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4-Chloro-5-(2,6-di-4-morpholinyl-4-pyrimidinyl)-2-pyridinamine

更新时间:2025-10-07 14:56:07

4-Chloro-5-(2,6-di-4-morpholinyl-4-pyrimidinyl)-2-pyridinamine结构式
4-Chloro-5-(2,6-di-4-morpholinyl-4-pyrimidinyl)-2-pyridinamine结构式
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常用名 4-Chloro-5-(2,6-di-4-morpholinyl-4-pyrimidinyl)-2-pyridinamine 英文名 4-Chloro-5-(2,6-di-4-morpholinyl-4-pyrimidinyl)-2-pyridinamine
CAS号 944397-11-9 分子量 376.8
密度 N/A 沸点 N/A
分子式 C17H21ClN6O2 熔点 N/A
MSDS N/A 闪点 N/A

 名称

英文名 4-Chloro-5-(2,6-di-4-morpholinyl-4-pyrimidinyl)-2-pyridinamine

 物理化学性质

分子式 C17H21ClN6O2
分子量 376.8
InChIKey JKVGJGBIUVYAIV-UHFFFAOYSA-N
SMILES Nc1cc(Cl)c(-c2cc(N3CCOCC3)nc(N3CCOCC3)n2)cn1

 靶点实验

查看更多实验

实验名称:Oral bioavailability in rat at 20 mg/kg
来源:ChEMBL
靶标:Rattus norvegicus
External Id:CHEMBL2020163
实验名称:Intrinsic clearance in rat liver microsomes
来源:ChEMBL
靶标:Liver microsomes
External Id:CHEMBL2020167
实验名称:Intrinsic clearance in human liver microsomes
来源:ChEMBL
靶标:Liver microsomes
External Id:CHEMBL2020168
实验名称:Solubility of the compound at pH 7
来源:ChEMBL
靶标:N/A
External Id:CHEMBL2020166
实验名称:Antiproliferative activity against human A2780 cells after 3 days by CellTiter-Glo as...
来源:ChEMBL
靶标:A2780
External Id:CHEMBL2020155
实验名称:Inhibition of PI3K-mediated AKT Ser473 phosphorylation in human A2780 cells after 1 h...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL2020156
实验名称:Inhibition of PI3Kalpha using 1-alpha-phosphatidylinositol as substrate by ATP deplet...
来源:ChEMBL
靶标:Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
External Id:CHEMBL2020154
实验名称:Volume of distribution at steady state in rat at 5 mg/kg, iv
来源:ChEMBL
靶标:Rattus norvegicus
External Id:CHEMBL2020159
实验名称:Clearance in rat at 5 mg/kg, iv
来源:ChEMBL
靶标:Rattus norvegicus
External Id:CHEMBL2020157
实验名称:AUC in rat at 20 mg/kg, po
来源:ChEMBL
靶标:Rattus norvegicus
External Id:CHEMBL2020158
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