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2-[(2,4-Difluorophenyl)amino]-7-[(2S)-2,3-dihydroxypropoxy]-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-one

更新时间:2025-11-03 17:06:18

2-[(2,4-Difluorophenyl)amino]-7-[(2S)-2,3-dihydroxypropoxy]-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-one结构式
2-[(2,4-Difluorophenyl)amino]-7-[(2S)-2,3-dihydroxypropoxy]-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-one结构式
委托求购
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
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

 名称

英文名 2-[(2,4-Difluorophenyl)amino]-7-[(2S)-2,3-dihydroxypropoxy]-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-one

 物理化学性质

分子式 C24H21F2NO4
分子量 425.4
InChIKey HXMGCTFLLWPVFM-SFHVURJKSA-N
SMILES O=C1c2ccc(Nc3ccc(F)cc3F)cc2CCc2ccc(OCC(O)CO)cc21

 靶点实验

查看更多实验

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
实验名称:Inhibition of SRC at 10 uM
来源:ChEMBL
靶标:Proto-oncogene tyrosine-protein kinase Src
External Id:CHEMBL2155540
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
实验名称:Inhibition of TRKB at 10 uM
来源:ChEMBL
靶标:BDNF/NT-3 growth factors receptor
External Id:CHEMBL2155538
实验名称:Inhibition of AuroraB at 10 uM
来源:ChEMBL
靶标:Aurora kinase B
External Id:CHEMBL2155539
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
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
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
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
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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