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RIPK1-IN-7
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
RIPK1-IN-7图片
CAS NO:2300982-44-7
包装与价格:
包装价格(元)
1 mg电议
5 mg电议
10 mg电议
25 mg电议
50 mg电议
100 mg电议
200 mg电议
500 mg电议
1 mL*10 mM(in DMSO)电议

产品介绍
RIPK1-IN-7 是一种选择性有效的 RIPK1 抑制剂,Kd值为 4 nM,IC50值为 11 nM。在实验性 B16 黑色素瘤肺转移模型中表现出优异的抗转移活性。

产品描述

RIPK1-IN-7 is a potent and selective inhibitor of RIPK1(Kd of 4 nM and an enzymatic IC50 of 11 nM),andexhibits excellent antimetastasis activity in the experimental B16 melanoma lung metastasis model.

体外活性

In the TSZ-induced HT29 cell necroptosis model, RIPK1-IN-7 shows potent cell protection effect (EC50 of 2nM). RIPK1-IN-7 displays considerable activity against several other kinases(Flt4, TrkA, TrkB, TrkC, Axl, HRI, Mer, and MAP4K5 with IC50s of 20, 26, 8, 7, 35, 26, 29, and 27 nM, respectively).

Cas No.

2300982-44-7

分子式

C25H22F3N5O2

分子量

481.47

储存和溶解度

DMSO:60 mg/mL (124.62 mM),Need ultrasonic
H2O:0.1 mg/mL (insoluble)
Powder: -20°C for 3 years
In solvent: -80°C for 2 years