Chemical Structure : PF-7006
货号: PC-21557Not For Human Use, Lab Use Only.
PF-7006 is a potent, highly-selective Mps1 (TTK) inhibitor with Ki of 0.27 nM, potently inhibit Mps1 in MDA-MB-468 tumor cells with IC50 of 2.5 nM.
大包装,大折扣!
E-mail: sales@probechem.com
Tech Support: tech@probechem.com
PF-7006 is a potent, highly-selective Mps1 (TTK) inhibitor with Ki of 0.27 nM, potently inhibit Mps1 in MDA-MB-468 tumor cells with IC50 of 2.5 nM.
PF-7006 triggers signaling events consistent with mitotic checkpoint abrogation.
PF-7006 at 25 mg/kg inhibited tuomor growth in the HCC1806 triple-negative breast cancer model.
PF-7006 inhibitor-induced cytotoxicity as function of retinoblastoma tumor suppressor protein (Rb1) status in tHMEC cultures co-treated with the CDK4/6 inhibitor palabociclib.
PF-7006 is shown to be selectively cytotoxic to Rb1-deficient cells relative to Rb1-competent cells.
分子量 | 434.50 | |
分子式 | C22H26N8O2 | |
外观性状 | Solid | |
储存条件 |
|
|
Solubility |
10 mM in DMSO |
1. Ricardo Martinez, et al. PLoS One. 2015 Sep 23;10(9):e0138616.
备案号:沪ICP备16042516号-1 Copyright © 2022 probechem.com. All Rights Reserved. probechem Copyright