BDBM50594716 CHEMBL5191956
SMILES COc1cc(NC(=O)CCCCCCC(=O)NO)ccc1Nc1nccc(n1)-c1cn(C)c2ccccc12
InChI Key InChIKey=WUPDRBBYEINKAK-UHFFFAOYSA-N
Data 9 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 9 hits for monomerid = 50594716
TargetEpidermal growth factor receptor(Human)
Zhuhai Campus of Zunyi Medical University
Curated by ChEMBL
Zhuhai Campus of Zunyi Medical University
Curated by ChEMBL
Affinity DataIC50: 5.70E+3nMAssay Description:Inhibition of wild type EGFR (unknown origin) incubated for 40 mins by Kinase-Glo Plus luminescence kinase assayMore data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Human)
Zhuhai Campus of Zunyi Medical University
Curated by ChEMBL
Zhuhai Campus of Zunyi Medical University
Curated by ChEMBL
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of EGFR T790M mutant (unknown origin) incubated for 40 mins by Kinase-Glo Plus luminescence kinase assayMore data for this Ligand-Target Pair
Affinity DataIC50: 85nMAssay Description:Inhibition of HDAC in human HeLa cell nuclear extract using Boc-Lys (acetyl)-AMC as substrate preincubated for 5 mins followed by substrate addition ...More data for this Ligand-Target Pair
Affinity DataIC50: 85nMAssay Description:Inhibition of HDAC1 in human HeLa cell nuclear extract using Bos-Lys(acetyl)-AMC as substrate preincubated for 5 mins followed by substrate addition ...More data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Human)
Zhuhai Campus of Zunyi Medical University
Curated by ChEMBL
Zhuhai Campus of Zunyi Medical University
Curated by ChEMBL
Affinity DataIC50: 5.90E+3nMAssay Description:Inhibition of EGFR wildtype (unknown origin) incubated for 40 mins in presence of ATPMore data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Human)
Zhuhai Campus of Zunyi Medical University
Curated by ChEMBL
Zhuhai Campus of Zunyi Medical University
Curated by ChEMBL
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of EGFR T790M (unknown origin) incubated for 40 mins in presence of ATPMore data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Human)
Zhuhai Campus of Zunyi Medical University
Curated by ChEMBL
Zhuhai Campus of Zunyi Medical University
Curated by ChEMBL
Affinity DataIC50: 5.70E+3nMAssay Description:Inhibition of wild type EGFR (unknown origin) incubated for 40 mins in presence of ATP by kinase-glo plus luminescence assayMore data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Human)
Zhuhai Campus of Zunyi Medical University
Curated by ChEMBL
Zhuhai Campus of Zunyi Medical University
Curated by ChEMBL
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of EGFR T790M mutant (unknown origin) incubated for 40 mins in presence of ATP by kinase-glo plus luminescence assayMore data for this Ligand-Target Pair
Affinity DataIC50: 85nMAssay Description:Inhibition of HDAC in human HeLa cell nuclear extract using Boc-Lys (acetyl)-AMC as substrate preincubated for 5 mins followed by substrate addition ...More data for this Ligand-Target Pair