S81434 |
PURVALANOL A |
源叶(MedMol) | 98% |
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- 产品描述: Purvalanol A is a potent CDK inhibitor, which inhibits cdc2-cyclin B, cdk2-cyclin A, cdk2-cyclin E, cdk4-cyclin D1, and cdk5-p35 with IC50s of 4, 70, 35, 850, 75 nM, resepctively.
- 靶点: cdc2-cyclin B:4 nM (IC50);cdk2-cyclin E:35 nM (IC50);cdk2-cyclin A:70 nM (IC50);cdk4-cyclin D1:850 nM (IC50);cdk5-p35:75 nM (IC50);erk1:9000 nM (IC50);Apoptosis; CDK; Autophagy
- 参考文献:
1. Gray NS, et al. Exploiting chemical libraries, structure, and genomics in the search for kinase inhibitors. Science. 1998 Jul 24;281(5376):533-8. 2. Bain J, et al. The specificities of protein kinase inhibitors: an update. Biochem J. 2003 Apr 1;371(Pt 1):199-204. 3. Villerbu N, et al. Cellular effects of purvalanol A: a specific inhibitor of cyclin-dependent kinase activities. Int J Cancer. 2002 Feb 20;97(6):761-9.
- 溶解性: DMSO : ≥ 50 mg/mL (128.57 mM)
- 保存条件: -20℃
- 配置溶液浓度参考:
1mg 5mg 10mg 1 mM 2.571 ml 12.857 ml 25.714 ml 5 mM 0.514 ml 2.571 ml 5.143 ml 10 mM 0.257 ml 1.286 ml 2.571 ml 50 mM 0.051 ml 0.257 ml 0.514 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。
输入产品批号:
本计算器可帮助您计算出特定溶液中溶质的质量、溶液浓度和体积之间的关系,公式为:
质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)