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merck millipore,默克密理博,217713,Cdk1/2 Inhibitor II, NU6102 - CAS 444722-95-6 - Calbiochem
产品名称:Cdk1/2 Inhibitor II, NU6102 - CAS 444722-95-6 - Calbiochem
产品型号:217713
The Cdk1/2 Inhibitor II, NU6102, also referenced under CAS 444722-95-6, controls the biological activity of Cdk1/2. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylat More>>
merck millipore,默克密理博,217713,Cdk1/2 Inhibitor II, NU6102 - CAS 444722-95-6 - Calbiochem
- 产品介绍
重要规格表
经验配方 CAS号 C₁₈H₂₂N₆O₃S 444722-95-6 描述 概述 A cell-permeable 2,6-disubstituted purine compound that displays antiproliferative properties. Acts as a potent and ATP-competitive inhibitor of Cdk1/cyclin B and Cdk2/cyclin A3 (IC50 = 9.5 nM and 5.4 nM). Displays greater selectivity for Cdk1/2 over other kinases tested (IC50 = 600 nM, 800 nM, 900 nM and 1.6 µM for ROCKII, PDK1, DYRK1A and Cdk4/D1, respectively). Shown to inhibit human MCF-7 breast carcinoma cell growth with a GI50 of 8 µM. 产品目录编号 217713 品牌系列 Calbiochem®
同义词 6-Cyclohexylmethoxy-2-(4ʹ-sulfamoylanilino)purine 参考 参考 Hardcastle, I.R., et al. 2004. J. Med. Chem. 47, 3710.
Sayle, K.L., et al. 2003. Bioorg. Med. Chem. Lett. 13, 3079.
Davies, T.G., et al. 2002. Nat. Struct. Biol. 9, 745.产品信息 CAS号 444722-95-6 具有ATP竞争性 Y 形式 White solid Hill配方 C₁₈H₂₂N₆O₃S 化学配方 C₁₈H₂₂N₆O₃S Molar Mass 402.5 可逆 N 结构配方图像 生物信息 主靶 Cdk1/cyclin B, Cdk2/cyclin A3 主靶IC50 9.5 nM, 5.4 nM against Cdk1/cyclin B, Cdk2/cyclin A3, respectively 纯度 ≥95% by HPLC 理化信息 细胞可渗透 Y 溶解度 DMSO 储存和货运信息 货运代码 Ambient Temperature Only
毒性 Carcinogenic / Teratogenic
储存 +2°C to +8°C
避光 Protect from light
无需冷冻 No
特殊指南 Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C. 包装信息 惰性气体下包装 Packaged under inert gas
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