Belvarafenib TFA(Synonyms: HM95573 TFA; GDC-5573 TFA; RG6185 TFA)

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Belvarafenib TFA (Synonyms: HM95573 TFA; GDC-5573 TFA; RG6185 TFA) 纯度: ≥99.0%

Belvarafenib TFA (HM95573 TFA) 是一种有效的,广泛的迅速加速纤维肉瘤激酶 (RAF) 的抑制剂,其对 B-RAF,B-RAFv600E 和C-RAF 的 IC50 值分别为 56 nM, 7 nM 和 5 nM。

Belvarafenib TFA(Synonyms: HM95573 TFA; GDC-5573 TFA; RG6185 TFA)

Belvarafenib TFA Chemical Structure

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Belvarafenib TFA 的其他形式现货产品:

Belvarafenib

生物活性

Belvarafenib TFA (HM95573 TFA) is a potent and pan RAF (Rapidly Accelerated Fibrosarcoma) inhibitor, with IC50s of 56 nM, 7 nM and 5 nM for B-RAF, B-RAFv600E and C-RAF respectively[1].

IC50 & Target

IC50: 56 nM(B-RAF), 7 nM(B-RAFv600E), 5 nM(C-RAF)[1].

体外研究
(In Vitro)

Belvarafenib (Example 116) is a potent and pan RAF inhibitor with antineoplastic activity. The IC50 values of Belvarafenib are 56 nM, 7 nM and 5 nM for B-RAF, B-RAFv600E and C-RAF respectively. It also shows high inhibitory activity for FMS, DDR1 and DDR2 kinases, with IC50s of 10 nM, 23 nM and 44 nM, respectively[1].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

Clinical Trial

分子量

592.95

Formula

C25H17ClF4N6O3S

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

-20°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

参考文献
  • [1]. WO 2013/100632 A1.

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