null

SMILES Nc1ncnc(NCC2CCN(CC2)C(=O)C=C)c1-c1ccc(Oc2ccncc2)cc1

InChI Key InChIKey=YMJCJOSTNRHERU-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 291683   

TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck Patent GmbH

US Patent
LigandPNGBDBM291683(1-(4-(((6-amino-5-(4-(pyridin-4-yloxy)phenyl)pyrim...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMpH: 7.5 T: 2°CAssay Description:The following describes a microfluidic, off-chip mobility shift kinase assay used to measure inherent potency of compounds against BTK enzyme. Compou...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q28K7C4ZUS Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck Patent GmbH

US Patent
LigandPNGBDBM291683(1-(4-(((6-amino-5-(4-(pyridin-4-yloxy)phenyl)pyrim...)copy SMILEScopy InChI
Affinity DataIC50: 730nMAssay Description:Covalent inhibition of N-terminal GST-fused human BTK (2-659(end) amino acids) expressed in baculovirus expression system using FITC-AHA-EEPLYWSFPAKK...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6TXTPubMed
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck Patent GmbH

US Patent
LigandPNGBDBM291683(1-(4-(((6-amino-5-(4-(pyridin-4-yloxy)phenyl)pyrim...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:2.5× stocks of full-length human BTK (08-080) from CarnaBio USA, Inc., Natick, Mass., 1.6×ATP and appropriate kinKDR peptide substrate (FITC-AHA-EEPL...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0B95US Patent