2-[(2,4-Difluorophenyl)amino]-7-[(2S)-2,3-dihydroxypropoxy]-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-one结构式
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常用名 | 2-[(2,4-Difluorophenyl)amino]-7-[(2S)-2,3-dihydroxypropoxy]-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-one | 英文名 | 2-[(2,4-Difluorophenyl)amino]-7-[(2S)-2,3-dihydroxypropoxy]-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-one |
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| CAS号 | 1221485-84-2 | 分子量 | 425.4 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C24H21F2NO4 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | 2-[(2,4-Difluorophenyl)amino]-7-[(2S)-2,3-dihydroxypropoxy]-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-one |
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| 分子式 | C24H21F2NO4 |
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| 分子量 | 425.4 |
| InChIKey | HXMGCTFLLWPVFM-SFHVURJKSA-N |
| SMILES | O=C1c2ccc(Nc3ccc(F)cc3F)cc2CCc2ccc(OCC(O)CO)cc21 |
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实验名称:Metabolic stability in human/rat liver microsomes at 1 mg/ml after 180 mins by LC/MS ...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL3090382
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实验名称:Inhibition of SRC at 10 uM
来源:ChEMBL
靶标:Proto-oncogene tyrosine-protein kinase Src
External Id:CHEMBL2155540
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实验名称:Inhibition of BRAF V600E mutant at 10 uM
来源:ChEMBL
靶标:Serine/threonine-protein kinase B-raf
External Id:CHEMBL2155541
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实验名称:Inhibition of TRKB at 10 uM
来源:ChEMBL
靶标:BDNF/NT-3 growth factors receptor
External Id:CHEMBL2155538
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实验名称:Competitive inhibition of p38alpha MAP kinase (unknown origin) in presence of 100 uM ...
来源:ChEMBL
靶标:Mitogen-activated protein kinase 14
External Id:CHEMBL3090387
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实验名称:Inhibition of p38alpha MAP kinase in human whole blood assessed as inhibition of LPS-...
来源:ChEMBL
靶标:Mitogen-activated protein kinase 14
External Id:CHEMBL3090388
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实验名称:Inhibition of p38alpha-dependent TNFalpha production in human whole blood
来源:ChEMBL
靶标:Mitogen-activated protein kinase 14
External Id:CHEMBL2155533
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实验名称:Inhibition of p38alpha by immunosorbent based kinase assay
来源:ChEMBL
靶标:Mitogen-activated protein kinase 14
External Id:CHEMBL2155531
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实验名称:Inhibition of SAK at 10 uM
来源:ChEMBL
靶标:Serine/threonine-protein kinase PLK4
External Id:CHEMBL2155536
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