BDBM50613207 CHEMBL5266481

SMILES COc1cc(cc(OC)c1C)-c1nn2C(CCNc2c1C(N)=O)C1CCN(CC1)C(=O)C=C

InChI Key InChIKey=ZFDGMDVYMNWICG-UHFFFAOYSA-N

Data  4 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50613207   

TargetTyrosine-protein kinase BTK(Human)
Beigene (Beijing) Co.

Curated by ChEMBL
LigandPNGBDBM50613207(CHEMBL5266481)
Affinity DataIC50: 1.70nMAssay Description:Inhibition of N-terminal His-tagged recombinant human BTK (393 to 659 residues) expressed in baculovirus infected Sf9 cells using Biotin-AVLESEEELYSS...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMed
TargetEpidermal growth factor receptor(Human)
Beigene (Beijing) Co.

Curated by ChEMBL
LigandPNGBDBM50613207(CHEMBL5266481)
Affinity DataIC50: 3.33E+3nMAssay Description:Inhibition of EGFR (unknown origin) preincubated for 1 hrs followed by substrate addition and measured after 1 hrs in the presence of ATP at Km conce...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMed
TargetTyrosine-protein kinase Tec(Human)
Beigene (Beijing) Co.

Curated by ChEMBL
LigandPNGBDBM50613207(CHEMBL5266481)
Affinity DataIC50: 216nMAssay Description:Inhibition of TEC (unknown origin) preincubated for 1 hrs followed by substrate addition and measured after 1 hrs in the presence of ATP at Km concen...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMed
TargetTyrosine-protein kinase BTK(Human)
Beigene (Beijing) Co.

Curated by ChEMBL
LigandPNGBDBM50613207(CHEMBL5266481)
Affinity DataIC50: 33nMAssay Description:Inhibition of BTK phosphorylation at Tyr 223 residue in human Ramos cell incubated for 3 hrs by HTRF-based analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMed