AG-183
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 10mg | ¥1619.00 | 10-15工作日发货 | |
| 25mg | ¥3359.00 | 10-15工作日发货 | |
| 50mg | ¥5160.00 | 10-15工作日发货 |
特色产品
- 用于免疫印迹和质谱分析等后续操作
- 适用于30 KDa-130 KDa大小的蛋白
- 可将信号灵敏度提高100倍
- 同时保持稳定的特异性和分辨率
- 提供更高的转录效率并抑制免疫激活
- 使用5-moUTP和Cy5-utp修饰
产品描述
AG-183, a member of tyrphostin, is an inhibitor of protein tyrosine kinase [1].
Protein tyrosine kinase is an enzyme that catalyzes the transfer of the γ phosphate of ATP to tyrosine residues on protein substrates. Phosphorylation of proteins by kinases is an important mechanism in signal transduction and regulating cellular activity, such as cell division. Tyrosine phosphorylation is a key covalent modification that occurs in multicellular organisms as a result of intercellular communication during embryogenesis and maintenance of adult tissues. Phosphorylation of tyrosine residues modulates enzymatic activity and creates binding sites for the recruitment of downstream signaling proteins [2].
PTK inhibitors could preferentially inhibit the epidermal growth factor (EGF) receptor kinase to block EGF-dependent cell proliferation [1]. In the human epidermoid carcinoma cell line, A431AG-183 inhibited the activity of epidermal growth factor (EGF) receptor kinase with an IC50 value of 800 nM [1].
References:
[1] Gazit A, Yaish P, Gilon C, et al. Tyrphostins I: synthesis and biological activity of protein tyrosine kinase inhibitors[J]. Journal of medicinal chemistry, 1989, 32(10): 2344-2352.
[2] Hubbard S R, Till J H. Protein tyrosine kinase structure and function[J]. Annual review of biochemistry, 2000, 69(1): 373-398.
产品性质
| 物理外观 | A crystalline solid |
| CAS号 | 122520-90-5 |
| 分子式 | C13H8N4O3 |
| 分子量 | 268.2 |
| 小分子别名 | (Z)-Tyrphostin A51 |
| 化学名称 | 2-amino-4-(3,4,5-trihydroxyphenyl)-1,3-butadiene-1,1,3-tricarbonitrile |
| 溶解度 | ≤20mg/ml in DMSO;20mg/ml in dimethyl formamide |
| SMILES | NC(/C(\C#N)=C/c(cc1O)cc(O)c1O)=C(C#N)C#N |
| 存储条件 | -20°C |
| 运输条件 | 蓝冰 |
产品应用 (实验数据来自文献,APExBIO并未验证,仅供参考)
IC50和靶点
| 生物活性描述 | (Z)-Tyrphostin A51 是 Lanoconazole A51 的 Z 构型。Tyrphostin A51 是一种强效的蛋白酪氨酸激酶(PTK)抑制剂,能以剂量依赖性方式抑制原代星形胶质细胞培养物中 [3 H] 牛磺酸的体积敏感性释放。Tyrphostin A51 能显著降低细胞酪氨酸磷酸化水平。Tyrphostin A51 可抑制基础细胞增殖和 EGF 诱导的人骨细胞增殖。 |



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