1-(4-Tert-butylphenyl)-3-(3-(6,7-dimethoxyquinazolin-4-yloxy)phenyl)urea结构式
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常用名 | 1-(4-Tert-butylphenyl)-3-(3-(6,7-dimethoxyquinazolin-4-yloxy)phenyl)urea | 英文名 | 1-(4-Tert-butylphenyl)-3-(3-(6,7-dimethoxyquinazolin-4-yloxy)phenyl)urea |
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| CAS号 | 1188909-76-3 | 分子量 | 472.5 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C27H28N4O4 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | 1-(4-Tert-butylphenyl)-3-(3-(6,7-dimethoxyquinazolin-4-yloxy)phenyl)urea |
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| 分子式 | C27H28N4O4 |
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| 分子量 | 472.5 |
| InChIKey | BWKRBEKNGFHQLO-UHFFFAOYSA-N |
| SMILES | CC(C)(C)C1=CC=C(C=C1)NC(=O)NC2=CC(=CC=C2)OC3=NC=NC4=CC(=C(C=C43)OC)OC |
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实验名称:Inhibition of BRAF V600E mutant-dependent MEK phosphorylation in A375 cells
来源:ChEMBL
靶标:Serine/threonine-protein kinase B-raf
External Id:CHEMBL1828156
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实验名称:Cytotoxicity against human A375 cells expressing BRAF V600E mutant after 72 hrs by ce...
来源:ChEMBL
靶标:A-375
External Id:CHEMBL2033393
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实验名称:Competition Binding Assay from US Patent US9730937: "RAF kinase modulator compounds a...
来源:BindingDB
靶标:N/A
External Id:BindingDB_1637_1
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实验名称:Inhibition of BRAF V600E mutant in human HEK293 cells after 1 hr by competition bindi...
来源:ChEMBL
靶标:Serine/threonine-protein kinase B-raf
External Id:CHEMBL2033391
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实验名称:Inhibition of BRAF V600E mutant-mediated MEK phosphorylation in human A375 cells afte...
来源:ChEMBL
靶标:Serine/threonine-protein kinase B-raf
External Id:CHEMBL2033392
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实验名称:Binding affinity to BRAF V600E mutant
来源:ChEMBL
靶标:Serine/threonine-protein kinase B-raf
External Id:CHEMBL1828155
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