CAS NO: | 702675-74-9 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
1 g | 电议 |
生物活性 | BX795 is a potent and selective inhibitor ofPDK1, with anIC50of 6 nM. BX795 is also a potent and relatively specific inhibitor ofTBK1andIKKe, with anIC50of 6 and 41 nM, respectively. BX795 blocks phosphorylation of S6K1,Akt,PKCδ, and GSK3β, and has lower selectivity overPKA,PKC,c-Kit, GSK3β etc. BX795 modulatesautophagy[1][2][3][4]. | ||||||||||||||||
IC50& Target[1][2] |
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体外研究 (In Vitro) | BX795 effectively blocks PDK1 activity in PC-3 cells, as shown by their ability to block phosphorylation of S6K1, Akt, PKCδ, and GSK3β. BX795 potently inhibits tumor cell growth on plastic with IC50of 1.6, 1.4, and 1.9 μM for MDA-468, HCT-116 and MiaPaca cells, respectively. In soft agar, BX795 displays higher growth inhibition with IC50of 0.72, and 0.25 μM for MDA-468, and PC-3 cells, respectively[1]. In addition, BX795, as an inhibitor of the TBK1/IKKε, blocks TBK1- and IKKε-mediated activation of IRF3 and production of IFN-β[2]. In platelet physiological responses, BX795 produces inhibitory effect on 2-MeSADP-induced or collagen-induced aggregation, ATP secretion and thromboxane generation[3]. | ||||||||||||||||
分子量 | 591.47 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C23H26IN7O2S | ||||||||||||||||
CAS 号 | 702675-74-9 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 33.33 mg/mL(56.35 mM;Need ultrasonic) 配制储备液
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以下溶剂前显示的百
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