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FR 180204

 
Catalog No.
A8304
ERK inhibitor
组合的产品项目
规格价格库存 数量
10mM (in 1mL DMSO)
¥ 863.00
Ship with 10-15 days
10mg
¥ 1,481.00
Ship with 10-15 days
50mg
¥ 6,290.00
Ship with 10-15 days

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A

背景

Selective ERK inhibitor (IC50 values are 0.14 and 0.31 μM for ERK2 and ERK1 respectively). Displays 30-fold selectivity for ERK over p38α (IC50 = 10 μM); displays no activity against human recombinant MEK1, MKK4, IKKα, PKCα, Src, Syc and PDGFα at concentrations less than 30 μM. Also inhibits TGFβ-induced AP-1 activation in Mv1Lu cells (IC50 = 3.1 μM).

文献引用

1. White SM, Avantaggiati ML, et al. "YAP/TAZ Inhibition Induces Metabolic and Signaling Rewiring Resulting in Targetable Vulnerabilities in NF2-Deficient Tumor Cells." Dev Cell. 2019 May 6;49(3):425-443.e9. PMID:31063758

化学属性

Physical AppearanceA solid
StorageStore at -20°C
M.Wt327.34
Cas No.865362-74-9
FormulaC18H13N7
Solubilityinsoluble in H2O; ≥10.25 mg/mL in DMSO; ≥4.47 mg/mL in EtOH with ultrasonic
Chemical Name5-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)-1H-pyrazolo[3,4-c]pyridazin-3-amine
SDFDownload SDF
Canonical SMILESC1=CC=C(C=C1)C2=NN3C=CC=CC3=C2C4=NN=C5C(=C4)C(=NN5)N
运输条件 蓝冰运输或根据您的需求运输。
一般建议不同厂家不同批次产品溶解度各有差异,仅做参考。若实验所需浓度过大至产品溶解极限,请添加助溶剂助溶或自行调整浓度。溶液形式一般不宜长期储存,请尽快用完。

质量控制

化学结构

FR 180204