5-[(Z)-[6-[(2-fluoro-4-methoxybenzoyl)carbamoylamino]-2-oxo-1H-indol-3-ylidene]methyl]-2,4-dimethyl-N-(2-pyrrolidin-1-ylethyl)-1H-pyrrole-3-carboxamide

• 常用名: 5-[(Z)-[6-[(2-fluoro-4-methoxybenzoyl)carbamoylamino]-2-oxo-1H-indol-3-ylidene]methyl]-2,4-dimethyl-N-(2-pyrrolidin-1-ylethyl)-1H-pyrrole-3-carboxamide
• 英文名: 5-[(Z)-[6-[(2-fluoro-4-methoxybenzoyl)carbamoylamino]-2-oxo-1H-indol-3-ylidene]methyl]-2,4-dimethyl-N-(2-pyrrolidin-1-ylethyl)-1H-pyrrole-3-carboxamide
• CAS号: 1474049-64-3
• 分子量: 588.6
• 密度: N/A
• 沸点: N/A
• 分子式: C₃₁H₃₃FN₆O₅
• 熔点: N/A
• 闪点: N/A

名称

• 英文名: 5-[(Z)-[6-[(2-fluoro-4-methoxybenzoyl)carbamoylamino]-2-oxo-1H-indol-3-ylidene]methyl]-2,4-dimethyl-N-(2-pyrrolidin-1-ylethyl)-1H-pyrrole-3-carboxamide

物理化学性质

• 分子式: C₃₁H₃₃FN₆O₅
• 分子量: 588.6
• InChIKey: NKKNQMFHKZEGQU-KQWNVCNZSA-N
• SMILES: COc1ccc(C(=O)NC(=O)Nc2ccc3c(c2)NC(=O)C3=Cc2[nH]c(C)c(C(=O)NCCN3CCCC3)c2C)c(F)c1

靶点实验

查看更多实验

实验名称：Inhibition of FLT3-ITD mutant (unknown origin) 来源：ChEMBL 靶标：Receptor-type tyrosine-protein kinase FLT3 External Id：CHEMBL5230502

实验名称：Inhibition of FLT3 (unknown origin) using EAIYAAPFAKKK substrate 来源：ChEMBL 靶标：Receptor-type tyrosine-protein kinase FLT3 External Id：CHEMBL3380434

实验名称：Inhibition of AKT1 (unknown origin) at 1 uM 来源：ChEMBL 靶标：RAC-alpha serine/threonine-protein kinase External Id：CHEMBL3380431

实验名称：Inhibition of ABL1 (unknown origin) at 1 uM 来源：ChEMBL 靶标：Tyrosine-protein kinase ABL1 External Id：CHEMBL3380432

实验名称：Cytotoxicity against human THP1 cells assessed as cell viability after 48 hrs by MTT ... 来源：ChEMBL 靶标：THP-1 External Id：CHEMBL3380437

实验名称：Cytotoxicity against human HL60 cells assessed as cell viability after 48 hrs by MTT ... 来源：ChEMBL 靶标：NON-PROTEIN TARGET External Id：CHEMBL3380438

实验名称：Cytotoxicity against human MV4-11 cells assessed as cell viability after 48 hrs by MT... 来源：ChEMBL 靶标：MV4-11 External Id：CHEMBL3380435

实验名称：Cytotoxicity against human MOLM13 cells assessed as cell viability after 48 hrs by MT... 来源：ChEMBL 靶标：MOLM-13 External Id：CHEMBL3380436

实验名称：Permeability coefficient of the compound at pH 7.4 by PAMPA-GIT assay 来源：ChEMBL 靶标：N/A External Id：CHEMBL3380445

实验名称：Inhibition of Aurora A (unknown origin) at 1 uM 来源：ChEMBL 靶标：Aurora kinase A External Id：CHEMBL3380446

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