N-(4-{[4-methyl-6-(pyrrolidin-1-yl)pyrimidin-2-yl]amino}phenyl)-2-phenoxypropanamide

• 常用名: N-(4-{[4-methyl-6-(pyrrolidin-1-yl)pyrimidin-2-yl]amino}phenyl)-2-phenoxypropanamide
• 英文名: N-(4-{[4-methyl-6-(pyrrolidin-1-yl)pyrimidin-2-yl]amino}phenyl)-2-phenoxypropanamide
• CAS号: 923132-46-1
• 分子量: 417.5
• 密度: N/A
• 沸点: N/A
• 分子式: C₂₄H₂₇N₅O₂
• 熔点: N/A
• 闪点: N/A

名称

• 英文名: N-(4-{[4-methyl-6-(pyrrolidin-1-yl)pyrimidin-2-yl]amino}phenyl)-2-phenoxypropanamide

物理化学性质

• 分子式: C₂₄H₂₇N₅O₂
• 分子量: 417.5
• InChIKey: HJYKBRIKCZGQLS-UHFFFAOYSA-N
• SMILES: Cc1cc(N2CCCC2)nc(Nc2ccc(NC(=O)C(C)Oc3ccccc3)cc2)n1

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：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：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

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