当前位置:产品>信号通路产品>抑制剂>产品详情

WAY-600
Catalog Number: E1KS2689
Amount: 5mg1​ PHYSICAL AND CHEMICAL PROPERTIES
Applications: Reactivity:
产品类型: Unconjugated
发货周期: 现货
说明书:     PDF
总价格:    816元
选择数量:

-
+

咨询客服
概述
  • Catalog Number:

    E1KS2689
  • Amount:

    5mg1​ PHYSICAL AND CHEMICAL PROPERTIES

2​ Biological Activity
WAY-600 is a potent ATP-competitive mTOR inhibitor with an IC50 of about 9 nM. It is well reported that the mammalian target of rapamycin (mTOR) is centrally involved in cell growth, metabolism, and angiogenesis. WAY-600 has significant selectivity against mTOR over phosphatidylinositol 3-kinase (PI3K) isofoms (>100-fold). WAY-600 treated HEK293 cells indicated a 50% inhibition of polysomes by way-600 compared with the 11% suppression by rapamycin. Unlike the rapalogs,WAY-600 acutely blocked mTORC2-dependent phosphorylation of AKT in vitro and in vivo. In various cancer cells,WAY-600 inhibited the mTORC1 substrate P-S6K(T389) and mTORC2 substrate P-AKT(S473) at submicromolar concentrations without significant inhibition of P-AKT(T308). [1][2]
3​ References:
Biochemical, cellular, and in vivo activity of novel ATP-competitive and selective inhibitors of the mammalian target of rapamycin Yu K et al. Cancer Res 2009 Aug 1;69(15):6232-40
mTOR Mediated Anti-Cancer Drug Discovery. Liu Q et al. Drug Discov Today Ther Strateg 2009;6(2):47-55
The pharmacological and toxicological properties of this product have not been fully investigated. Exercise caution in use and handling. This product must not be used in humans.

2​ Biological Activity WAY-600 is a potent ATP-competitive mTOR inhibitor with an IC50 of about 9 nM. It is well reported that the mammalian target of rapamycin (mTOR) is centrally involved in cell growth, metabolism, and angiogenesis. WAY-600 has significant selectivity against mTOR over phosphatidylinositol 3-kinase (PI3K) isofoms (>100-fold). WAY-600 treated HEK293 cells indicated a 50% inhibition of polysomes by way-600 compared with the 11% suppression by rapamycin. Unlike the rapalogs,WAY-600 acutely blocked mTORC2-dependent phosphorylation of AKT in vitro and in vivo. In various cancer cells,WAY-600 inhibited the mTORC1 substrate P-S6K(T389) and mTORC2 substrate P-AKT(S473) at submicromolar concentrations without significant inhibition of P-AKT(T308). [1][2] 3​ References: Biochemical, cellular, and in vivo activity of novel ATP-competitive and selective inhibitors of the mammalian target of rapamycin Yu K et al. Cancer Res 2009 Aug 1;69(15):6232-40 mTOR Mediated Anti-Cancer Drug Discovery. Liu Q et al. Drug Discov Today Ther Strateg 2009;6(2):47-55 The pharmacological and toxicological properties of this product have not been fully investigated. Exercise caution in use and handling. This product must not be used in humans.

相关推荐

Responsive image
Catalog Number:E1KS2150
Amount:5mg
Reactivity:
Applications:    
Swiss-Prot No.
Price:816元
Responsive image
Catalog Number:E1KS1153
Amount:10mg
Reactivity:
Applications:    
Swiss-Prot No.
Price:816元
Responsive image
SP600125   
Catalog Number:E1KS1460
Amount:50mg
Reactivity:
Applications:    
Swiss-Prot No.
Price:816元