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BX-320
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
BX-320图片
规格:98%
分子量:547.5
包装与价格:
包装价格(元)
500ug询价
1mg询价
5mg询价

BX-320 是一种选择性的、ATP 竞争性的、口服活性的直接 PDK1 抑制剂,在直接激酶测定中其 IC50 为 30 nM。 BX-320 还诱导细胞凋亡。抗癌作用。
货号:ajcx24034
CAS:702676-93-5
分子式:C23H31BrN8O3
分子量:547.5
溶解度:DMSO: soluble
纯度:98%
存储:Store at -20°C
库存:现货

Background:

BX-320 is an inhibitor of the serine/threonine kinase 3-phosphoinositide-dependent protein kinase 1 (PDK1; IC50= 30 nM).1It is selective for PDK1 over a panel of 10 additional kinases (IC50s = >820 nM for all). BX-320 inhibits Akt and p70S6K1 phosphorylation in PC3 cells (IC50s = 1-3 µM). It induces apoptosis in, and inhibits the growth of, MDA-MB-468 breast cancer cells (IC50s = 0.5 and 0.6 µM, respectively), as well as inhibits cell growth in a panel of cancer cells (IC50s = 0.12-1.2 µM). BX-320 (200 mg/kg) inhibits the growth of lung tumors in a LOX melanoma mouse model of blood-borne metastasis.


1.Feldman, R.I., Wu, J.M., Polokoff, M.A., et al.Novel small molecule inhibitors of 3-phosphoinositide-dependent kinase-1J. Biol. Chem.280(20)19867-19874(2005)

 
 
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