CAS NO: | 835621-07-3 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 |
Regorafenib Hydrochloride (BAY 73-4506 hydrochloride) is a multi-target inhibitor forVEGFR1/2/3,PDGFRβ,Kit,RETandRaf-1withIC50s of 13/4.2/46, 22, 7, 1.5 and 2.5 nM, respectively[1]. |
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IC50& Target[1] |
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体外研究 (In Vitro) |
Regorafenib potently inhibits VEGFR2 autophosphorylation in NIH-3T3/VEGFR2 cells with an IC50of 3 nM. In HAoSMCs, regorafenib inhibits PDGFR-β autophosphorylation after stimulation with PDGF-BB, with an IC50of 90 nM. Regorafenib inhibits the proliferation of VEGF165-stimulated HUVECs, with an IC50of 3 nM[1]. Regorafenib causes a concentration-dependent decrease in Hep3B cell growth, having an IC50of 5 μM. Regorafenib subsequently increases the levels of phospho-c-Jun, a JNK target, but not total c-Jun in Hep3B cells[3].
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体内研究 (In Vivo) |
Regorafenib effectively inhibits growth of the Colo-205 xenografts in the dose range of 10-100 mg/kg reaching a TGI of 75% at day 14 at the 10 mg/kg dose. In the MDA-MB-231 model, regorafenib is highly efficacious at a dose as low as 3 mg/kg, resulting in a significant TGI of 81%, which increases to 93% at doses of 10 and 30 mg/kg, where tumor stasis is reached[1].
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Clinical Trial |
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分子量 |
519.28 |
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性状 |
Solid |
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Formula |
C21H16Cl2F4N4O3 |
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CAS 号 |
835621-07-3 |
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中文名称 |
瑞戈非尼盐酸盐;瑞格菲尼盐酸盐 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) |
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溶解性数据 |
In Vitro:
DMSO : ≥ 5.6 mg/mL(10.78 mM) H2O :< 0.1 mg/mL(insoluble) *"≥" means soluble, but saturation unknown.
配制储备液
*
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