1-Imidazolidinecarboxamide, N-[4-[(6,7-dimethoxy-4-quinolinyl)oxy]-3-fluorophenyl]-2-oxo-3-phenyl

• 常用名: 1-Imidazolidinecarboxamide, N-[4-[(6,7-dimethoxy-4-quinolinyl)oxy]-3-fluorophenyl]-2-oxo-3-phenyl
• 英文名: 1-Imidazolidinecarboxamide, N-[4-[(6,7-dimethoxy-4-quinolinyl)oxy]-3-fluorophenyl]-2-oxo-3-phenyl
• CAS号: 1000850-34-9
• 分子量: 502.5
• 密度: N/A
• 沸点: N/A
• 分子式: C₂₇H₂₃FN₄O₅
• 熔点: N/A
• 闪点: N/A

名称

• 英文名: 1-Imidazolidinecarboxamide, N-[4-[(6,7-dimethoxy-4-quinolinyl)oxy]-3-fluorophenyl]-2-oxo-3-phenyl

物理化学性质

• 分子式: C₂₇H₂₃FN₄O₅
• 分子量: 502.5
• InChIKey: MCTIWUDXKBCHRY-UHFFFAOYSA-N
• SMILES: COC1=CC2=C(C=CN=C2C=C1OC)OC3=C(C=C(C=C3)NC(=O)N4CCN(C4=O)C5=CC=CC=C5)F

靶点实验

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实验名称：Inhibition Assay from Article 10.1155/2012/412614: "Identification of a Novel Series ... 来源：BindingDB 靶标：N/A External Id：BindingDB_5762_1

实验名称：Bioavailability in rat 来源：ChEMBL 靶标：Rattus norvegicus External Id：CHEMBL1047339

实验名称：Half life in rat 来源：ChEMBL 靶标：Rattus norvegicus External Id：CHEMBL1047338

实验名称：Inhibition of Aurora A at 100 uM 来源：ChEMBL 靶标：Aurora kinase A External Id：CHEMBL1047347

实验名称：Inhibition of CDK2/cyclin E at 100 uM 来源：ChEMBL 靶标：G1/S-specific cyclin-E2 External Id：CHEMBL1047348

实验名称：Antiangiogenic activity against HUVEC cell assessed as inhibition of VEGF-dependent t... 来源：ChEMBL 靶标：HUVEC External Id：CHEMBL1047345

实验名称：Inhibition of ALK at 100 uM 来源：ChEMBL 靶标：ALK tyrosine kinase receptor External Id：CHEMBL1047346

实验名称：Inhibition of FGFR1 at 100 uM 来源：ChEMBL 靶标：Fibroblast growth factor receptor 1 External Id：CHEMBL1047355

实验名称：Inhibition of Flt3 at 100 uM 来源：ChEMBL 靶标：Receptor-type tyrosine-protein kinase FLT3 External Id：CHEMBL1047356

实验名称：Inhibition of c-SRC at 100 uM 来源：ChEMBL 靶标：Proto-oncogene tyrosine-protein kinase Src External Id：CHEMBL1047353

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