Compile Data Set for Download or QSAR
Found 57 with Last Name = 'bender' and Initial = 'at'
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck KGaA

Curated by ChEMBL
LigandPNGBDBM291573(N-(3-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)a...)copy SMILEScopy InChI
Affinity DataKi:  530nMAssay Description:Inhibition of human ERG expressed in HEK293 cells at -80 mV holding potential by HPLC analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6TXTPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck KGaA

Curated by ChEMBL
LigandPNGBDBM291413(1-(6-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)a...)copy SMILEScopy InChI
Affinity DataKi:  780nMAssay Description:Inhibition of human ERG expressed in HEK293 cells at -80 mV holding potential by HPLC analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6TXTPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck KGaA

Curated by ChEMBL
LigandPNGBDBM291455(N-(4-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)a...)copy SMILEScopy InChI
Affinity DataKi:  1.30E+3nMAssay Description:Inhibition of human ERG expressed in HEK293 cells at -80 mV holding potential by HPLC analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6TXTPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck KGaA

Curated by ChEMBL
LigandPNGBDBM291452(N-((1R,3S)-3-((6-amino-5-(4-phenoxyphenyl)pyrimidi...)copy SMILEScopy InChI
Affinity DataKi:  1.80E+3nMAssay Description:Inhibition of human ERG expressed in HEK293 cells at -80 mV holding potential by HPLC analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6TXTPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck KGaA

Curated by ChEMBL
LigandPNGBDBM291522(1-(4-(((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)...)copy SMILEScopy InChI
Affinity DataKi:  3.10E+3nMAssay Description:Inhibition of human ERG expressed in HEK293 cells at -80 mV holding potential by HPLC analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6TXTPubMed
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck KGaA

Curated by ChEMBL
LigandPNGBDBM50519156(CHEMBL4466205)copy SMILEScopy InChI
Affinity DataIC50: 0.200nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291635(1-(4-(((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 0.200nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291634(1-(4-(((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 0.600nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291389(5-(4-phenoxyphenyl)-N4-((1-(vinylsulfonyl)piperidi...)copy SMILEScopy InChI
Affinity DataIC50: 0.800nMAssay 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
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Merck KGaA

Curated by ChEMBL
LigandPNGBDBM291512(N-(3-(4-amino-6-((4-phenoxyphenyl)amino)pyrimidin-...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of N-terminal GST-tagged human EGFR (696 to end aminoacids) expressed in baculovirus infected Sf21 cellsMore 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291413(1-(6-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)a...)copy SMILEScopy InChI
Affinity DataIC50: 2.10nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291513(N-(3-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)o...)copy SMILEScopy InChI
Affinity DataIC50: 2.90nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291573(N-(3-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)a...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay 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
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Merck KGaA

Curated by ChEMBL
LigandPNGBDBM291573(N-(3-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)a...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of N-terminal GST-tagged human EGFR (696 to end aminoacids) expressed in baculovirus infected Sf21 cellsMore 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291515(N-(3-((2-amino-3-(4-phenoxyphenyl)pyridin-4-yl)oxy...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291425((S)-1-(3-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-...)copy SMILEScopy InChI
Affinity DataIC50: 5.5nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291625(1-(4-(((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 5.90nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291549((S)-1-(3-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-...)copy SMILEScopy InChI
Affinity DataIC50: 6.5nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291512(N-(3-(4-amino-6-((4-phenoxyphenyl)amino)pyrimidin-...)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291522(1-(4-(((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 8.90nMAssay 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
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck KGaA

Curated by ChEMBL
LigandPNGBDBM291610(1-(4-(((6-amino-5-(4-(3-fluorophenoxy)phenyl)pyrim...)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291513(N-(3-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)o...)copy SMILEScopy InChI
Affinity DataIC50: 9.90nMAssay Description:Inhibition of BTK in human PBMC cells assessed as reduction in anti-IgM-stimulated CD69 expression on B cells preincubated for 60 mins followed by go...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 KGaA

Curated by ChEMBL
LigandPNGBDBM291455(N-(4-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)a...)copy SMILEScopy InChI
Affinity DataIC50: 9.90nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291452(N-((1R,3S)-3-((6-amino-5-(4-phenoxyphenyl)pyrimidi...)copy SMILEScopy InChI
Affinity DataIC50: 14nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291684(1-(4-(((6-amino-5-(4-(p-tolyloxy)phenyl)pyrimidin-...)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291573(N-(3-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)a...)copy SMILEScopy InChI
Affinity DataIC50: 19nMAssay Description:Inhibition of BTK in human PBMC cells assessed as reduction in anti-IgM-stimulated CD69 expression on B cells preincubated for 60 mins followed by go...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 KGaA

Curated by ChEMBL
LigandPNGBDBM291460(N-(cis-3-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-...)copy SMILEScopy InChI
Affinity DataIC50: 21nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291527(N-(3-((5-(4-phenoxyphenyl)pyrimidin-4-yl)oxy)pheny...)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291625(1-(4-(((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 26nMAssay Description:Inhibition of BTK in human PBMC cells assessed as reduction in anti-IgM-stimulated CD69 expression on B cells preincubated for 60 mins followed by go...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 KGaA

Curated by ChEMBL
LigandPNGBDBM291539(N-((1s,4s)-4-((6-amino-5-(4-phenoxyphenyl)pyrimidi...)copy SMILEScopy InChI
Affinity DataIC50: 33nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291544(N-(3-((3-(4-phenoxyphenyl)pyridin-4-yl)oxy)phenyl)...)copy SMILEScopy InChI
Affinity DataIC50: 44nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291389(5-(4-phenoxyphenyl)-N4-((1-(vinylsulfonyl)piperidi...)copy SMILEScopy InChI
Affinity DataIC50: 45nMAssay Description:Inhibition of BTK in human PBMC cells assessed as reduction in anti-IgM-stimulated CD69 expression on B cells preincubated for 60 mins followed by go...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 KGaA

Curated by ChEMBL
LigandPNGBDBM291522(1-(4-(((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 61nMAssay Description:Inhibition of BTK in human PBMC cells assessed as reduction in anti-IgM-stimulated CD69 expression on B cells preincubated for 60 mins followed by go...More data for this Ligand-Target Pair
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck KGaA

Curated by ChEMBL
LigandPNGBDBM291413(1-(6-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)a...)copy SMILEScopy InChI
Affinity DataIC50: 66nMAssay Description:Inhibition of BTK in human PBMC cells assessed as reduction in anti-IgM-stimulated CD69 expression on B cells preincubated for 60 mins followed by go...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 KGaA

Curated by ChEMBL
LigandPNGBDBM291455(N-(4-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)a...)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Inhibition of BTK in human PBMC cells assessed as reduction in anti-IgM-stimulated CD69 expression on B cells preincubated for 60 mins followed by go...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6TXTPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Merck KGaA

Curated by ChEMBL
LigandPNGBDBM291513(N-(3-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)o...)copy SMILEScopy InChI
Affinity DataIC50: 78nMAssay Description:Inhibition of N-terminal GST-tagged human EGFR (696 to end aminoacids) expressed in baculovirus infected Sf21 cellsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6TXTPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Merck KGaA

Curated by ChEMBL
LigandPNGBDBM291515(N-(3-((2-amino-3-(4-phenoxyphenyl)pyridin-4-yl)oxy...)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Inhibition of N-terminal GST-tagged human EGFR (696 to end aminoacids) expressed in baculovirus infected Sf21 cellsMore 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291549((S)-1-(3-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-...)copy SMILEScopy InChI
Affinity DataIC50: 143nMAssay Description:Inhibition of BTK in human PBMC cells assessed as reduction in anti-IgM-stimulated CD69 expression on B cells preincubated for 60 mins followed by go...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 KGaA

Curated by ChEMBL
LigandPNGBDBM291668(1-(4-(((6-amino-5-(4-(4-(fluorophenoxy)phenyl)pyri...)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291634(1-(4-(((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 160nMAssay Description:Inhibition of BTK in human PBMC cells assessed as reduction in anti-IgM-stimulated CD69 expression on B cells preincubated for 60 mins followed by go...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 KGaA

Curated by ChEMBL
LigandPNGBDBM291675(1-(4-(((6-amino-5-(2,5-difluoro-4-phenoxyphenyl)py...)copy SMILEScopy InChI
Affinity DataIC50: 160nMAssay 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
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Merck KGaA

Curated by ChEMBL
LigandPNGBDBM50092228(4-Amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrim...)copy SMILEScopy InChI
Affinity DataIC50: 177nMAssay Description:Inhibition of N-terminal GST-tagged human EGFR (696 to end aminoacids) expressed in baculovirus infected Sf21 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6TXTPubMed
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck KGaA

Curated by ChEMBL
LigandPNGBDBM291425((S)-1-(3-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-...)copy SMILEScopy InChI
Affinity DataIC50: 217nMAssay Description:Inhibition of BTK in human PBMC cells assessed as reduction in anti-IgM-stimulated CD69 expression on B cells preincubated for 60 mins followed by go...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 KGaA

Curated by ChEMBL
LigandPNGBDBM291631((4-(((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)am...)copy SMILEScopy InChI
Affinity DataIC50: 290nMAssay Description:Inhibition of BTK in human PBMC cells assessed as reduction in anti-IgM-stimulated CD69 expression on B cells preincubated for 60 mins followed by go...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 KGaA

Curated by ChEMBL
LigandPNGBDBM291631((4-(((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)am...)copy SMILEScopy InChI
Affinity DataIC50: 290nMAssay 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 KGaA

Curated by ChEMBL
LigandPNGBDBM50092228(4-Amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrim...)copy SMILEScopy InChI
Affinity DataIC50: 310nMAssay 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
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6TXTPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Merck KGaA

Curated by ChEMBL
LigandPNGBDBM291549((S)-1-(3-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-...)copy SMILEScopy InChI
Affinity DataIC50: 550nMAssay Description:Inhibition of N-terminal GST-tagged human EGFR (696 to end aminoacids) expressed in baculovirus infected Sf21 cellsMore 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 KGaA

Curated by ChEMBL
LigandPNGBDBM291539(N-((1s,4s)-4-((6-amino-5-(4-phenoxyphenyl)pyrimidi...)copy SMILEScopy InChI
Affinity DataIC50: 660nMAssay Description:Inhibition of BTK in human PBMC cells assessed as reduction in anti-IgM-stimulated CD69 expression on B cells preincubated for 60 mins followed by go...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 KGaA

Curated by ChEMBL
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 KGaA

Curated by ChEMBL
LigandPNGBDBM291434(4-(4-(((1-acryloylpiperidin-4-yl)methyl)amino)-6-a...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+3nMAssay 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
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