N-[4-(4-methylpiperazin-1-yl)phenyl]-6-phenylquinolin-4-amine

• 常用名: N-[4-(4-methylpiperazin-1-yl)phenyl]-6-phenylquinolin-4-amine
• 英文名: N-[4-(4-methylpiperazin-1-yl)phenyl]-6-phenylquinolin-4-amine
• CAS号: 144653-43-0
• 分子量: 394.51100
• 密度: N/A
• 沸点: N/A
• 分子式: C₂₆H₂₆N₄
• 熔点: N/A
• 闪点: N/A

名称

• 英文名: N-[4-(4-methylpiperazin-1-yl)phenyl]-6-phenylquinolin-4-amine

物理化学性质

• 分子式: C₂₆H₂₆N₄
• 分子量: 394.51100
• 精确质量: 394.21600
• PSA: 34.63000
• LogP: 4.82200
• InChIKey: YMBNETKULXIEPR-UHFFFAOYSA-N
• SMILES: CN1CCN(c2ccc(Nc3ccnc4ccc(-c5ccccc5)cc34)cc2)CC1

靶点实验

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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：Biochemical screen of P. falciparum CDPK1 来源：1187 靶标：Calcium-Dependent Protein Kinase 1 (CDPK1) External Id：PfalCDPK1

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：Biochemical screen of P. falciparum PK7 来源：1187 靶标：Protein Kinase 7 (PK7) External Id：PfalPK7

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：Biochemical screen of P. falciparum PK6 来源：1187 靶标：Protein Kinase 6 (PK6) External Id：PfalPK6

实验名称：Biochemical screen of P. falciparum MAPK2 来源：1187 靶标：mitogen-activated protein kinase 2 (MAP2 or MAPK2) External Id：PfalMAPK2

实验名称：Biochemical screen of P. falciparum CDPK4 来源：1187 靶标：Calcium-Dependent Protein Kinase 4 (CDPK4) External Id：PfalCDPK4

实验名称：Apparent permeability across human Caco-2 cells 来源：ChEMBL 靶标：Caco-2 External Id：CHEMBL1211550

实验名称：Inhibition of MK2 assessed as inhibition of [33P]ATP incorporation in to substrate af... 来源：ChEMBL 靶标：MAP kinase-activated protein kinase 2 External Id：CHEMBL1211491

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