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6,8-Dibromo-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one

更新时间:2026-03-26 16:45:23

6,8-Dibromo-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one结构式
6,8-Dibromo-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one结构式
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常用名 6,8-Dibromo-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one 英文名 6,8-Dibromo-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one
CAS号 780778-55-4 分子量 426.05
密度 N/A 沸点 N/A
分子式 C16H10Br2O4 熔点 N/A
MSDS N/A 闪点 N/A

 名称

英文名 6,8-Dibromo-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one

 物理化学性质

分子式 C16H10Br2O4
分子量 426.05
InChIKey RTWUBZKPEZFNIJ-UHFFFAOYSA-N
SMILES COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C(=CC(=C3)Br)Br)O

 靶点实验

查看更多实验

实验名称:Inhibition of ROCK1 (unknown origin) assessed as residual activity at 10 uM relative ...
来源:ChEMBL
靶标:Rho-associated protein kinase 1
External Id:CHEMBL2447747
实验名称:Potency index, ratio of fisetin IC50 for CK2 (unknown origin) to compound IC50 for re...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL2447746
实验名称:Inhibition of FGFR1 (unknown origin) assessed as residual activity at 10 uM relative ...
来源:ChEMBL
靶标:Fibroblast growth factor receptor 1
External Id:CHEMBL2447751
实验名称:Inhibition of MET (unknown origin) assessed as residual activity at 10 uM relative to...
来源:ChEMBL
靶标:Hepatocyte growth factor receptor
External Id:CHEMBL2447750
实验名称:Inhibition of Aurora kinase A (unknown origin) assessed as residual activity at 10 uM...
来源:ChEMBL
靶标:Aurora kinase A
External Id:CHEMBL2447749
实验名称:Inhibition of TIE2 (unknown origin) assessed as residual activity at 10 uM relative t...
来源:ChEMBL
靶标:Angiopoietin-1 receptor
External Id:CHEMBL2447748
实验名称:Inhibition of ASK1 (unknown origin) assessed as residual activity at 10 uM relative t...
来源:ChEMBL
靶标:Mitogen-activated protein kinase kinase kinase 5
External Id:CHEMBL2447754
实验名称:Inhibition of JNK3 (unknown origin) assessed as residual activity at 10 uM relative t...
来源:ChEMBL
靶标:Mitogen-activated protein kinase 10
External Id:CHEMBL2447752
实验名称:Inhibition of recombinant human CK2 using RRRDDDSDDD as substrate assessed as residua...
来源:ChEMBL
靶标:Casein kinase II subunit alpha
External Id:CHEMBL2447759
实验名称:Inhibition of recombinant human CK2 using RRRDDDSDDD as substrate after 20 mins by be...
来源:ChEMBL
靶标:Casein kinase II subunit alpha
External Id:CHEMBL2447758
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