5,6-二氢-5-氧代吲哚并[1,2-a]喹唑啉-7-乙酸结构式
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常用名 | 5,6-二氢-5-氧代吲哚并[1,2-a]喹唑啉-7-乙酸 | 英文名 | 5,6-Dihydro-5-oxoindolo[1,2-a]quinazoline-7-acetic acid |
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| CAS号 | 391670-48-7 | 分子量 | 292.29 | |
| 密度 | 1.46 | 沸点 | N/A | |
| 分子式 | C17H12N2O3 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
用途IQA (CGP-029482) 是一种有效的选择性蛋白激酶 CK2 抑制剂。 |
| 中文名 | 5,6-二氢-5-氧代吲哚并[1,2-a]喹唑啉-7-乙酸 |
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| 英文名 | (5-Oxo-5,6-dihydroindolo[1,2-a]quinazolin-7-yl)acetic acid |
| 描述 | IQA (CGP-029482) 是一种有效的选择性蛋白激酶 CK2 抑制剂。 |
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| 相关类别 | |
| 靶点实验 |
CK2 |
| 参考文献 |
| 密度 | 1.46 |
|---|---|
| 分子式 | C17H12N2O3 |
| 分子量 | 292.29 |
| 精确质量 | 292.08500 |
| PSA | 74.83000 |
| LogP | 2.97340 |
| InChIKey | INSBKYCYLCEBOD-UHFFFAOYSA-N |
| SMILES | O=C(O)Cc1c2ccccc2n2c1[nH]c(=O)c1ccccc12 |
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实验名称:Inhibition of Platelet derived growth factor receptor beta at 10 uM
来源:ChEMBL
靶标:Platelet-derived growth factor receptor beta
External Id:CHEMBL766059
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实验名称:Inhibition of Protein kinase B at 10 uM
来源:ChEMBL
靶标:RAC-alpha serine/threonine-protein kinase
External Id:CHEMBL766861
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实验名称:Inhibition of CK2 (unknown origin)
来源:ChEMBL
靶标:Casein kinase II subunit alpha 3
External Id:CHEMBL5382176
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实验名称:Experimentally measured binding affinity data (Ki) for protein-ligand complexes deriv...
来源:Shanghai Institute of Organic Chemistry
靶标:N/A
External Id:PDBbind-Ki for protein-ligand complexes
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实验名称:Inhibition of Protein kinase Raf-1 at 10 uM
来源:ChEMBL
靶标:RAF proto-oncogene serine/threonine-protein kinase
External Id:CHEMBL769164
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实验名称:Binding affinity to CK2 (unknown origin) assessed as inhibition constant
来源:ChEMBL
靶标:Casein kinase II subunit alpha 3
External Id:CHEMBL5382174
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实验名称:Inhibition of Protein kinase Src at 10 uM
来源:ChEMBL
靶标:Proto-oncogene tyrosine-protein kinase Src
External Id:CHEMBL772797
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实验名称:Inhibition of Protein kinase fibroblast growth factor receptor 1 at 10 uM
来源:ChEMBL
靶标:Fibroblast growth factor receptor 1
External Id:CHEMBL772801
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实验名称:Percent residual JNK activity in the presence of 10uM inhibitor
来源:ChEMBL
靶标:Mitogen-activated protein kinase 9
External Id:CHEMBL1061151
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