Compile Data Set for Download or QSAR
Report error Found 11 Enz. Inhib. hit(s) with all data for entry = 50008423
TargetVascular endothelial growth factor receptor 2(Human)
Tsinghua University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 16673BDBM16673(BAY439006 | CHEMBL1336 | BAY 43-9006 | 4-[4-({[4-c...)
Affinity DataIC50: 19nMAssay Description:Inhibition of VEGFR2 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/23/2021
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetVascular endothelial growth factor receptor 2(Human)
Tsinghua University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50519223BDBM50519223(CHEMBL4453974)
Affinity DataIC50: 34nMAssay Description:Inhibition of VEGFR2 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/23/2021
Entry Details Article
PubMed
TargetVascular endothelial growth factor receptor 2(Human)
Tsinghua University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50519230BDBM50519230(CHEMBL4520209)
Affinity DataIC50: 34nMAssay Description:Inhibition of VEGFR2 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/23/2021
Entry Details Article
PubMed
TargetVascular endothelial growth factor receptor 2(Human)
Tsinghua University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50519229BDBM50519229(CHEMBL4532350)
Affinity DataIC50: 5.41E+3nMAssay Description:Inhibition of VEGFR2 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/23/2021
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Tsinghua University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50519228BDBM50519228(CHEMBL4439821)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of AKT phosphorylation in human K562 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/23/2021
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Tsinghua University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50519226BDBM50519226(CHEMBL4463428)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of AKT phosphorylation in human K562 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/23/2021
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Tsinghua University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50519227BDBM50519227(CHEMBL4551206)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of AKT phosphorylation in human K562 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/23/2021
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Tsinghua University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50519224BDBM50519224(CHEMBL4464965)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of AKT phosphorylation in human K562 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/23/2021
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Tsinghua University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50519225BDBM50519225(CHEMBL4551568)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of AKT phosphorylation in human K562 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/23/2021
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Tsinghua University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50519231BDBM50519231(CHEMBL4516895)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of AKT phosphorylation in human K562 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/23/2021
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Tsinghua University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50519232BDBM50519232(CHEMBL4570215)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of AKT phosphorylation in human K562 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/23/2021
Entry Details Article
PubMed