Compile Data Set for Download or QSAR
Report error Found 47 Enz. Inhib. hit(s) with all data for entry = 50010916
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543391BDBM50543391(CHEMBL4638277)
Affinity DataIC50: 1.90nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543390BDBM50543390(CHEMBL4643319)
Affinity DataIC50: 2nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543377BDBM50543377(CHEMBL4644207)
Affinity DataIC50: 2.30nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50244440BDBM50244440(CHEMBL4065122)
Affinity DataIC50: 2.30nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543383BDBM50543383(CHEMBL4634904)
Affinity DataIC50: 2.40nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543382BDBM50543382(CHEMBL4648439)
Affinity DataIC50: 3.20nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543378BDBM50543378(CHEMBL4644448)
Affinity DataIC50: 3.80nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543381BDBM50543381(CHEMBL4641507)
Affinity DataIC50: 4.80nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543387BDBM50543387(CHEMBL4646964)
Affinity DataIC50: 5.10nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543366BDBM50543366(CHEMBL4644856)
Affinity DataIC50: 7.10nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543385BDBM50543385(CHEMBL4638307)
Affinity DataIC50: 7.20nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543380BDBM50543380(CHEMBL4649410)
Affinity DataIC50: 7.70nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50244440BDBM50244440(CHEMBL4065122)
Affinity DataIC50: 8nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in anti-IgM-stimulated CD69 expression preincubated for 1 hr followed by goat F(ab')2 an...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543371BDBM50543371(CHEMBL4638562)
Affinity DataIC50: 12nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543368BDBM50543368(CHEMBL4648782)
Affinity DataIC50: 14nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543367BDBM50543367(CHEMBL4646782)
Affinity DataIC50: 15nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543372BDBM50543372(CHEMBL4647342)
Affinity DataIC50: 22nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543386BDBM50543386(CHEMBL4647569)
Affinity DataIC50: 26nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543384BDBM50543384(CHEMBL4633058)
Affinity DataIC50: 32nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543390BDBM50543390(CHEMBL4643319)
Affinity DataIC50: 37nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in anti-IgM-stimulated CD69 expression preincubated for 1 hr followed by goat F(ab')2 an...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543369BDBM50543369(CHEMBL4649614)
Affinity DataIC50: 44nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543376BDBM50543376(CHEMBL4636316)
Affinity DataIC50: 60nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543374BDBM50543374(CHEMBL4638921)
Affinity DataIC50: 74nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543373BDBM50543373(CHEMBL4640083)
Affinity DataIC50: 74nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543383BDBM50543383(CHEMBL4634904)
Affinity DataIC50: 78nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in anti-IgM-stimulated CD69 expression preincubated for 1 hr followed by goat F(ab')2 an...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543381BDBM50543381(CHEMBL4641507)
Affinity DataIC50: 78nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in anti-IgM-stimulated CD69 expression preincubated for 1 hr followed by goat F(ab')2 an...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543379BDBM50543379(CHEMBL4638609)
Affinity DataIC50: 98nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543385BDBM50543385(CHEMBL4638307)
Affinity DataIC50: 110nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in anti-IgM-stimulated CD69 expression preincubated for 1 hr followed by goat F(ab')2 an...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543391BDBM50543391(CHEMBL4638277)
Affinity DataIC50: 125nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in anti-IgM-stimulated CD69 expression preincubated for 1 hr followed by goat F(ab')2 an...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543366BDBM50543366(CHEMBL4644856)
Affinity DataIC50: 140nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in anti-IgM-stimulated CD69 expression preincubated for 1 hr followed by goat F(ab')2 an...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543382BDBM50543382(CHEMBL4648439)
Affinity DataIC50: 180nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in anti-IgM-stimulated CD69 expression preincubated for 1 hr followed by goat F(ab')2 an...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543370BDBM50543370(CHEMBL4639728)
Affinity DataIC50: 200nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543387BDBM50543387(CHEMBL4646964)
Affinity DataIC50: 214nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in anti-IgM-stimulated CD69 expression preincubated for 1 hr followed by goat F(ab')2 an...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543389BDBM50543389(CHEMBL4643339)
Affinity DataIC50: 280nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543375BDBM50543375(CHEMBL4646580)
Affinity DataIC50: 320nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543384BDBM50543384(CHEMBL4633058)
Affinity DataIC50: 326nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in anti-IgM-stimulated CD69 expression preincubated for 1 hr followed by goat F(ab')2 an...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543365BDBM50543365(CHEMBL4638802)
Affinity DataIC50: 360nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543388BDBM50543388(CHEMBL4643297)
Affinity DataIC50: 410nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in autophosphorylation at Y223 residue incubated for 1 hr by mesoscale assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543380BDBM50543380(CHEMBL4649410)
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in anti-IgM-stimulated CD69 expression preincubated for 1 hr followed by goat F(ab')2 an...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50543383BDBM50543383(CHEMBL4634904)
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of human ERG by automated patch clamp assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50543390BDBM50543390(CHEMBL4643319)
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of human ERG by automated patch clamp assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetTyrosine-protein kinase BTK(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543379BDBM50543379(CHEMBL4638609)
Affinity DataIC50: 4.30E+3nMAssay Description:Inhibition of BTK in human whole blood assessed as reduction in anti-IgM-stimulated CD69 expression preincubated for 1 hr followed by goat F(ab')2 an...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetCytochrome P450 4B1(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50244440BDBM50244440(CHEMBL4065122)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human liver microsome CYP450More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
TargetCytochrome P450 4B1(Human)
Genentech

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50543383BDBM50543383(CHEMBL4634904)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human liver microsome CYP450More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50543391BDBM50543391(CHEMBL4638277)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human ERG by automated patch clamp assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50543382BDBM50543382(CHEMBL4648439)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human ERG by automated patch clamp assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50244440BDBM50244440(CHEMBL4065122)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human ERG by automated patch clamp assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/13/2021
Entry Details Article
PubMed