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥850.0 |
| 规格: | 10 mg | 产品价格: | ¥1200.0 |
| 规格: | 25 mg | 产品价格: | ¥2500.0 |
| 规格: | 50 mg | 产品价格: | ¥4200.0 |
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Ningetinib
CAS No. : 1394820-69-9
MCE 国际站:Ningetinib
产品活性:Ningetinib 是一种有效的口服生物可用的小分子酪氨酸激酶抑制剂 (TKI),对 c-Met,VEGFR2 和 Axl 的 IC50 值分别为 6.7, 1.9 和 <1.0 nM。
研究领域:Protein Tyrosine Kinase/RTK
作用靶点:TAM Receptor | VEGFR | c-Met/HGFR
In Vitro: Ningetinib is a potent, orally bioavailable small molecule tyrosine kinase inhibitor (TKI) with IC50s of 6.7, 1.9 and <1.0 nM for c-Met, VEGFR2 and Axl, respectively. In cell-based functional assays, Ningetinib (CT053PTSA) inhibits HGF and VEGF-stimulated HUVEC proliferation and microvascular angiogenesis in rat aortic rings with IC50 values of 8.6 and 6.3 nM, respectively.
In Vivo: When single dosed orally (3 mg/kg) to U87MG tumor-bearing nude mice, Ningetinib (CT053PTSA) potently inhibits the phosphorylation of c-Met and its downstream signaling kinases AKT and ERK1/2 for up to 6 hours in tumor tissues. In orthotopic U87MG human glioblastoma xenograft model, Ningetinib prolongs the median survival time (MST) and yields significant increase in life-span value (ILS=32%, p=0.003) at an oral dose of 20 mg/kg/day (dosed 21 days) versus the vehicle-treated group.
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