| CAS: | 548472-68-0 | |||
| 分子式: | C30H30Cl2N4O4 | |||
| 分子量: | 581.49 | |||
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| 用途: | Nutlin-3是一种有效的,选择性的Mdm2(依赖环指状的泛素蛋白连接酶和p53)拮抗剂,IC50为90 nM。可稳定p53缺陷的细胞中的p73。 |
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | |||||||||||||||||||||||||||||||||||||||||||
| N864239 | MACKLIN | Nutlin-3 | ≥98% | 214元/10mg; 760元/50mg; 1315元/100mg; 2288元/250mg; | 咨询 | ||||||||||||||||||||||||||||||||||||||||||
储存:-20°C 状态:白色固体 | |||||||||||||||||||||||||||||||||||||||||||||||
| N1195 | TCI | Nutlin-3 | >95.0%(HPLC) | 1100元/10MG; 3990元/50MG; | 咨询 | ||||||||||||||||||||||||||||||||||||||||||
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| 444143 | Sigma-Aldrich | MDM2 Antagonist, Nutlin-3, Racemic-CAS 548472-68-0-Calbiochem | The MDM2 Antagonist, Nutlin-3, Racemic, also referenced under CAS 548472-68-0, controls the biological activity of MDM2. This small molecule/inhibitor is primarily used for Cancer applications. | 1903.37元/1 MG; | 咨询 | ||||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 A cell-permeable cis-imidazoline compound that acts as a potent and selective MDM2 antagonist (IC50 = 90 nM for Nutlin-3a and 13.6 µM for Nutlin-3b) and displays antitumor properties. Activates p53 pathway by binding MDM2 in the p53-binding pocket and inhibits MDM2-p53 interaction. Shown to suppress tumor growth by induction of apoptosis in several cancer cells with wild-type p53 and in xenografted tumor mice. A 10 mM (1 mg/172 µl) solution of MDM2 Antagonist, Nutlin-3, Racemic (Cat. No. 444151) in DMSO is also available. 包装 1 mg in Plastic ampoule 生化/生理作用 Cell permeable: yes 警告 Toxicity: Harmful (C) 重悬 Following reconstitution, aliquot, purge with inert gas, and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C. 其他说明 Thompson, T., et al. 2004. J. Biol. Chem.279, 53015. 法律信息 CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany 基本信息
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| N6287 | Sigma-Aldrich | Nutlin-3 | ≥98% (HPLC), powder | 1505.41元/1 MG; 5223.7元/5 MG; | 咨询 | ||||||||||||||||||||||||||||||||||||||||||
产品说明 应用 Nutlin-3可用于:
包装 1, 5 mg in glass bottle 生化/生理作用 Nutlin-3是小鼠双微体基因2人同源基因(HDM2)的拮抗剂,具有抑制 HDM2 介导 p53 基因降解的能力。Nutlin-3 还可以增强 p73 基因的转录活性。 特点和优势 该化合物由 Roche 开发。要浏览其他制药公司开发的化合物列表批准的药物/候选药物的列表, 点击这里 。 其他说明 相对立体化学; (4R,5S)和(4S,5R)对映异构体的外消旋混合物。 分析说明 相对立体化学 法律信息 经 Hoffman-La Roche,Inc 许可销售,美国专利 6,734,302。 基本信息
产品性质
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