相关产品推荐更多 >
万千商家帮你免费找货
0 人在求购买到急需产品
相关阅读
细胞污染识别与处理全攻略:5 种常见类型+关键误区Cytoscape 教程来了!快速实现顶刊同款通路网络图五大应用案例:Mustang Q 膜层析应用全解析1 个小工具,一次性搞定流程图、质粒图谱和信号通路图- 详细信息
- 文献和实验
- 技术资料
- CAS号:
179248-59-0
- 规格:
1mg/1mLx10mM(inDMSO)/2mg/5mg/10mg/25mg/50mg/100mg/500mg
| 规格: | 1mg | 产品价格: | ¥239.0 |
|---|---|---|---|
| 规格: | 1mLx10mM(inDMSO) | 产品价格: | ¥380.0 |
| 规格: | 2mg | 产品价格: | ¥330.0 |
| 规格: | 5mg | 产品价格: | ¥462.0 |
| 规格: | 10mg | 产品价格: | ¥630.0 |
| 规格: | 25mg | 产品价格: | ¥1464.0 |
| 规格: | 50mg | 产品价格: | ¥2360.0 |
| 规格: | 100mg | 产品价格: | ¥3480.0 |
| 规格: | 500mg | 产品价格: | ¥7304.0 |
Product Introduction
Bioactivity
| 名称 | Src Inhibitor 1 |
| 描述 | Src Inhibitor 1 (Src Kinase Inhibitor 1) is a potent and selective dual site Src tyrosine kinase inhibitor. |
| 激酶实验 | Assays (25.5 μL volume) are carried out robotically at room temperature (21°C) and are linear with respect to time and enzyme concentration under the conditions used. Assays are performed for 30 min using Multidrop Micro reagent dispensers in a 96-well format. The concentration of magnesium acetate in the assays is 10 mM and [γ-33P]ATP (800 c.p.m./pmol) is used at 5, 20 or 50 μM as indicated, in order to be at or below the Kmfor ATP for each enzyme.The assays are initiated with MgATP, stopped by the addition of 5 μL of 0.5 M orthophosphoric acid and spotted on to P81 filter plates using a unifilter harvester. The IC50 values of inhibitors are determined after carrying out assays at ten different concentrations of each compound[2]. |
| 体外活性 | Src-I1在激酶的ATP和肽结合位点具有竞争性作用。其IC50值对Src和Lck分别为44 nM和88 nM[1]。Src-I1是一种强效的Src抑制剂(IC50=0.18 μM),同时也能以类似Src的效力抑制Src家族的其他成员。此外,它对CHK2的抑制效力与对Src相当,而对Aurora B的抑制效力略低[2]。 |
| 存储条件 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
| 溶解度 | DMSO : 14.5 mg/mL (38.83 mM), Sonication is recommended. 10% DMSO+90% (20% SBE-β-CD in Saline) : 0.91 mg/mL (2.44 mM), Solution. |
| 关键字 | Src Kinase Inhibitor-1 | Src Kinase Inhibitor1 | Src Inhibitor-1 | Src Inhibitor1 | Src Inhibitor 1 | Src | Lck | Inhibitor | inhibit |
| 相关产品 | Pelitinib | MCB-613 | Dasatinib monohydrate | SI-2 hydrochloride | Vemurafenib | TAK-901 | Tofacitinib | Staurosporine | Dasatinib | Nintedanib | Ibrutinib | iHCK-37 |
| 相关库 | Inhibitor Library | Bioactive Compound Library | Bioactive Compounds Library Max | Anti-Pancreatic Cancer Compound Library | Anti-Infection Compound Library | Kinase Inhibitor Library | HIF-1 Signaling Pathway Compound Library | Anti-Viral Compound Library | Membrane Protein-targeted Compound Library | Tyrosine Kinase Inhibitor Library | Target-Focused Phenotypic Screening Library | Reprogramming Compound Library |
风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验网络 二、p59 fyn 的 1.p59 fyn 的分布和结构 p59 fyn 为非受体PTKs src家庭的一个成员,见于多种细胞中。由于基因拼接的差异产生了两种不同形式的p59 fyn 。一种以高水平表达于大脑中(p59
网络 九、CD59 CD59是近年(1989)才发现的一种分子量只有18~20kDa的膜性调节蛋白。由Sugita等(1988年)首先描述,曾有不同的名称,如同种限制因子20(homologous restriction factor-20),保护素(protectin)及膜反应性溶破抑制物(membrane inhibitor of reactive
PI4KIII beta inhibitor 3,1245319-54-3新型免疫抑制剂研究概述
PI4KIII beta inhibitor 3是MedChemExpress (MCE) 推出的一种新型、高效的PI4KIIIβ特异性抑制剂,凭借优异的靶向活性与独特的药理作用,成为自身免疫性疾病、炎症性疾病及移植免疫相关研究的重要工具化合物。该化合物靶向性强、活性浓度低,兼具显著的体外免疫抑制活性与体内疾病干预效果,目前已被多项科研研究引用,在基础药理研究与新药研发领域具备广阔的应用前景。 一、产品基础理化参数 PI4KIII beta inhibitor 3为标准化科研级小分子化合物
技术资料暂无技术资料 索取技术资料










