Compile Data Set for Download or QSAR
Report error Found 43 Enz. Inhib. hit(s) with all data for entry = 50023697
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50357312BDBM50357312(IBRUTINIB | US9181263, 1 | US9108973, Ref 1 | US92...)
Affinity DataIC50: 0.400nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetTyrosine-protein kinase BTK(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666956BDBM50666956(CHEMBL6171321)
Affinity DataIC50: 4.20nMAssay Description:Inhibition of BTK (unknown origin)More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 194087BDBM194087(US9199997, 9 | US9879013, 19(2) | US20230364079, E...)
Affinity DataIC50: 6nMAssay Description:Inhibition of BMX (unknown origin) incubated for 1 hrs by Z'-LYTE kinase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetTyrosine-protein kinase BTK(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 194087BDBM194087(US9199997, 9 | US9879013, 19(2) | US20230364079, E...)
Affinity DataIC50: 7nMAssay Description:Inhibition of BTK (unknown origin) incubated for 1 hrs by Z'-LYTE kinase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666955BDBM50666955(CHEMBL6176872)
Affinity DataIC50: 7nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 102620BDBM102620(N-[5-[9-[4-(methanesulfonamido)phenyl]-2-oxobenzo[...)
Affinity DataIC50: 8nMAssay Description:Inhibition of BMX (unknown origin) by Invitrogen selectscreen assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetTyrosine-protein kinase BTK(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 102620BDBM102620(N-[5-[9-[4-(methanesulfonamido)phenyl]-2-oxobenzo[...)
Affinity DataIC50: 10nMAssay Description:Inhibition of BTK (unknown origin) by Invitrogen selectscreen assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666953BDBM50666953(CHEMBL6177465)
Affinity DataIC50: 12nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666954BDBM50666954(CHEMBL6176258)
Affinity DataIC50: 21nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetTyrosine-protein kinase Tec(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666953BDBM50666953(CHEMBL6177465)
Affinity DataIC50: 26nMAssay Description:Inhibition of TEC (unknown origin) in presence of ATP at Km concentrationMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666946BDBM50666946(CHEMBL6176612)
Affinity DataIC50: 29nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666948BDBM50666948(CHEMBL6176275)
Affinity DataIC50: 32nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666949BDBM50666949(CHEMBL6165519)
Affinity DataIC50: 46nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666950BDBM50666950(CHEMBL6175361)
Affinity DataIC50: 50nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetEpidermal growth factor receptor(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50357312BDBM50357312(IBRUTINIB | US9181263, 1 | US9108973, Ref 1 | US92...)
Affinity DataIC50: 51nMAssay Description:Inhibition of EGFR T790M mutant (unknown origin) using poly (Glu:Tyr)(4:1) as substrate incubated for 1 hrs in presence of ATP by ADP-Glo reagent bas...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666951BDBM50666951(CHEMBL6172550)
Affinity DataIC50: 86nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetEpidermal growth factor receptor(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666953BDBM50666953(CHEMBL6177465)
Affinity DataIC50: 177nMAssay Description:Inhibition of EGFR T790M (unknown origin) in presence of ATP at Km concentrationMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetTyrosine-protein kinase BTK(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666953BDBM50666953(CHEMBL6177465)
Affinity DataIC50: 187nMAssay Description:Inhibition of BTK (unknown origin) in presence of ATP at Km concentrationMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666938BDBM50666938(CHEMBL6169536)
Affinity DataIC50: 328nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666953BDBM50666953(CHEMBL6177465)
Affinity DataIC50: 392nMAssay Description:Inhibition of HER2 (unknown origin) in presence of ATP at Km concentrationMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetTyrosine-protein kinase JAK3(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666953BDBM50666953(CHEMBL6177465)
Affinity DataIC50: 437nMAssay Description:Inhibition of JAK3 (unknown origin) in presence of ATP at Km concentrationMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetEpidermal growth factor receptor(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666953BDBM50666953(CHEMBL6177465)
Affinity DataIC50: 468nMAssay Description:Inhibition of EGFR (unknown origin) in presence of ATP at Km concentrationMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666931BDBM50666931(CHEMBL6175423)
Affinity DataIC50: 495nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666936BDBM50666936(CHEMBL6177081)
Affinity DataIC50: 614nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetTyrosine-protein kinase Blk(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666953BDBM50666953(CHEMBL6177465)
Affinity DataIC50: 638nMAssay Description:Inhibition of BLK (unknown origin) in presence of ATP at Km concentrationMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666947BDBM50666947(CHEMBL6172481)
Affinity DataIC50: 917nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666935BDBM50666935(CHEMBL6177395)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666937BDBM50666937(CHEMBL6173674)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetReceptor tyrosine-protein kinase erbB-4(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666953BDBM50666953(CHEMBL6177465)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of HER4 (unknown origin) in presence of ATP at Km concentrationMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666932BDBM50666932(CHEMBL6174751)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666933BDBM50666933(CHEMBL6171015)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666934BDBM50666934(CHEMBL6174302)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666943BDBM50666943(CHEMBL6174411)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666944BDBM50666944(CHEMBL6175209)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666945BDBM50666945(CHEMBL6176962)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666939BDBM50666939(CHEMBL6174623)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666940BDBM50666940(CHEMBL6177611)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666941BDBM50666941(CHEMBL6176449)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666942BDBM50666942(CHEMBL6169940)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666952BDBM50666952(CHEMBL6172870)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666929BDBM50666929(CHEMBL6166170)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666930BDBM50666930(CHEMBL6174942)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant human BMX in the presence of ATP at Km concentration by caliper mobility shift assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetTyrosine-protein kinase ITK/TSK(Human)
Zhengzhou University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666953BDBM50666953(CHEMBL6177465)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of ITK (unknown origin) in presence of ATP at Km concentrationMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed