2,3-Dimethyl-4-[[1-(1-oxo-2-propyn-1-yl)-4-piperidinyl]amino]-1H-indole-7-carboxamide结构式
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常用名 | 2,3-Dimethyl-4-[[1-(1-oxo-2-propyn-1-yl)-4-piperidinyl]amino]-1H-indole-7-carboxamide | 英文名 | 2,3-Dimethyl-4-[[1-(1-oxo-2-propyn-1-yl)-4-piperidinyl]amino]-1H-indole-7-carboxamide |
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| CAS号 | 1912444-66-6 | 分子量 | 338.4 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C19H22N4O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | 2,3-Dimethyl-4-[[1-(1-oxo-2-propyn-1-yl)-4-piperidinyl]amino]-1H-indole-7-carboxamide |
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| 分子式 | C19H22N4O2 |
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| 分子量 | 338.4 |
| InChIKey | RRVWOHOZIVWEIW-UHFFFAOYSA-N |
| SMILES | C#CC(=O)N1CCC(Nc2ccc(C(N)=O)c3[nH]c(C)c(C)c23)CC1 |
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实验名称:Enzyme Assay from US Patent US9920031: "Indole carboxamide compounds"
来源:BindingDB
靶标:N/A
External Id:BindingDB_2711_1
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实验名称:Inhibition of BTK in human Ramos B cells assessed as reduction in BCR-stimulated calc...
来源:ChEMBL
靶标:Tyrosine-protein kinase BTK
External Id:CHEMBL4616765
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实验名称:Inhibition of recombinant human BTK using fluoresceinated peptide as substrate after ...
来源:ChEMBL
靶标:Tyrosine-protein kinase BTK
External Id:CHEMBL4616764
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实验名称:Enzyme Assay from US Patent US10604504: "Indole carboxamide compounds"
来源:BindingDB
靶标:N/A
External Id:BindingDB_9073_1
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实验名称:Enzyme Assay from US Patent US9802915: "Indole carboxamide compounds"
来源:BindingDB
靶标:N/A
External Id:BindingDB_2079_1
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实验名称:Biological Assay from US Patent US11623921: "Indole carboxamide compounds"
来源:BindingDB
靶标:N/A
External Id:BindingDB_11202_1
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