Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4046 |
BX517
PDK1 inhibitor 2,BX 517,BX-517 |
Akt; PDK | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
BX517 (PDK1 inhibitor 2) 是一种选择性 PDK1抑制剂,其 IC50=6 nM。 | |||
T79723 |
PDK-IN-2
|
||
PDK-IN-2(Compound 1F)是一种具有IC50为68 nM的PDK抑制剂。该化合物能够抑制PDK1和PDK4在细胞内的表达,增强线粒体生物能并降低糖酵解表型,同时诱导细胞走向线粒体途径的apoptosis。此外,PDK-IN-2在4T1同基因小鼠模型中能够有效抑制肿瘤生长。 | |||
T38263 |
TBK1/IKKε-IN-4
TBK1/IKKε-IN-4 |
||
TBK1/IKKε-IN-4 is a 6-aminopyrazolopyrimidine derivative and a potent, selective TBK1 and IKKε inhibitor with IC50 values of 13 nM and 59 nM, respectively. TBK1/IKKε-IN-4 shows 100- to 1000-fold less activity against other protein kinases including PDK1, PI3K family members and mTOR[1]. TBK1/IKKε-IN-4 (Compound II; 96 hours; A549 andHCC44 cells) treatmentdisplays selective toxicity in TBK1-dependent cancer cell lines (IC50 of ~ 4.2 μM for H441 cells and IC50 of ~0.4 μM for A549 cells)[1].TBK1/IK... |