For research use only. Not for therapeutic Use.
<p style=/line-height:25px/>ILK-IN-1 is a novel ILK inhibitor with IC50 of 0.6 μM.<br>IC50 value: 0.6 μM<br>Target: ILK<br>in vitro: ILK-IN-1 exhibits high potency against a panel of prostate and breast cancer cell lines (IC50, 1-2.5 μM). ILK-IN-1 facilitates the dephosphorylation of Akt at Ser-473 and other ILK targets, including glycogen synthase kinase-3β and myosin light chain. ILK-IN-1 suppresses the expression of the transcription/translation factor YB-1 and its targets HER2 and EGFR in PC-3 cells, which could be rescued by the stable expression of constitutively active ILK. ILK-IN-1 induces autophagy and apoptosis, both of which are integral to its antiproliferative activity.<br>in vivo: ILK-IN-1 is a single oral agent in suppressing PC-3 xenograft tumor growth.</p>
Catalog Number | I001269 |
CAS Number | 1333146-24-9 |
Molecular Formula | C30H30F3N5O |
Purity | ≥95% |
Target | Integrin |
Solubility | 10 mM in DMSO |
Storage | -20°C |
IC50 | 0.6 μM |
Reference | <p style=/line-height:25px/> </p> |