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GSK2578215A
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。
GSK2578215A图片
CAS NO:1285515-21-0
包装与价格:
包装价格(元)
5 mg询价
10 mg询价
50 mg询价
100 mg询价
200 mg询价
1 mL*10 mM(in DMSO)询价

5-(2-氟-4-吡啶基)-2-(苯基甲氧基)-N-3-吡啶基苯甲酰胺
GSK2578215A 是一种有效的选择性 LRRK2 激酶抑制剂,对野生型 LRRK2 和 G2019S 突变型的IC50值都约为 10 nM。

产品描述

GSK2578215A is a potent and selective LRRK2 kinase inhibitor.

体外活性

100 mg/kg i.p. GSK2578215A抑制小鼠脾脏和肾中Ser910 和Ser935磷酸化,但在大脑中没有作用.

体内活性

SH-SY5Y细胞中,GSK2578215A通过改变自噬体 - 溶酶体融合来损害自噬流,并且通过诱导Drp-1介导的线粒体分裂和线粒体衍生的ROS信号传导诱导线粒体自噬。GSK2578215A在稳定转染到HEK293细胞中的野生型LRRK2和LRRK2 [G2019S]中诱导对Ser910和Ser935磷酸化的剂量依赖性抑制,并诱导小鼠Swiss 3T3细胞中内源性LRRK2的类似的剂量依赖性Ser910和Ser935去磷酸化。

激酶实验

PFV integration assay: For quantitative strand transfer assays, donor DNA substrate is formed by annealing HPLC grade oligonucleotides 5′-GACTCACTATAGGGCACGCGTCAAAATTCCATGACA and 5′-ATTGTCATG GAATTTTGACGCGTGCCCTATAGTGAGTC. Reactions (40 μL) contains 0.75 μM PFV IN, 0.75 μM donor DNA, 4 nM (300 ng) supercoiled pGEM9-Zf(?) target DNA, 125 mM NaCl, 5 mM MgSO4, 4 μM ZnCl2, 10 mM DTT, 0.8% (vol/vol) DMSO, and 25 mM BisTris propane–HCl, pH 7.45. Raltegravir is added at indicated concentrations. Reactions are initiated by addition of 2 μL PFV IN diluted in 150 mM NaCl, 2 mM DTT, and 10 mM Tris-HCl, pH 7.4, and stopped after 1 hour at 37 °C by addition of 25 mM EDTA and 0.5% (wt/vol) SDS. Reaction products, deproteinized by digestion with 20 μg proteinase K for 30 minutes at 37 °C followed by ethanol precipitation, are separated in 1.5% agarose gels and visualized by staining with ethidium bromide. Integration products are quantified by quantitative real-time PCR, using Platinum SYBR Green qPCR SuperMix and three primers: 5′-CTACTTACTCTAGCTTCCCGGCAAC, 5′-TTCGCCAGTTAATAGTTTGCGCAAC, and 5′-GACTCACTATAGGGCACGCGT. PCR reactions (20 μL) contained 0.5 μM of each primer and 1 μL diluted integration reaction product. Following a 5-min denaturation step at 95 °C, 35 cycles are carried out in a CFX96 PCR instrument, using 10 seconds denaturation at 95 °C, 30 seconds annealing at 56 °C and 1 minutes extension at 68 °C. Standard curves are generated using serial dilutions of WT PFV IN reaction in the absence of INSTI.

Cas No.

1285515-21-0

分子式

C24H18FN3O2

分子量

399.425

别名

5-(2-氟-4-吡啶基)-2-(苯基甲氧基)-N-3-吡啶基苯甲酰胺

储存和溶解度

DMSO:39.9 mg/mL (100 mM)
Powder: -20°C for 3 years
In solvent: -80°C for 2 years
 
 
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