Compile Data Set for Download or QSAR
Report error Found 48 Enz. Inhib. hit(s) with all data for entry = 6152
TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112481BDBM112481(US8623885, 22)
Affinity DataIC50: 0.650nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112460BDBM112460(US8623885, 1)
Affinity DataIC50: 1.30nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112475BDBM112475(US8623885, 16)
Affinity DataIC50: 1.40nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112464BDBM112464(US8623885, 5)
Affinity DataIC50: 1.5nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112477BDBM112477(US8623885, 18a)
Affinity DataIC50: 1.60nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112469BDBM112469(US8623885, 10)
Affinity DataIC50: 1.70nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112472BDBM112472(US8623885, 13)
Affinity DataIC50: 1.80nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112462BDBM112462(US8623885, 3)
Affinity DataIC50: 1.80nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112463BDBM112463(US8623885, 4)
Affinity DataIC50: 2nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112460BDBM112460(US8623885, 1)
Affinity DataIC50: 2.10nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112497BDBM112497(US8623885, 18b)
Affinity DataIC50: 2.30nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112467BDBM112467(US8623885, 8)
Affinity DataIC50: 2.40nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112464BDBM112464(US8623885, 5)
Affinity DataIC50: 2.40nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112462BDBM112462(US8623885, 3)
Affinity DataIC50: 2.60nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112471BDBM112471(US8623885, 12)
Affinity DataIC50: 2.70nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112476BDBM112476(US8623885, 17)
Affinity DataIC50: 2.90nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112496BDBM112496(US8623885, 37)
Affinity DataIC50: 3nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112474BDBM112474(US8623885, 15)
Affinity DataIC50: 3.10nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112473BDBM112473(US8623885, 14)
Affinity DataIC50: 3.20nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112461BDBM112461(US8623885, 2)
Affinity DataIC50: 3.20nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112465BDBM112465(US8623885, 6)
Affinity DataIC50: 3.30nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112468BDBM112468(US8623885, 9)
Affinity DataIC50: 3.40nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112473BDBM112473(US8623885, 14)
Affinity DataIC50: 4.40nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112461BDBM112461(US8623885, 2)
Affinity DataIC50: 4.5nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112463BDBM112463(US8623885, 4)
Affinity DataIC50: 4.60nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112483BDBM112483(US8623885, 24)
Affinity DataIC50: 4.70nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112489BDBM112489(US8623885, 30)
Affinity DataIC50: 6.30nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112482BDBM112482(US8623885, 23)
Affinity DataIC50: 8.60nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112469BDBM112469(US8623885, 10)
Affinity DataIC50: 10.5nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112475BDBM112475(US8623885, 16)
Affinity DataIC50: 16.5nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112471BDBM112471(US8623885, 12)
Affinity DataIC50: 18.4nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112477BDBM112477(US8623885, 18a)
Affinity DataIC50: 18.8nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112476BDBM112476(US8623885, 17)
Affinity DataIC50: 19.2nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112474BDBM112474(US8623885, 15)
Affinity DataIC50: 20.3nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112466BDBM112466(US8623885, 7)
Affinity DataIC50: 21.4nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112472BDBM112472(US8623885, 13)
Affinity DataIC50: 31.3nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112478BDBM112478(US8623885, 19)
Affinity DataIC50: 33nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112481BDBM112481(US8623885, 22)
Affinity DataIC50: 36nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112467BDBM112467(US8623885, 8)
Affinity DataIC50: 36.1nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112466BDBM112466(US8623885, 7)
Affinity DataIC50: 52.4nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112468BDBM112468(US8623885, 9)
Affinity DataIC50: 72.8nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112470BDBM112470(US8623885, 11)
Affinity DataIC50: 73.7nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112465BDBM112465(US8623885, 6)
Affinity DataIC50: 120nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112479BDBM112479(US8623885, 20)
Affinity DataIC50: 144nMpH: 7.6Assay Description:The FLT3 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a HTRF kinase assay. The FLT3 enzyme (GST-FLT3 fusion) was purchased f...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112470BDBM112470(US8623885, 11)
Affinity DataIC50: 257nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112497BDBM112497(US8623885, 18b)
Affinity DataIC50: 463nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112479BDBM112479(US8623885, 20)
Affinity DataIC50: 847nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent

TargetCyclin-dependent kinase 4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 112478BDBM112478(US8623885, 19)
Affinity DataIC50: 1.79E+3nMpH: 7.4Assay Description:The CDK4 and CDK1 inhibitory activity of the CDK4/6-FLT3 inhibitors was determined with a filtration kinase assay. The compounds, kinase and substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2014
Entry Details
US Patent