Compile Data Set for Download or QSAR
Found 1037 from Ferring Research Institute
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068972((S)-3-(2-{3-[(Naphthalene-2-carbonyl)-amino]-2-oxo...)copy SMILEScopy InChI
Affinity DataKi:  0.370nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068954((S)-5-Butylamino-3-(2-{3-[(naphthalene-2-carbonyl)...)copy SMILEScopy InChI
Affinity DataKi:  0.760nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068949((S)-5-Hexylamino-3-(2-{3-[(naphthalene-2-carbonyl)...)copy SMILEScopy InChI
Affinity DataKi:  0.850nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068950((S)-3-(2-{3-[(Naphthalene-2-carbonyl)-amino]-2-oxo...)copy SMILEScopy InChI
Affinity DataKi:  1.20nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068945((S)-5-(Hexyl-methyl-amino)-3-(2-{3-[(naphthalene-2...)copy SMILEScopy InChI
Affinity DataKi:  1.80nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068953((S)-5-(Butyl-ethyl-amino)-3-(2-{3-[(naphthalene-2-...)copy SMILEScopy InChI
Affinity DataKi:  2.30nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068951((S)-5-Dihexylamino-3-(2-{3-[(naphthalene-2-carbony...)copy SMILEScopy InChI
Affinity DataKi:  2.40nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetOxytocin receptor(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50403716(CHEMBL2112378)copy SMILEScopy InChI
Affinity DataKi:  2.80nMAssay Description:In vivo antagonistic activity against cloned human oxytocin receptor overexpressed in a stable HEK293 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3QVVPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068957((S)-5-Benzylamino-3-(2-{3-[(naphthalene-2-carbonyl...)copy SMILEScopy InChI
Affinity DataKi:  3.10nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068962((S)-5-(Butyl-methyl-amino)-3-(2-{3-[(naphthalene-2...)copy SMILEScopy InChI
Affinity DataKi:  3.10nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068967(3-(2-{3-[(Naphthalene-2-carbonyl)-amino]-2-oxo-2H-...)copy SMILEScopy InChI
Affinity DataKi:  4nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068966((S)-5-(Methyl-phenethyl-amino)-3-(2-{3-[(naphthale...)copy SMILEScopy InChI
Affinity DataKi:  4.80nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068965(3-(2-{3-[(Naphthalene-2-carbonyl)-amino]-2-oxo-2H-...)copy SMILEScopy InChI
Affinity DataKi:  7.30nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068952(1-[4-Carboxy-3-(2-{3-[(naphthalene-2-carbonyl)-ami...)copy SMILEScopy InChI
Affinity DataKi:  8nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068955(3-(2-{3-[(Naphthalene-2-carbonyl)-amino]-2-oxo-2H-...)copy SMILEScopy InChI
Affinity DataKi:  11nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068971(5-(4-Carbamoyl-piperidin-1-yl)-3-(2-{3-[(naphthale...)copy SMILEScopy InChI
Affinity DataKi:  12nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068970((S)-5-Dimethylamino-3-(2-{3-[(naphthalene-2-carbon...)copy SMILEScopy InChI
Affinity DataKi:  23nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068969((S)-5-((R)-1-Carbamoyl-2-phenyl-ethylamino)-3-(2-{...)copy SMILEScopy InChI
Affinity DataKi:  25nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetOxytocin receptor(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50081738(2-[(3S,6S,9S,12S,15R)-3-(3-Amino-propyl)-9-((R)-se...)copy SMILEScopy InChI
Affinity DataKi:  26nMAssay Description:In vivo antagonistic activity against cloned human oxytocin receptor overexpressed in a stable HEK293 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3QVVPubMed
TargetOxytocin receptor(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50081738(2-[(3S,6S,9S,12S,15R)-3-(3-Amino-propyl)-9-((R)-se...)copy SMILEScopy InChI
Affinity DataKi:  26nMAssay Description:In vivo antagonistic activity against cloned human oxytocin receptor over-expressed in a stable HEK293 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3QVVPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068973(5-Hexanoylamino-3-(2-{3-[(naphthalene-2-carbonyl)-...)copy SMILEScopy InChI
Affinity DataKi:  34nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068947((S)-5-[(3-Carbamoyl-propyl)-methyl-amino]-3-(2-{3-...)copy SMILEScopy InChI
Affinity DataKi:  37nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068944(5-Morpholin-4-yl-3-(2-{3-[(naphthalene-2-carbonyl)...)copy SMILEScopy InChI
Affinity DataKi:  45nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068968(5-Benzoylamino-3-(2-{3-[(naphthalene-2-carbonyl)-a...)copy SMILEScopy InChI
Affinity DataKi:  58nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068946((S)-5-(Benzyl-methyl-amino)-3-(2-{3-[(naphthalene-...)copy SMILEScopy InChI
Affinity DataKi:  58nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068958(5-(4-Methyl-piperazin-1-yl)-3-(2-{3-[(naphthalene-...)copy SMILEScopy InChI
Affinity DataKi:  63nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068960((S)-5-((S)-1-Carbamoyl-2-phenyl-ethylamino)-3-(2-{...)copy SMILEScopy InChI
Affinity DataKi:  78nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068948(5-Butyrylamino-3-(2-{3-[(naphthalene-2-carbonyl)-a...)copy SMILEScopy InChI
Affinity DataKi:  81nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068963(5-Acetylamino-3-(2-{3-[(naphthalene-2-carbonyl)-am...)copy SMILEScopy InChI
Affinity DataKi:  117nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068959((S)-5-[((S)-1-Carbamoyl-2-phenyl-ethyl)-methyl-ami...)copy SMILEScopy InChI
Affinity DataKi:  255nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068961(3-(2-{3-[(Naphthalene-2-carbonyl)-amino]-2-oxo-2H-...)copy SMILEScopy InChI
Affinity DataKi:  395nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068964(3-(2-{3-[(Naphthalene-2-carbonyl)-amino]-2-oxo-2H-...)copy SMILEScopy InChI
Affinity DataKi:  410nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetOxytocin receptor(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50403717(CHEMBL2112376)copy SMILEScopy InChI
Affinity DataKi:  1.00E+3nMAssay Description:In vivo antagonistic activity against cloned human oxytocin receptor overexpressed in a stable HEK293 cell lineMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3QVVPubMed
TargetCaspase-1(Homo sapiens (Human))
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50068956(3-(2-{3-[(Naphthalene-2-carbonyl)-amino]-2-oxo-2H-...)copy SMILEScopy InChI
Affinity DataKi:  1.65E+3nMAssay Description:Inhibition of human recombinant IL-1 beta converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ZP458CPubMed
TargetGastrin/cholecystokinin type B receptor(RAT)
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50056102((R)-1-(1-(3,3-dimethyl-2-oxobutyl)-2-oxo-5-(pyridi...)copy SMILEScopy InChI
Affinity DataIC50: 0.100nMAssay Description:Inhibitory concentration against radioligand [125I]-CCK-8 binding to gastrin/Cholecystokinin type B receptor from rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BBQPubMed
TargetGastrin/cholecystokinin type B receptor(RAT)
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50056101(1-[(R)-2-Oxo-1-(2-oxo-2-o-tolyl-ethyl)-5-phenyl-2,...)copy SMILEScopy InChI
Affinity DataIC50: 0.110nMAssay Description:Inhibitory concentration against radioligand [125I]-CCK-8 binding to gastrin/Cholecystokinin type B receptor from rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BBQPubMed
TargetGastrin/cholecystokinin type B receptor(RAT)
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50056093(1-[(R)-1-(3,3-Dimethyl-2-oxo-butyl)-2-oxo-5-phenyl...)copy SMILEScopy InChI
Affinity DataIC50: 0.110nMAssay Description:Inhibitory concentration against radioligand [125I]-CCK-8 binding to gastrin/Cholecystokinin type B receptor from rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BBQPubMed
TargetGastrin/cholecystokinin type B receptor(RAT)
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50056099(1-[(R)-1-(3,3-Dimethyl-2-oxo-butyl)-2-oxo-5-pyridi...)copy SMILEScopy InChI
Affinity DataIC50: 0.110nMAssay Description:Inhibitory concentration against radioligand [125I]-CCK-8 binding to gastrin/Cholecystokinin type B receptor from rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BBQPubMed
TargetGastrin/cholecystokinin type B receptor(RAT)
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50056103(1-(3-Diethylamino-phenyl)-3-[(R)-1-(3,3-dimethyl-2...)copy SMILEScopy InChI
Affinity DataIC50: 0.110nMAssay Description:Inhibitory concentration against radioligand [125I]-CCK-8 binding to gastrin/Cholecystokinin type B receptor from rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BBQPubMed
TargetGastrin/cholecystokinin type B receptor(RAT)
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50056092(1-(3-Diethylamino-phenyl)-3-[(R)-1-(3,3-dimethyl-2...)copy SMILEScopy InChI
Affinity DataIC50: 0.140nMAssay Description:Inhibitory concentration against radioligand [125I]-CCK-8 binding to gastrin/Cholecystokinin type B receptor from rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BBQPubMed
TargetGastrin/cholecystokinin type B receptor(RAT)
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50056091(1-[1-(3,3-Dimethyl-2-oxo-butyl)-2-oxo-5-phenyl-2,3...)copy SMILEScopy InChI
Affinity DataIC50: 0.160nMAssay Description:Inhibitory concentration against radioligand [125I]-CCK-8 binding to gastrin/Cholecystokinin type B receptor from rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BBQPubMed
TargetGastrin/cholecystokinin type B receptor(RAT)
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50056089(1-[(R)-1-(3,3-Dimethyl-2-oxo-butyl)-2-oxo-5-phenyl...)copy SMILEScopy InChI
Affinity DataIC50: 0.170nMAssay Description:Inhibitory concentration against radioligand [125I]-CCK-8 binding to gastrin/Cholecystokinin type B receptor from rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BBQPubMed
TargetGastrin/cholecystokinin type B receptor(RAT)
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50056095(1-(3-Dimethylamino-phenyl)-3-[(R)-1-(3,3-dimethyl-...)copy SMILEScopy InChI
Affinity DataIC50: 0.200nMAssay Description:Inhibitory concentration against radioligand [125I]-CCK-8 binding to gastrin/Cholecystokinin type B receptor from rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BBQPubMed
TargetGastrin/cholecystokinin type B receptor(RAT)
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50056098(1-(3-Dimethylamino-phenyl)-3-[(R)-1-(3,3-dimethyl-...)copy SMILEScopy InChI
Affinity DataIC50: 0.210nMAssay Description:Inhibitory concentration against radioligand [125I]-CCK-8 binding to gastrin/Cholecystokinin type B receptor from rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BBQPubMed
TargetGastrin/cholecystokinin type B receptor(RAT)
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50056086(1-(3-Amino-phenyl)-3-[(R)-1-(3,3-dimethyl-2-oxo-bu...)copy SMILEScopy InChI
Affinity DataIC50: 0.430nMAssay Description:Inhibitory concentration against radioligand [125I]-CCK-8 binding to gastrin/Cholecystokinin type B receptor from rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BBQPubMed
TargetGastrin/cholecystokinin type B receptor(RAT)
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50056096(1-[(R)-1-(3,3-Dimethyl-2-oxo-butyl)-2-oxo-5-pyridi...)copy SMILEScopy InChI
Affinity DataIC50: 0.440nMAssay Description:Inhibitory concentration against radioligand [125I]-CCK-8 binding to gastrin/Cholecystokinin type B receptor from rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BBQPubMed
TargetGastrin/cholecystokinin type B receptor(RAT)
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50056094(1-(3-Amino-phenyl)-3-[(R)-1-(3,3-dimethyl-2-oxo-bu...)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMAssay Description:Inhibitory concentration against radioligand [125I]-CCK-8 binding to gastrin/Cholecystokinin type B receptor from rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BBQPubMed
TargetGastrin/cholecystokinin type B receptor(RAT)
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50056097(1-[(R)-1-(3,3-Dimethyl-2-oxo-butyl)-2-oxo-5-phenyl...)copy SMILEScopy InChI
Affinity DataIC50: 0.520nMAssay Description:Inhibitory concentration against radioligand [125I]-CCK-8 binding to gastrin/Cholecystokinin type B receptor from rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BBQPubMed
TargetGastrin/cholecystokinin type B receptor(RAT)
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50056085(CHEMBL325746 | N-(3-{3-[1-(3,3-Dimethyl-2-oxo-buty...)copy SMILEScopy InChI
Affinity DataIC50: 0.590nMAssay Description:Inhibitory concentration against radioligand [125I]-CCK-8 binding to gastrin/Cholecystokinin type B receptor from rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BBQPubMed
TargetGastrin/cholecystokinin type B receptor(RAT)
Ferring Research Institute

Curated by ChEMBL
LigandPNGBDBM50056100(1-[(R)-1-(3,3-Dimethyl-2-oxo-butyl)-2-oxo-5-pyridi...)copy SMILEScopy InChI
Affinity DataIC50: 0.840nMAssay Description:Inhibitory concentration against radioligand [125I]-CCK-8 binding to gastrin/Cholecystokinin type B receptor from rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4BBQPubMed
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