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AG 494

    
99.70%

N-Phenyl-3,4-Dihydroxybenzylidenecyanoacetamide

源叶(MedMol)
S88020 一键复制产品信息
133550-35-3
C16H14N2O3
282.29
酪氨酸激酶抑制剂 AG 494
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S88020-5mg买3赠1
99.70%

¥150.00

9 - - - -
S88020-10mg买3赠1
99.70%

¥260.00

>10 - - - -
S88020-50mg促销
99.70%

¥490.00 ¥392.00

6 - - - -
S88020-100mg促销
99.70%

¥860.00 ¥688.00

5 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: AG-494 (Tyrphostin AG 494) is a potent and selective EGFR tyrosine kinase inhibitor (IC50=0.7 μM). AG-494 inhibits the autophosphorylation of EGFR, ErbB2, HER1-2 and PDGF-R with IC50s 1.1, 39, 45 and 6 μM, respectively. AG-494 blocks Cdk2 activation and inhibits EGF-dependent DNA synthesis
靶点: EGFR:0.7 μM (IC50);EGFR; CDK
参考文献: 1. Gazit A, et al. Tyrphostins. 2. Heterocyclic and alpha-substituted benzylidenemalononitrile tyrphostins as potent inhibitors of EGF receptor and ErbB2/neu tyrosine kinases. J Med Chem. 1991;34(6):1896-1907. 2. Osherov N, et al. Tyrphostin AG 494 blocks Cdk2 activation. FEBS Lett. 1997;410(2-3):187-190. 3. Osherov N, et al. Selective inhibition of the epidermal growth factor and HER2/neu receptors by tyrphostins. J Biol Chem. 1993 May 25;268(15):11134-42. 4. Liu X, Qin J, et al. Cross-talk between EGF and BMP9 signalling pathways regulates the osteogenic differentiation of mesenchymal stem cells. J Cell Mol Med. 2013;17(9):1160-1172. 5. Jihee Lee Kang, et al. SILICA-INDUCED NUCLEAR FACTOR- k B ACTIVATION: INVOLVEMENT OF REACTIVE OXYGEN SPECIES AND PROTEIN TYROSINE KINASE ACTIVATION. Journal of Toxicology and Environmental Health, Part A.
溶解性: Soluble  in  DMSO
保存条件: 2-8℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 3.542 ml 17.712 ml 35.425 ml
5 mM 0.708 ml 3.542 ml 7.085 ml
10 mM 0.354 ml 1.771 ml 3.542 ml
50 mM 0.071 ml 0.354 ml 0.708 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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