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N-(4-{[4-(dimethylamino)-6-methylpyrimidin-2-yl]amino}phenyl)-3,5-dimethoxybenzamide

更新时间:2025-08-29 18:28:16

N-(4-{[4-(dimethylamino)-6-methylpyrimidin-2-yl]amino}phenyl)-3,5-dimethoxybenzamide结构式
N-(4-{[4-(dimethylamino)-6-methylpyrimidin-2-yl]amino}phenyl)-3,5-dimethoxybenzamide结构式
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常用名 N-(4-{[4-(dimethylamino)-6-methylpyrimidin-2-yl]amino}phenyl)-3,5-dimethoxybenzamide 英文名 N-(4-{[4-(dimethylamino)-6-methylpyrimidin-2-yl]amino}phenyl)-3,5-dimethoxybenzamide
CAS号 946368-92-9 分子量 407.5
密度 N/A 沸点 N/A
分子式 C22H25N5O3 熔点 N/A
MSDS N/A 闪点 N/A

 名称

英文名 N-(4-{[4-(dimethylamino)-6-methylpyrimidin-2-yl]amino}phenyl)-3,5-dimethoxybenzamide

 物理化学性质

分子式 C22H25N5O3
分子量 407.5
InChIKey WQRUTHPPWJRWRB-UHFFFAOYSA-N
SMILES COc1cc(OC)cc(C(=O)Nc2ccc(Nc3nc(C)cc(N(C)C)n3)cc2)c1

 靶点实验

查看更多实验

实验名称:ST_JUDE_LEISH: Cytotoxicity at 2uM final concentration against transgenic Leishmania ...
来源:ChEMBL
靶标:Glucose transporter
External Id:CHEMBL3436044
实验名称:Heme synthesis enzyme ferrochelatase (FECH) inhibition: small molecule primary screen
来源:24913
靶标:N/A
External Id:FECH 20K screen
实验名称:Inhibition of Trypanosoma cruzi CYP51
来源:ChEMBL
靶标:Sterol 14-alpha demethylase
External Id:CHEMBL4235946
实验名称:ST_JUDE_LEISH: Cytotoxicity at 2uM final concentration against transgenic Leishmania ...
来源:ChEMBL
靶标:Solute carrier family 2, facilitated glucose transporter member 1
External Id:CHEMBL3436042
实验名称:ST_JUDE_LEISH: Cytotoxicity at 2uM final concentration against transgenic Leishmania ...
来源:ChEMBL
靶标:Hexose transporter 1
External Id:CHEMBL3436043
实验名称:Selectivity ratio of pEC50 for African green monkey Vero cells to pEC50 for Trypanoso...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL4235943
实验名称:Cytotoxicity against African green monkey Vero cells
来源:ChEMBL
靶标:Vero
External Id:CHEMBL4235942
实验名称:Intrinsic clearance in CD-1 mouse liver microsomes at 0.5 uM after 30 mins in presenc...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL4235945
实验名称:Kinetic solubility of the compound in water up to 250 uM by laser nephelometry
来源:ChEMBL
靶标:N/A
External Id:CHEMBL4235944
实验名称:Small-molecule inhibitors of ST2 (IL1RL1)
来源:20881
靶标:interleukin-1 receptor-like 1 isoform [homo sapiens]
External Id:ST2_IL33_Inhibitors_Primary_Screening_77700
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