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爱思益普已建立了400+激酶
我们的优势：
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激酶种类多：目前已建成激酶库超过400个并不断扩大，覆盖常用酪氨酸激酶及常见突变激酶；
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检测准确：对于已有明确特异抑制剂的激酶选用其特异性抑制剂建立试验模型，控制IC50差异与文献报道值在5倍以内，最大不超过七倍；
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检测周期短：化合物检测出报告周期3-5个工作日，1-2个工作日可提交数据；
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检测方法：TR-FRET(LANCE Ultra, LhaScreen, HTRF)，荧光法(Kinase-Glo, ADP-Glo)，Z`-LYTE，Binding assay等。
爱思益普已建立的激酶列表
部分验证数据（需要更多验证数据请联系我们）
参考文献：
[1]. SNS-032 is a potent and selective CDK 2, 7 and 9 inhibitor th drives target modulion in pient samples. Cancer Chemother Pharmacol. 2009 Sep;64(4):723-32.
[2]. Preclinical characterizion of GLPG0634, a selective inhibitor of JAK1, for the trement of inflammory diseases. J Immunol. 2013, 191(7), 3568-3577.
[3].Optimizion of imidazo[4,5-b]pyridine-based kinase inhibitors: identificion of a dual FLT3/Aurora kinase inhibitor as an orally bioailable preclinical development candide for the trement of acute myeloid leukemia. J Med Chem. 2012 Oct 25;55(20):8721-34.
[4]. Specific inhibition of cyclin-dependent kinase 4/6 by PD 0332991 and associed antitumor activity in human tumor xenografts. Mol Cancer Ther. 2004 Nov;3(11):1427-38.
[5]. Peng SB, et al. Kinetic characterizion of novel pyrazole TGF-beta receptor I kinase inhibitors and their blockade of the epithelial-mesenchymal transition. Biochemistry, 2005, 44(7), 2293-2304.
