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- 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 |
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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
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