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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
- CAS号:
422513-13-1
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥909.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥363.0 |
| 规格: | 5 mg | 产品价格: | ¥800.0 |
| 规格: | 10 mg | 产品价格: | ¥1320.0 |
| 规格: | 25 mg | 产品价格: | ¥2640.0 |
| 规格: | 50 mg | 产品价格: | ¥4200.0 |
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Hesperadin
CAS No. : 422513-13-1
MCE 国际站:Hesperadin
产品活性:Hesperadin 是 Aurora A 和 B 的 ATP 竞争性吲哚酮抑制剂。Hesperadin 以 250 nM 的 IC50 抑制 Aurora B。Hesperadin 通过阻断核分裂和胞质分裂而抑制布鲁氏锥虫的生长。Hesperadin 也是一种广谱流感抗病毒剂。
研究领域:Cell Cycle/DNA Damage | Epigenetics | Autophagy | Anti-infection
作用靶点:Aurora Kinase | Autophagy | Influenza Virus | Parasite
In Vitro: Hesperadin (10-100 nM) inhibits the Aurora kinase-1 (TbAUK1)-mediated phosphoryation of trypanosome histone H3 (TbH3) in a dose dependent manner, with an IC50 of 40 nM.
Hesperadin (0.01-10 μM; 24 or 48 hours) inhibits growth of bloodstream forms (BF) and procyclic forms (PF) cultures.
Hesperadin (100-200 nM; 24-72 hours) alters cell morphology and inhibits cell cycle progression similar to the RNAi knockdown of TbAUK1.
In Vivo: Hesperadin (20 mg/kg/d; i.v.) prolongs the survival of xenograft mice via synergistic effect with temozolomide (TMZ).
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