Compile Data Set for Download or QSAR
Found 110 with Last Name = 'aboagye' and Initial = 'eo'
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50326519((E)-N-(4-(3-chloro-4-fluorophenylamino)-3-cyano-7-...)copy SMILEScopy InChI
Affinity DataIC50: 0.0300nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GG2PubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM31090((E)-N-[4-(3-chloro-4-fluoro-anilino)-3-cyano-7-eth...)copy SMILEScopy InChI
Affinity DataIC50: 0.240nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GG2PubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50326514((E)-4-(Methylamino)-but-2-enoic acid [4-(3-chloro-...)copy SMILEScopy InChI
Affinity DataIC50: 0.25nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GG2PubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50326513((E)-4-Methylamino-but-2-enoicacid[4-(3-chloro-4-fl...)copy SMILEScopy InChI
Affinity DataIC50: 0.290nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GG2PubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50326517((E)-4-[(4-Fluorobenzyl)methylamino]-but-2-enoic ac...)copy SMILEScopy InChI
Affinity DataIC50: 0.570nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GG2PubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50326518((E)-4-[(2-Fluoroethyl)methylamino]-but-2-enoic aci...)copy SMILEScopy InChI
Affinity DataIC50: 0.800nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GG2PubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM3303(4-Anilinoquinazoline deriv. 54 | 4-N-(3-bromopheny...)copy SMILEScopy InChI
Affinity DataIC50: 0.810nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GG2PubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50326516((E)-4-{[1-(2-Fluoroethyl)-1H-[1,2,3]triazol-4-ylme...)copy SMILEScopy InChI
Affinity DataIC50: 1.81nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GG2PubMed
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50347388(CHEMBL1234833)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of CDK2/cyclinE assessed as amount of ATP released by luciferase activity based PKLight assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50326515((E)-N-[4-(3-Chloro-4-fluorophenylamino)-3-cyano-7-...)copy SMILEScopy InChI
Affinity DataIC50: 4.05nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GG2PubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50326514((E)-4-(Methylamino)-but-2-enoic acid [4-(3-chloro-...)copy SMILEScopy InChI
Affinity DataIC50: 5.35nMAssay Description:Inhibition of EGFR autophosphorylation in human A431 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GG2PubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM31090((E)-N-[4-(3-chloro-4-fluoro-anilino)-3-cyano-7-eth...)copy SMILEScopy InChI
Affinity DataIC50: 8.02nMAssay Description:Inhibition of EGFR autophosphorylation in human A431 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GG2PubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50326513((E)-4-Methylamino-but-2-enoicacid[4-(3-chloro-4-fl...)copy SMILEScopy InChI
Affinity DataIC50: 8.12nMAssay Description:Inhibition of EGFR autophosphorylation in human A431 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GG2PubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50326517((E)-4-[(4-Fluorobenzyl)methylamino]-but-2-enoic ac...)copy SMILEScopy InChI
Affinity DataIC50: 16.5nMAssay Description:Inhibition of EGFR autophosphorylation in human A431 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GG2PubMed
TargetCyclin-H/Cyclin-dependent kinase 7(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50347389(CHEMBL1801932)copy SMILEScopy InChI
Affinity DataIC50: 21nMAssay Description:Inhibition of CDK7/cyclinH/MAT1 assessed as amount of ATP released by luciferase activity based PKLight assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50326516((E)-4-{[1-(2-Fluoroethyl)-1H-[1,2,3]triazol-4-ylme...)copy SMILEScopy InChI
Affinity DataIC50: 22.0nMAssay Description:Inhibition of EGFR autophosphorylation in human A431 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GG2PubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50326518((E)-4-[(2-Fluoroethyl)methylamino]-but-2-enoic aci...)copy SMILEScopy InChI
Affinity DataIC50: 23.0nMAssay Description:Inhibition of EGFR autophosphorylation in human A431 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GG2PubMed
TargetCyclin-dependent kinase/G2/mitotic-specific cyclin- 1(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50347388(CHEMBL1234833)copy SMILEScopy InChI
Affinity DataIC50: 33nMAssay Description:Inhibition of CDK1/cyclinB1 assessed as amount of ATP released by luciferase activity based PKLight assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50326519((E)-N-(4-(3-chloro-4-fluorophenylamino)-3-cyano-7-...)copy SMILEScopy InChI
Affinity DataIC50: 60.2nMAssay Description:Inhibition of EGFR autophosphorylation in human A431 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GG2PubMed
TargetCyclin-T1/Cyclin-dependent kinase 9(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50347388(CHEMBL1234833)copy SMILEScopy InChI
Affinity DataIC50: 90nMAssay Description:Inhibition of CDK9/cyclinT assessed as amount of ATP released by luciferase activity based PKLight assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM7533((2R)-2-[[6-(benzylamino)-9-isopropyl-purin-2-yl]am...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of CDK2/cyclinE assessed as amount of ATP released by luciferase activity based PKLight assayMore data for this Ligand-Target Pair
TargetCyclin-H/Cyclin-dependent kinase 7(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50347388(CHEMBL1234833)copy SMILEScopy InChI
Affinity DataIC50: 250nMAssay Description:Inhibition of CDK7/cyclinH/MAT1 assessed as amount of ATP released by luciferase activity based PKLight assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetMitogen-activated protein kinase 15(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50347388(CHEMBL1234833)copy SMILEScopy InChI
Affinity DataIC50: 330nMAssay Description:Inhibition of ERK8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetCyclin-H/Cyclin-dependent kinase 7(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM7533((2R)-2-[[6-(benzylamino)-9-isopropyl-purin-2-yl]am...)copy SMILEScopy InChI
Affinity DataIC50: 540nMAssay Description:Inhibition of CDK7/cyclinH/MAT1 assessed as amount of ATP released by luciferase activity based PKLight assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetCyclin-T1/Cyclin-dependent kinase 9(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM7533((2R)-2-[[6-(benzylamino)-9-isopropyl-purin-2-yl]am...)copy SMILEScopy InChI
Affinity DataIC50: 950nMAssay Description:Inhibition of CDK9/cyclinT assessed as amount of ATP released by luciferase activity based PKLight assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50326515((E)-N-[4-(3-Chloro-4-fluorophenylamino)-3-cyano-7-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of EGFR autophosphorylation in human A431 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GG2PubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM3303(4-Anilinoquinazoline deriv. 54 | 4-N-(3-bromopheny...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of EGFR autophosphorylation in human A431 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GG2PubMed
TargetCasein kinase I isoform alpha(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50347388(CHEMBL1234833)copy SMILEScopy InChI
Affinity DataIC50: 1.04E+3nMAssay Description:Inhibition of CK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetInsulin receptor-related protein(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50347388(CHEMBL1234833)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+3nMAssay Description:Inhibition of IRRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetCyclin-dependent kinase/G2/mitotic-specific cyclin- 1(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM7533((2R)-2-[[6-(benzylamino)-9-isopropyl-purin-2-yl]am...)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of CDK1/cyclinB1 assessed as amount of ATP released by luciferase activity based PKLight assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetDual specificity tyrosine-phosphorylation-regulated kinase 1A(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50347388(CHEMBL1234833)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of DYRK1AMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetCalcium/calmodulin-dependent protein kinase kinase 2(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50347388(CHEMBL1234833)copy SMILEScopy InChI
Affinity DataIC50: 2.45E+3nMAssay Description:Inhibition of CAMKKbetaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetMitogen-activated protein kinase 1(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50347388(CHEMBL1234833)copy SMILEScopy InChI
Affinity DataIC50: 3.11E+3nMAssay Description:Inhibition of ERK2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetMitogen-activated protein kinase 3(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50347388(CHEMBL1234833)copy SMILEScopy InChI
Affinity DataIC50: 3.73E+3nMAssay Description:Inhibition of ERK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM7533((2R)-2-[[6-(benzylamino)-9-isopropyl-purin-2-yl]am...)copy SMILEScopy InChI
Affinity DataIC50: 1.35E+4nMAssay Description:Inhibition of CDK4/cyclinD1 assessed as amount of ATP released by luciferase activity based PKLight assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50347388(CHEMBL1234833)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of CDK4/cyclinD1 assessed as amount of ATP released by luciferase activity based PKLight assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetCyclin-dependent kinase 6/G1/S-specific cyclin-D1(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM7533((2R)-2-[[6-(benzylamino)-9-isopropyl-purin-2-yl]am...)copy SMILEScopy InChI
Affinity DataIC50: 2.35E+4nMAssay Description:Inhibition of CDK6/cyclinD1 assessed as amount of ATP released by luciferase activity based PKLight assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetCyclin-dependent kinase 6/G1/S-specific cyclin-D1(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50347388(CHEMBL1234833)copy SMILEScopy InChI
Affinity DataIC50: 3.55E+4nMAssay Description:Inhibition of CDK6/cyclinD1 assessed as amount of ATP released by luciferase activity based PKLight assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858GZPubMed
TargetCaspase-3(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50273926(1-(4-Fluorobenzyl)-5-(pyrrolidine-1-sulfonyl)isati...)copy SMILEScopy InChI
Affinity DataEC50:  200nMAssay Description:Inhibition of human recombinant caspase 3 assessed as accumulation of 7-amino-4-methylcoumarin substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZK5GHKPubMed
TargetCaspase-3(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50273927((S)-1-(4-Fluorobenzyl)-5-(2-(4-fluorophenoxymethyl...)copy SMILEScopy InChI
Affinity DataEC50:  26.1nMAssay Description:Inhibition of human recombinant caspase 3 assessed as accumulation of 7-amino-4-methylcoumarin substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZK5GHKPubMed
TargetCaspase-3(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50273928((S)-1-(4-Fluorobenzyl)-5-(2-(3-fluorophenoxymethyl...)copy SMILEScopy InChI
Affinity DataEC50:  17nMAssay Description:Inhibition of human recombinant caspase 3 assessed as accumulation of 7-amino-4-methylcoumarin substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZK5GHKPubMed
TargetCaspase-3(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50273929((S)-1-(4-Fluorobenzyl)-5-(2-(2,4-difluorophenoxyme...)copy SMILEScopy InChI
Affinity DataEC50:  12.4nMAssay Description:Inhibition of human recombinant caspase 3 assessed as accumulation of 7-amino-4-methylcoumarin substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZK5GHKPubMed
TargetCaspase-3(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50273989((S)-1-(4-Fluorobenzyl)-5-(2-(3,5-difluorophenoxyme...)copy SMILEScopy InChI
Affinity DataEC50:  16.8nMAssay Description:Inhibition of human recombinant caspase 3 assessed as accumulation of 7-amino-4-methylcoumarin substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZK5GHKPubMed
TargetCaspase-3(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50273990((S)-1-(4-Fluorobenzyl)-5-(2-(tetrahydro-2H-pyran-4...)copy SMILEScopy InChI
Affinity DataEC50:  2.30nMAssay Description:Inhibition of human recombinant caspase 3 assessed as accumulation of 7-amino-4-methylcoumarin substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZK5GHKPubMed
TargetCaspase-3(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50273991((S)-1-(4-Fluorobenzyl)-5-(2-(pyrimidin-4-yloxymeth...)copy SMILEScopy InChI
Affinity DataEC50:  5.5nMAssay Description:Inhibition of human recombinant caspase 3 assessed as accumulation of 7-amino-4-methylcoumarin substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZK5GHKPubMed
TargetCaspase-3(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50273992((S)-1-(2-Propynyl)-5-(2-(2,4-difluorophenoxymethyl...)copy SMILEScopy InChI
Affinity DataEC50:  50.1nMAssay Description:Inhibition of human recombinant caspase 3 assessed as accumulation of 7-amino-4-methylcoumarin substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZK5GHKPubMed
TargetCaspase-3(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50273337((S)-1-((1-(2-Fluoroethyl)-1H-[1,2,3]-triazol-4-yl)...)copy SMILEScopy InChI
Affinity DataEC50:  16.7nMAssay Description:Inhibition of human recombinant caspase 3 assessed as accumulation of 7-amino-4-methylcoumarin substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZK5GHKPubMed
TargetCaspase-3(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50273338((S)-1-((1-(2-Fluoroethyl)-1H-[1,2,3]-triazol-4-yl)...)copy SMILEScopy InChI
Affinity DataEC50:  0.5nMAssay Description:Inhibition of human recombinant caspase 3 assessed as accumulation of 7-amino-4-methylcoumarin substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZK5GHKPubMed
TargetCaspase-3(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50273339((S)-1-(4-Fluorobenzyl)-5-(2-((1-(2-fluoroethyl)-1H...)copy SMILEScopy InChI
Affinity DataEC50:  12.6nMAssay Description:Inhibition of human recombinant caspase 3 assessed as accumulation of 7-amino-4-methylcoumarin substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZK5GHKPubMed
TargetCaspase-7(Homo sapiens (Human))
Imperial College London

Curated by ChEMBL
LigandPNGBDBM10323((S)-1-Benzyl-5-{1-[2-(phenoxymethyl)pyrrolidinyl]s...)copy SMILEScopy InChI
Affinity DataEC50:  29.4nMAssay Description:Inhibition of human recombinant caspase 7 assessed as accumulation of 7-amino-4-methylcoumarin substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZK5GHKPubMed
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