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首页-小分子抑制剂&激动剂-Cell Cycle/DNA Damage-Monopolar Spindle 1 (Mps1/TTK)-PF-7006
PF-7006

Chemical Structure : PF-7006

CAS No.: 2771955-09-8

PF-7006 (PF7006)

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.

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纯度 & COA & 质检文件 纯度: >98% (HPLC)

生物&药学活性

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.

物理化学性质&存储条件

分子量 434.50
分子式 C22H26N8O2
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

2-((2-methyl-6-morpholinopyridin-3-yl)amino)-4-((tetrahydro-2H-pyran-4-yl)amino)-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile

参考文献

1. Ricardo Martinez, et al. PLoS One. 2015 Sep 23;10(9):e0138616.

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