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1-[(1s)-1-(4-Chloro-3-Fluorophenyl)-2-Hydroxyethyl]-4-[2-(Tetrahydro-2h-Pyran-4-Ylamino)pyrimidin-4-Yl]pyridin-2(1h)-One

更新时间:2025-09-24 20:48:32

1-[(1s)-1-(4-Chloro-3-Fluorophenyl)-2-Hydroxyethyl]-4-[2-(Tetrahydro-2h-Pyran-4-Ylamino)pyrimidin-4-Yl]pyridin-2(1h)-One结构式
1-[(1s)-1-(4-Chloro-3-Fluorophenyl)-2-Hydroxyethyl]-4-[2-(Tetrahydro-2h-Pyran-4-Ylamino)pyrimidin-4-Yl]pyridin-2(1h)-One结构式
委托求购
常用名 1-[(1s)-1-(4-Chloro-3-Fluorophenyl)-2-Hydroxyethyl]-4-[2-(Tetrahydro-2h-Pyran-4-Ylamino)pyrimidin-4-Yl]pyridin-2(1h)-One 英文名 1-[(1s)-1-(4-Chloro-3-Fluorophenyl)-2-Hydroxyethyl]-4-[2-(Tetrahydro-2h-Pyran-4-Ylamino)pyrimidin-4-Yl]pyridin-2(1h)-One
CAS号 1453847-30-7 分子量 444.9
密度 N/A 沸点 N/A
分子式 C22H22ClFN4O3 熔点 N/A
MSDS N/A 闪点 N/A

 名称

英文名 1-[(1s)-1-(4-Chloro-3-Fluorophenyl)-2-Hydroxyethyl]-4-[2-(Tetrahydro-2h-Pyran-4-Ylamino)pyrimidin-4-Yl]pyridin-2(1h)-One

 物理化学性质

分子式 C22H22ClFN4O3
分子量 444.9
InChIKey PGGLRAWFUJMQBN-HXUWFJFHSA-N
SMILES O=c1cc(-c2ccnc(NC3CCOCC3)n2)ccn1C(CO)c1ccc(Cl)c(F)c1

 靶点实验

查看更多实验

实验名称:Inhibition of p90RSK phosphorylation in human HCT116 cells xenografted in nude mouse ...
来源:ChEMBL
靶标:HCT-116
External Id:CHEMBL3413973
实验名称:Antitumor activity against human HCT116 cells xenografted in nude mouse assessed as t...
来源:ChEMBL
靶标:NON-PROTEIN TARGET
External Id:CHEMBL3413974
实验名称:Inhibition of p90RSK phosphorylation in human HCT116 cells xenografted in nude mouse ...
来源:ChEMBL
靶标:HCT-116
External Id:CHEMBL3413972
实验名称:Inhibition of ERK1 (unknown origin) at 100 nM
来源:ChEMBL
靶标:Mitogen-activated protein kinase 3
External Id:CHEMBL3413977
实验名称:Inhibition of ERK2 (unknown origin) at 100 nM
来源:ChEMBL
靶标:Mitogen-activated protein kinase 1
External Id:CHEMBL3413978
实验名称:Toxicity in human HCT116 cells xenografted nude mouse assessed as body weight loss at...
来源:ChEMBL
靶标:Mus musculus
External Id:CHEMBL3413975
实验名称:Agonist activity at adenosine A1 receptor (unknown origin) at 10 uM
来源:ChEMBL
靶标:Adenosine receptor A1
External Id:CHEMBL3413979
实验名称:ERK-2 Enzymatic Assay from US Patent US9259470: "Serine/threonine kinase inhibitors"
来源:BindingDB
靶标:N/A
External Id:BindingDB_7622_1
实验名称:T>IC50 for inhibition of p90RSK phosphorylation in CD-1 mouse at 10 mg/kg, po
来源:ChEMBL
靶标:Mus musculus
External Id:CHEMBL4425959
实验名称:Thermodynamic solubility of the compound at pH 7.4
来源:ChEMBL
靶标:N/A
External Id:CHEMBL3412895
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