6-(5-(2,4-difluorophenylsulfonamido)-6-methoxypyridin-3-yl)-N-(2-morpholino ethyl)imidazo[1,2-a]pyridine-3-carboxamide

• 常用名: 6-(5-(2,4-difluorophenylsulfonamido)-6-methoxypyridin-3-yl)-N-(2-morpholino ethyl)imidazo[1,2-a]pyridine-3-carboxamide
• 英文名: 6-(5-(2,4-difluorophenylsulfonamido)-6-methoxypyridin-3-yl)-N-(2-morpholino ethyl)imidazo[1,2-a]pyridine-3-carboxamide
• CAS号: 2125500-60-7
• 分子量: 572.6
• 密度: N/A
• 沸点: N/A
• 分子式: C₂₆H₂₆F₂N₆O₅S
• 熔点: N/A
• 闪点: N/A

名称

• 英文名: 6-(5-(2,4-difluorophenylsulfonamido)-6-methoxypyridin-3-yl)-N-(2-morpholino ethyl)imidazo[1,2-a]pyridine-3-carboxamide

物理化学性质

• 分子式: C₂₆H₂₆F₂N₆O₅S
• 分子量: 572.6
• InChIKey: AOFNYCXYCYLTJD-UHFFFAOYSA-N
• SMILES: COC1=C(C=C(C=N1)C2=CN3C(=NC=C3C(=O)NCCN4CCOCC4)C=C2)NS(=O)(=O)C5=C(C=C(C=C5)F)F

靶点实验

查看更多实验

实验名称：Antiproliferative activity against human HCT116 cells after 72 hrs by SRB assay 来源：ChEMBL 靶标：HCT-116 External Id：CHEMBL4193525

实验名称：Antiproliferative activity against human HT-29 cells assessed as inhibition of cell g... 来源：ChEMBL 靶标：HT-29 External Id：CHEMBL5356227

实验名称：Antiproliferative activity against human MDA-MB-231 cells after 72 hrs by SRB assay 来源：ChEMBL 靶标：MDA-MB-231 External Id：CHEMBL4193527

实验名称：Antiproliferative activity against human SKHEP1 cells after 72 hrs by SRB assay 来源：ChEMBL 靶标：SK-HEP1 External Id：CHEMBL4193526

实验名称：Inhibition of PI3Kalpha (unknown origin) using PIP2 as substrate incubated for 1 hr i... 来源：ChEMBL 靶标：Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform External Id：CHEMBL5356226

实验名称：Selectivity ratio of IC50 for HUVEC to IC50 for human HCT116 cells 来源：ChEMBL 靶标：N/A External Id：CHEMBL4193533

实验名称：Selectivity ratio of IC50 for HUVEC to IC50 for human MDA-MB-231 cells 来源：ChEMBL 靶标：N/A External Id：CHEMBL4193534

实验名称：Antiproliferative activity against human A549 cells after 72 hrs by SRB assay 来源：ChEMBL 靶标：A549 External Id：CHEMBL4193529

实验名称：Antiproliferative activity against human SNU638 cells after 72 hrs by SRB assay 来源：ChEMBL 靶标：SNU-638 External Id：CHEMBL4193528

实验名称：Inhibition of PI3K in human HCT116 cells assessed as reduction in Akt phosphorylation... 来源：ChEMBL 靶标：N/A External Id：CHEMBL4193531

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