Compile Data Set for Download or QSAR
Report error Found 18 Enz. Inhib. hit(s) with all data for entry = 50043948
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Pisa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50448811BDBM50448811(CHEMBL3128229)
Affinity DataIC50: 4.26E+3nMAssay Description:Inhibition of recombinant human RET incubated for 5 mins with substrate prior to protein addition by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Pisa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50448821BDBM50448821(CHEMBL3128237)
Affinity DataIC50: 4.80E+3nMAssay Description:Inhibition of recombinant human RET incubated for 5 mins with substrate prior to protein addition by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Pisa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50448815BDBM50448815(CHEMBL3128222)
Affinity DataIC50: 4.83E+3nMAssay Description:Inhibition of recombinant human RET incubated for 5 mins with substrate prior to protein addition by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Pisa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50448823BDBM50448823(CHEMBL3128235)
Affinity DataIC50: 7.04E+3nMAssay Description:Inhibition of recombinant human RET incubated for 5 mins with substrate prior to protein addition by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Pisa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50448817BDBM50448817(CHEMBL3128220)
Affinity DataIC50: 7.90E+3nMAssay Description:Inhibition of recombinant human RET incubated for 5 mins with substrate prior to protein addition by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Pisa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50448822BDBM50448822(CHEMBL3128236)
Affinity DataIC50: 9.07E+3nMAssay Description:Inhibition of recombinant human RET incubated for 5 mins with substrate prior to protein addition by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Pisa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50448820BDBM50448820(CHEMBL3128239)
Affinity DataIC50: 9.26E+3nMAssay Description:Inhibition of recombinant human RET incubated for 5 mins with substrate prior to protein addition by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Pisa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50448810BDBM50448810(CHEMBL3128230)
Affinity DataIC50: 9.64E+3nMAssay Description:Inhibition of recombinant human RET incubated for 5 mins with substrate prior to protein addition by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Pisa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50448818BDBM50448818(CHEMBL3128219)
Affinity DataIC50: 1.03E+4nMAssay Description:Inhibition of recombinant human RET incubated for 5 mins with substrate prior to protein addition by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Pisa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50448816BDBM50448816(CHEMBL3128221)
Affinity DataIC50: 1.29E+4nMAssay Description:Inhibition of recombinant human RET incubated for 5 mins with substrate prior to protein addition by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Pisa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50448819BDBM50448819(CHEMBL3128218)
Affinity DataIC50: 1.53E+4nMAssay Description:Inhibition of recombinant human RET incubated for 5 mins with substrate prior to protein addition by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Pisa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50448809BDBM50448809(CHEMBL3128231)
Affinity DataIC50: 1.71E+4nMAssay Description:Inhibition of recombinant human RET incubated for 5 mins with substrate prior to protein addition by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Pisa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50448812BDBM50448812(CHEMBL3128228)
Affinity DataIC50: 2.24E+4nMAssay Description:Inhibition of recombinant human RET incubated for 5 mins with substrate prior to protein addition by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Pisa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50448824BDBM50448824(CHEMBL3128234)
Affinity DataIC50: 2.26E+4nMAssay Description:Inhibition of recombinant human RET incubated for 5 mins with substrate prior to protein addition by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Pisa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50448808BDBM50448808(CHEMBL3128232)
Affinity DataIC50: 2.41E+4nMAssay Description:Inhibition of recombinant human RET incubated for 5 mins with substrate prior to protein addition by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Pisa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50448807BDBM50448807(CHEMBL3128233)
Affinity DataIC50: 2.81E+4nMAssay Description:Inhibition of recombinant human RET incubated for 5 mins with substrate prior to protein addition by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Pisa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50448814BDBM50448814(CHEMBL3128224)
Affinity DataIC50: 5.72E+4nMAssay Description:Inhibition of recombinant human RET incubated for 5 mins with substrate prior to protein addition by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Pisa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50448813BDBM50448813(CHEMBL3128226)
Affinity DataIC50: 5.86E+4nMAssay Description:Inhibition of recombinant human RET incubated for 5 mins with substrate prior to protein addition by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/26/2014
Entry Details Article
PubMed