1188296-52-7
中文名称
无中文名称
英文名称
PF 4800567 hydrochloride
CAS
1188296-52-7
分子式
C17H18ClN5O2
分子量
359.81
MOL 文件
1188296-52-7.mol
更新日期
2026/01/27 15:55:09
1188296-52-7 结构式
基本信息
中文别名
化合物PF-4800567PF-4800567游离态
3-[(3-氯苯氧基)甲基]-1-(四氢-2H-吡喃-4-基)-1H-吡唑并[3,4-D]嘧啶-4-胺
英文别名
PF 4800567PF 4800567
PF-4800567
PF 4800567 hydrochloride
3-[(3-chlorophenoxy)methyl]-1-(oxan-4-yl)pyrazolo[3,4-d]pyrimidin-4-amine
3-[(3-Chlorophenoxy)methyl]-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
1H-Pyrazolo[3,4-d]pyrimidin-4-amine, 3-[(3-chlorophenoxy)methyl]-1-(tetrahydro-2H-pyran-4-yl)-
3-[(3-Chlorophenoxy)Methyl]-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-d]pyriMidin-4-aMine Hydrochloride
所属类别
生物:小分子化合物物理化学性质
沸点592.9±50.0 °C(Predicted)
密度1.52±0.1 g/cm3(Predicted)
储存条件Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
溶解度DMF: 25 mg/ml; DMF:PBS(pH 7.2)(1:1): 0.5 mg/ml; DMSO: 10 mg/ml; Ethanol: 1 mg/ml
酸度系数(pKa)4.01±0.30(Predicted)
形态结晶固体
颜色Light yellow to yellow
InChI1S/C17H18ClN5O2/c18-11-2-1-3-13(8-11)25-9-14-15-16(19)20-10-21-17(15)23(22-14)12-4-6-24-7-5-12/h1-3,8,10,12H,4-7,9H2,(H2,19,20,21)
InChIKeyAUMDBEHGJRZSOO-UHFFFAOYSA-N
SMILESNC1=NC=NC2=C1C(COC3=CC=CC(Cl)=C3)=NN2C4CCOCC4
应用领域
用途1
PF 4800567 is a selective casein kinase 1蔚 inhibitor; displays 22-fold greater potency towards CK1蔚 than CK1δ (IC50 values are 32 and 711 nM for CK1蔚 and CK1δ respectively). ATP competitive. Displays
minimal effect on the circadian clock.PF 4800567价格(试剂级)
| 报价日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
| 2025/12/22 | HY-12470 | PF-4800567 | 1188296-52-7 | 1 mg | 192元 |
| 2025/12/22 | HY-12470 | 3-((3-氯苯氧基)甲基)-1-(四氢-2H-吡喃-4-基)-1H-吡唑并[3,4-D]嘧啶-4-胺 PF-4800567 | 1188296-52-7 | 5mg | 477元 |
| 2025/12/22 | HY-12470 | 3-((3-氯苯氧基)甲基)-1-(四氢-2H-吡喃-4-基)-1H-吡唑并[3,4-D]嘧啶-4-胺 PF-4800567 | 1188296-52-7 | 10mg | 777元 |
常见问题列表
生物活性
PF 4800567是casein kinase 1 epsilon (IC50=32 nM) 的新型有效抑制剂,其选择性是casein kinase 1 delta(IC50=711 nM)的20倍以上。靶点
| Target | Value |
|
casein kinase 1 epsilon
(Cell-free assay) | 32 nM |
|
casein kinase 1 delta
() | 711 nM |
体外研究
PF-4800567 is a potent and selective inhibitor of casein kinase 1ϵ (CK1ϵ), with an IC 50 of 32 nM, which is greater than 20-fold selectivity over CK1δ (IC 50 , 711 nM). PF-4800567 shows inhibitory activity against CK1ϵ and CK1δ in whole cells, with IC 50 s of 2.65 and 20.38 μM, respectively. PF-4800567 (0.01-10 μM) blocks CK1ϵ-mediated PER3 nuclear localization mediated by CK1ϵ and suppresses PER2 degradation at 1 μM. In addition, PF-4800567 has little effect on the circadian clock at 32 nM.
体内研究
PF-4800567 (100 mg/kg, s.c.) is rapidly absorpted and distributed in plasma and brain of mice.
