GAK inhibitor 49 hydrochloride
目录号: PL02705 纯度: ≥98%
商品编号 规格 价格 会员价 是否有货 数量
PL02705-5mg 5mg ¥2472.73 请登录
PL02705-10mg 10mg ¥4327.27 请登录
PL02705-25mg 25mg ¥8036.36 请登录
PL02705-50mg 50mg ¥11745.45 请登录
PL02705-100mg 100mg ¥16690.91 请登录
PL02705-200mg 200mg 询价 询价
PL02705-500mg 500mg 询价 询价
PL02705-10mM*1mLinDMSO 10mM*1mLinDMSO ¥2720.00 请登录
Medlife所售产品仅用于科学研究(非临床研究),非药品不可食用,不可用于人体或动物的临床诊断和治疗,我们不为个人提供产品及服务。产品COA等资料,可至下方“质量控制”中下载。
中文名称
GAK inhibitor 49 hydrochloride
英文名称
GAK inhibitor 49 hydrochloride
包装储存
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
产品详情
GAK inhibitor 49 hydrochloride 是一种 ATP 竞争性的、高选择性细胞周期蛋白G相关激酶 (GAK) 抑制剂,Ki 为 0.54 nM,细胞 IC50 为 56 nM。GAK inhibitor 49 hydrochloride 也显示与 RIPK2 结合。
生物活性
GAK inhibitor 49 hydrochloride is a potent, ATP-competitive and highly selective cyclin G associated kinase (GAK) inhibitor with a K i of 0.54 nM and a cell IC 50 of 56 nM. GAK inhibitor 49 hydrochloride also shows binding to RIPK2.
性状
Solid
体外研究(In Vitro)
GAK inhibitor 49 (compound 49) hydrochloride shows a weak inhibitory effect on AAK1, BMP2K and STK16, with IC50s of 28, 63 and >100μM, respectively. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
参考文献
[1]. Asquith CRM, et al. Identification and Optimization of 4-Anilinoquinolines as Inhibitors of Cyclin G Associated Kinase. ChemMedChem. 2018;13(1):48-66.
溶解度数据
In Vitro: DMSO : 14.29 mg/mL (35.12 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2