Compile Data Set for Download or QSAR
Found 11 from Institute of Molecular Physiology
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Institute of Molecular Physiology

Curated by ChEMBL
LigandPNGBDBM4367((3Z)-2-amino-3-[(3,4,5-trihydroxyphenyl)methyliden...)copy SMILEScopy InChI
Affinity DataIC50: 800nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046C4PubMed
TargetPotassium voltage-gated channel subfamily A member 3(Homo sapiens (Human))
Institute of Molecular Physiology

Curated by ChEMBL
LigandPNGBDBM50265823(CHEMBL516634 | candelalide B)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of voltage-gated Kv1.3 potassium channel (unknown origin) expressed in CHO cells by 86Rb efflux experimentMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2R21172PubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Institute of Molecular Physiology

Curated by ChEMBL
LigandPNGBDBM4363((2E)-2-cyano-3-(3,4-dihydroxyphenyl)prop-2-enethio...)copy SMILEScopy InChI
Affinity DataIC50: 2.40E+3nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046C4PubMed
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Institute of Molecular Physiology

Curated by ChEMBL
LigandPNGBDBM24941((2Z)-2-{[(2,5-dibromophenyl)amino](hydroxy)methyli...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibition of BTKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046C4PubMed
TargetPotassium voltage-gated channel subfamily A member 3(Homo sapiens (Human))
Institute of Molecular Physiology

Curated by ChEMBL
LigandPNGBDBM50265824(CHEMBL460814 | candelalide C)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibition of voltage-gated Kv1.3 potassium channel (unknown origin) expressed in CHO cells by 86Rb efflux experimentMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2R21172PubMed
TargetPotassium voltage-gated channel subfamily A member 3(Homo sapiens (Human))
Institute of Molecular Physiology

Curated by ChEMBL
LigandPNGBDBM50266317(CHEMBL515037 | candelalide A)copy SMILEScopy InChI
Affinity DataIC50: 3.70E+3nMAssay Description:Inhibition of voltage-gated Kv1.3 potassium channel (unknown origin) expressed in CHO cells by 86Rb efflux experimentMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2R21172PubMed
TargetPotassium voltage-gated channel subfamily A member 3(Homo sapiens (Human))
Institute of Molecular Physiology

Curated by ChEMBL
LigandPNGBDBM50265825(CHEMBL516932 | Nalanthalide)copy SMILEScopy InChI
Affinity DataIC50: 3.90E+3nMAssay Description:Antagonist activity at voltage-gated Kv1.3 potassium channel (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2R21172PubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Institute of Molecular Physiology

Curated by ChEMBL
LigandPNGBDBM5718(2,6,9-Trisubstituted purine deriv. 26 | 2-{[6-(ben...)copy SMILEScopy InChI
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibition of CDK2/Cyclin BMore data for this Ligand-Target Pair
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Institute of Molecular Physiology

Curated by ChEMBL
LigandPNGBDBM5718(2,6,9-Trisubstituted purine deriv. 26 | 2-{[6-(ben...)copy SMILEScopy InChI
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibition of CDK2/Cyclin EMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase 3(Homo sapiens (Human))
Institute of Molecular Physiology

Curated by ChEMBL
LigandPNGBDBM5718(2,6,9-Trisubstituted purine deriv. 26 | 2-{[6-(ben...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibition of ERK1/MAPKMore data for this Ligand-Target Pair
TargetInsulin receptor(Homo sapiens (Human))
Institute of Molecular Physiology

Curated by ChEMBL
LigandPNGBDBM4363((2E)-2-cyano-3-(3,4-dihydroxyphenyl)prop-2-enethio...)copy SMILEScopy InChI
Affinity DataIC50: 6.40E+5nMAssay Description:Inhibition of IRKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046C4PubMed