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GW806742X hydrochloride

カタログ番号GC61454

GW806742X 塩酸塩は、ATP 模倣薬であり、強力な MLKL (Mixed Lineage Kinase Domain-Like protein) 阻害剤であり、9.3 μM の Kd で MLKL シュードキナーゼ ドメインに結合します。 GW806742X 塩酸塩は、VEGFR2 に対して活性があります (IC50=2 nM)。 GW806742X 塩酸塩は MLKL 膜移行を遅らせ、ネクロトーシスを阻害します。

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GW806742X hydrochloride 化学構造

サイズ 価格 在庫数 個数
10mM (in 1mL DMSO)
$75.00
在庫あり
5 mg
$56.00
在庫あり
10 mg
$74.00
在庫あり
25 mg
$139.00
在庫あり
50 mg
$232.00
在庫あり
100 mg
$417.00
在庫あり

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

GW806742X hydrochloride, an ATP mimetic and a potent MLKL (Mixed Lineage Kinase Domain-Like protein) inhibitor, binds the MLKL pseudokinase domain with a Kd of 9.3 μM. GW806742X hydrochloride has activity against VEGFR2 (IC50=2 nM). GW806742X hydrochloride retards MLKL membrane translocation and inhibits necroptosis[1][2].

GW806742X (0.1-10000 nM) inhibits necroptotic death of wild-type mouse dermal fibroblasts (MDFs) stimulated with TSQ (1 ng/mL TNF, 500 nM compound A (Smac mimetic), 10 μM Q-VD-OPh) in a dose-dependent manner[1].GW806742X shows inhibition of VEGF induced proliferation of HUVECs with an IC50 of 5 nM[2].

[1]. Hildebrand JM, et al. Activation of the pseudokinase MLKL unleashes the four-helix bundle domain to induce membrane localization and necroptotic cell death. Proc Natl Acad Sci U S A. 2014;111(42):15072-15077. [2]. Sammond DM, et al. Discovery of a novel and potent series of dianilinopyrimidineurea and urea isostere inhibitors of VEGFR2 tyrosine kinase. Bioorg Med Chem Lett. 2005;15(15):3519-3523.

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Average Rating: 5 ★★★★★ (Based on Reviews and 18 reference(s) in Google Scholar.)

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