Compile Data Set for Download or QSAR
Report error Found 96 Enz. Inhib. hit(s) with all data for entry = 50019426
TargetTyrosine-protein kinase JAK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50559284BDBM50559284(CHEMBL4753549)
Affinity DataIC50: 3nMAssay Description:Inhibition of JAK2 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619105BDBM50619105(CHEMBL5440964)
Affinity DataIC50: 3nMAssay Description:Inhibition of JAK2 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619108BDBM50619108(CHEMBL5408994)
Affinity DataIC50: 4nMAssay Description:Inhibition of JAK2 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619113BDBM50619113(CHEMBL5419978)
Affinity DataIC50: 5nMAssay Description:Inhibition of JAK2 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619109BDBM50619109(CHEMBL5422938)
Affinity DataIC50: 5nMAssay Description:Inhibition of JAK2 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619110BDBM50619110(CHEMBL5424098)
Affinity DataIC50: 6nMAssay Description:Inhibition of JAK2 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619103BDBM50619103(CHEMBL5403283)
Affinity DataIC50: 7nMAssay Description:Inhibition of JAK2 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619107BDBM50619107(CHEMBL5432626)
Affinity DataIC50: 8nMAssay Description:Inhibition of JAK2 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619118BDBM50619118(CHEMBL5429799)
Affinity DataIC50: 10nMAssay Description:Inhibition of FLT3 in human MOLM-13 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619114BDBM50619114(CHEMBL5398984)
Affinity DataIC50: 10nMAssay Description:Inhibition of FLT3 in human MOLM-13 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619115BDBM50619115(CHEMBL5416946)
Affinity DataIC50: 10nMAssay Description:Inhibition of FLT3 in human MOLM-13 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Mouse)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619109BDBM50619109(CHEMBL5422938)
Affinity DataIC50: 25nMAssay Description:Inhibition of JAK2 V617F mutant in mouse BaF3 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetNon-receptor tyrosine-protein kinase TYK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619105BDBM50619105(CHEMBL5440964)
Affinity DataIC50: 33nMAssay Description:Inhibition of TYK2 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Mouse)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50559284BDBM50559284(CHEMBL4753549)
Affinity DataIC50: 41nMAssay Description:Inhibition of JAK2 V617F mutant in mouse BaF3 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK1(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50559284BDBM50559284(CHEMBL4753549)
Affinity DataIC50: 42nMAssay Description:Inhibition of JAK1 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK1(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619103BDBM50619103(CHEMBL5403283)
Affinity DataIC50: 43nMAssay Description:Inhibition of JAK1 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetNon-receptor tyrosine-protein kinase TYK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619103BDBM50619103(CHEMBL5403283)
Affinity DataIC50: 43nMAssay Description:Inhibition of TYK2 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619109BDBM50619109(CHEMBL5422938)
Affinity DataIC50: 44nMAssay Description:Inhibition of JAK2 V617F mutant in human SET2 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Mouse)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619113BDBM50619113(CHEMBL5419978)
Affinity DataIC50: 53nMAssay Description:Inhibition of JAK2 V617F mutant in mouse BaF3 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK3(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619103BDBM50619103(CHEMBL5403283)
Affinity DataIC50: 54nMAssay Description:Inhibition of JAK3 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50559284BDBM50559284(CHEMBL4753549)
Affinity DataIC50: 62nMAssay Description:Inhibition of FLT3 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetNon-receptor tyrosine-protein kinase TYK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619108BDBM50619108(CHEMBL5408994)
Affinity DataIC50: 62nMAssay Description:Inhibition of TYK2 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Mouse)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619110BDBM50619110(CHEMBL5424098)
Affinity DataIC50: 69nMAssay Description:Inhibition of JAK2 V617F mutant in mouse BaF3 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Mouse)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619108BDBM50619108(CHEMBL5408994)
Affinity DataIC50: 72nMAssay Description:Inhibition of JAK2 V617F mutant in mouse BaF3 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK1(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619105BDBM50619105(CHEMBL5440964)
Affinity DataIC50: 73nMAssay Description:Inhibition of JAK1 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetNon-receptor tyrosine-protein kinase TYK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50559284BDBM50559284(CHEMBL4753549)
Affinity DataIC50: 75nMAssay Description:Inhibition of TYK2 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetNon-receptor tyrosine-protein kinase TYK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619107BDBM50619107(CHEMBL5432626)
Affinity DataIC50: 77nMAssay Description:Inhibition of TYK2 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK1(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619108BDBM50619108(CHEMBL5408994)
Affinity DataIC50: 87nMAssay Description:Inhibition of JAK1 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Mouse)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619103BDBM50619103(CHEMBL5403283)
Affinity DataIC50: 88nMAssay Description:Inhibition of JAK2 V617F mutant in mouse BaF3 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK3(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50559284BDBM50559284(CHEMBL4753549)
Affinity DataIC50: 94nMAssay Description:Inhibition of JAK3 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Mouse)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619105BDBM50619105(CHEMBL5440964)
Affinity DataIC50: 98nMAssay Description:Inhibition of JAK2 V617F mutant in mouse BaF3 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Mouse)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619111BDBM50619111(CHEMBL5408539)
Affinity DataIC50: 101nMAssay Description:Inhibition of JAK2 V617F mutant in mouse BaF3 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK1(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619107BDBM50619107(CHEMBL5432626)
Affinity DataIC50: 106nMAssay Description:Inhibition of JAK1 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619103BDBM50619103(CHEMBL5403283)
Affinity DataIC50: 108nMAssay Description:Inhibition of FLT3 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619111BDBM50619111(CHEMBL5408539)
Affinity DataIC50: 108nMAssay Description:Inhibition of JAK2 V617F mutant in human SET2 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619113BDBM50619113(CHEMBL5419978)
Affinity DataIC50: 109nMAssay Description:Inhibition of JAK2 V617F mutant in human SET2 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Mouse)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619107BDBM50619107(CHEMBL5432626)
Affinity DataIC50: 129nMAssay Description:Inhibition of JAK2 V617F mutant in mouse BaF3 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK1(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619110BDBM50619110(CHEMBL5424098)
Affinity DataIC50: 142nMAssay Description:Inhibition of JAK1 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619105BDBM50619105(CHEMBL5440964)
Affinity DataIC50: 150nMAssay Description:Inhibition of JAK2 V617F mutant in human SET2 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK3(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619108BDBM50619108(CHEMBL5408994)
Affinity DataIC50: 156nMAssay Description:Inhibition of JAK3 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK3(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619105BDBM50619105(CHEMBL5440964)
Affinity DataIC50: 166nMAssay Description:Inhibition of JAK3 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Mouse)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619119BDBM50619119(CHEMBL5404973)
Affinity DataIC50: 170nMAssay Description:Inhibition of JAK2 V617F mutant in mouse BaF3 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Mouse)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619116BDBM50619116(CHEMBL5437784)
Affinity DataIC50: 178nMAssay Description:Inhibition of JAK2 V617F mutant in mouse BaF3 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK1(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619113BDBM50619113(CHEMBL5419978)
Affinity DataIC50: 178nMAssay Description:Inhibition of JAK1 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Mouse)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619112BDBM50619112(CHEMBL5429688)
Affinity DataIC50: 182nMAssay Description:Inhibition of JAK2 V617F mutant in mouse BaF3 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetNon-receptor tyrosine-protein kinase TYK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619110BDBM50619110(CHEMBL5424098)
Affinity DataIC50: 192nMAssay Description:Inhibition of TYK2 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK1(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619109BDBM50619109(CHEMBL5422938)
Affinity DataIC50: 193nMAssay Description:Inhibition of JAK1 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetNon-receptor tyrosine-protein kinase TYK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619113BDBM50619113(CHEMBL5419978)
Affinity DataIC50: 204nMAssay Description:Inhibition of TYK2 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619108BDBM50619108(CHEMBL5408994)
Affinity DataIC50: 205nMAssay Description:Inhibition of JAK2 V617F mutant in human SET2 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Human)
The Affiliated Hospital of Southwest Jiaotong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50619105BDBM50619105(CHEMBL5440964)
Affinity DataIC50: 206nMAssay Description:Inhibition of FLT3 (unknown origin) in presence of Mg/ATP mixture by [gamma p33]-ATP based radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
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