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• 产品描述： GW843682X is a selective, ATP-competitive inhibitor of PLK1 and PLK3, with IC50s of 2.2 nM and 9.1 nM, respectively, and is also >100-fold selective against ∼30 other kinases.

• 靶点： PLK1:2.2 nM (IC50);PLK3:9.1 nM (IC50);PDGFR1β:160 nM (IC50);VEGFR2:360 nM (IC50);Aurora A:4800 nM (IC50);CDK2/cyclin A:7600 nM (IC50);VEGFR;PLK;CDK;PDGFR;AuroraKinase

• 参考文献：
  1. Lansing TJ, et al. In vitro biological activity of a novel small-molecule inhibitor of polo-like kinase 1. Mol Cancer Ther. 2007 Feb;6(2):450-9. Epub 2007 Jan 31. 2. Didier C, et al. Evaluation of Polo-like Kinase 1 inhibition on the G2/M checkpoint in Acute Myelocytic Leukaemia. Eur J Pharmacol. 2008 Sep 4;591(1-3):102-5. 3. Ikezoe T, et al. A novel treatment strategy targeting polo-like kinase 1 in hematological malignancies. Leukemia. 2009 Sep;23(9):1564-76.

• 溶解性： Soluble  in  DMSO

• 保存条件： -20℃

• 配置溶液浓度参考：
  

  	1mg	5mg	10mg
  1 mM	2.094 ml	10.472 ml	20.944 ml
  5 mM	0.419 ml	2.094 ml	4.189 ml
  10 mM	0.209 ml	1.047 ml	2.094 ml
  50 mM	0.042 ml	0.209 ml	0.419 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。

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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)

• pg ng μg mg g kg =
  fM pM nM μM mM M *
  nL μL mL L *