Compile Data Set for Download or QSAR
Found 192 with Last Name = 'johns' and Initial = 'md'
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50222915(4'-[5-(4-pyrrolidin-1-ylmethyl-phenylamino)-1H-pyr...)copy SMILEScopy InChI
Affinity DataKi:  0.180nMAssay Description:Inhibition of human CHK1 expressed in baculovirus/insect cell systemMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K0754DPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50222916(4'-{5-[4-(dimethylamino-methyl)-phenylamino]-2H-py...)copy SMILEScopy InChI
Affinity DataKi:  0.190nMAssay Description:Inhibition of human CHK1 expressed in baculovirus/insect cell systemMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K0754DPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50222920(4'-{5-[6-(sec-butylamino-methyl)-pyridin-3-ylamino...)copy SMILEScopy InChI
Affinity DataKi:  0.200nMAssay Description:Inhibition of human CHK1 expressed in baculovirus/insect cell systemMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K0754DPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50222917(4'-[5-(6-piperidin-1-ylmethyl-pyridin-3-ylamino)-1...)copy SMILEScopy InChI
Affinity DataKi:  0.300nMAssay Description:Inhibition of human CHK1 expressed in baculovirus/insect cell systemMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K0754DPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50222913(4'-{5-[4-(isopropylamino-methyl)-phenylamino]-2H-p...)copy SMILEScopy InChI
Affinity DataKi:  0.360nMAssay Description:Inhibition of human CHK1 expressed in baculovirus/insect cell systemMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K0754DPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50222914(4'-[5-(4-cyclopropylaminomethyl-phenylamino)-2H-py...)copy SMILEScopy InChI
Affinity DataKi:  0.380nMAssay Description:Inhibition of human CHK1 expressed in baculovirus/insect cell systemMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K0754DPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50222921(3-(1H-benzo[d]imidazol-2-yl)-N-(2,4-dihydroxypheny...)copy SMILEScopy InChI
Affinity DataKi:  0.5nMAssay Description:Inhibition of human CHK1 expressed in baculovirus/insect cell systemMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K0754DPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50222919(4'-(5-{6-[(cyclopropylmethyl-amino)-methyl]-pyridi...)copy SMILEScopy InChI
Affinity DataKi:  0.800nMAssay Description:Inhibition of human CHK1 expressed in baculovirus/insect cell systemMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K0754DPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50222918(4'-(5-phenylamino-2H-pyrazol-3-yl)-biphenyl-2,4-di...)copy SMILEScopy InChI
Affinity DataKi:  1.20nMAssay Description:Inhibition of human CHK1 expressed in baculovirus/insect cell systemMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K0754DPubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Georgetown University Medical Center

LigandPNGBDBM21737(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  100nM ΔG°:  -39.6kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Georgetown University Medical Center

LigandPNGBDBM21751(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  160nM ΔG°:  -38.4kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50222922(3-(1H-benzo[d]imidazol-2-yl)-N-(4-hydroxyphenyl)-1...)copy SMILEScopy InChI
Affinity DataKi:  301nMAssay Description:Inhibition of human CHK1 expressed in baculovirus/insect cell systemMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K0754DPubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Georgetown University Medical Center

LigandPNGBDBM21750(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31S,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  380nM ΔG°:  -36.3kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Georgetown University Medical Center

LigandPNGBDBM21746(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  450nM ΔG°:  -35.9kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Georgetown University Medical Center

LigandPNGBDBM21749(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  857nM ΔG°:  -34.3kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetProthrombin(Bos taurus (Bovine))
Georgetown University Medical Center

LigandPNGBDBM21739(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  860nM ΔG°:  -34.3kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Georgetown University Medical Center

LigandPNGBDBM21748(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  890nM ΔG°:  -34.2kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Georgetown University Medical Center

LigandPNGBDBM21747(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  1.00E+3nM ΔG°:  -33.9kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Georgetown University Medical Center

LigandPNGBDBM21745(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  2.33E+3nM ΔG°:  -31.8kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Georgetown University Medical Center

LigandPNGBDBM21739(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  4.75E+3nM ΔG°:  -30.1kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetProthrombin(Bos taurus (Bovine))
Georgetown University Medical Center

LigandPNGBDBM21737(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  5.00E+3nM ΔG°:  -30.0kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetProthrombin(Bos taurus (Bovine))
Georgetown University Medical Center

LigandPNGBDBM21749(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  7.63E+3nM ΔG°:  -28.9kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetProthrombin(Bos taurus (Bovine))
Georgetown University Medical Center

LigandPNGBDBM21751(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  1.00E+4nM ΔG°:  -28.3kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetProthrombin(Bos taurus (Bovine))
Georgetown University Medical Center

LigandPNGBDBM21746(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  1.63E+4nM ΔG°:  -27.1kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Georgetown University Medical Center

LigandPNGBDBM21742(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  2.25E+4nM ΔG°:  -26.3kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetProthrombin(Bos taurus (Bovine))
Georgetown University Medical Center

LigandPNGBDBM21747(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  2.56E+4nM ΔG°:  -25.9kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Georgetown University Medical Center

LigandPNGBDBM21743(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  2.80E+4nM ΔG°:  -25.7kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetProthrombin(Bos taurus (Bovine))
Georgetown University Medical Center

LigandPNGBDBM21748(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  3.36E+4nM ΔG°:  -25.3kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetProthrombin(Bos taurus (Bovine))
Georgetown University Medical Center

LigandPNGBDBM21744(2-[(1S,7S,10S,13S,16S,22S,25S,31S,34S,37S,40S,43S,...)copy SMILEScopy InChI
Affinity DataKi:  4.04E+4nM ΔG°:  -24.8kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetProthrombin(Bos taurus (Bovine))
Georgetown University Medical Center

LigandPNGBDBM21743(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  4.56E+4nM ΔG°:  -24.5kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Georgetown University Medical Center

LigandPNGBDBM21741(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  9.00E+4nM ΔG°:  -22.9kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Georgetown University Medical Center

LigandPNGBDBM21744(2-[(1S,7S,10S,13S,16S,22S,25S,31S,34S,37S,40S,43S,...)copy SMILEScopy InChI
Affinity DataKi:  1.07E+5nM ΔG°:  -22.4kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetProthrombin(Bos taurus (Bovine))
Georgetown University Medical Center

LigandPNGBDBM21741(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  1.64E+5nM ΔG°:  -21.4kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Georgetown University Medical Center

LigandPNGBDBM21740(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi: >2.50E+5nM ΔG°: >-20.4kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetProthrombin(Bos taurus (Bovine))
Georgetown University Medical Center

LigandPNGBDBM21742(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi:  8.27E+5nM ΔG°:  -17.4kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetProthrombin(Bos taurus (Bovine))
Georgetown University Medical Center

LigandPNGBDBM21745(2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,4...)copy SMILEScopy InChI
Affinity DataKi: >2.50E+6nM ΔG°: >-14.7kJ/molepH: 8.5 T: 2°CAssay Description:The enzyme reaction was initiated by adding fluorescence peptide substrate to reaction mixture containing enzyme and test compounds. The enzyme activ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75DNJPubMed
TargetGlucagon receptor(Rattus norvegicus)
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50122102(3-Cyano-4-hydroxy-benzoic acid [1-(2,3,5,6-tetrame...)copy SMILEScopy InChI
Affinity DataIC50: 0.430nMAssay Description:In vitro binding affinity of the compound towards rat glucagon receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26W99FDPubMed
TargetGlucagon receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50122102(3-Cyano-4-hydroxy-benzoic acid [1-(2,3,5,6-tetrame...)copy SMILEScopy InChI
Affinity DataIC50: 2.30nMAssay Description:In vitro binding affinity for recombinant human glucagon receptor (hGGR) in BHK cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26W99FDPubMed
TargetGlucagon receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50122159(CHEMBL152477 | Cyclopentanecarboxylic acid {4-[(3-...)copy SMILEScopy InChI
Affinity DataIC50: 2.80nMAssay Description:In vitro binding affinity for recombinant human glucagon receptor (hGGR) in BHK cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26W99FDPubMed
TargetGlucagon receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50122153(CHEMBL156724 | Cyclopentanecarboxylic acid {4-[(3-...)copy SMILEScopy InChI
Affinity DataIC50: 3.40nMAssay Description:In vitro binding affinity for recombinant human glucagon receptor (hGGR) in BHK cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26W99FDPubMed
TargetGlucagon receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50110074(3-Chloro-4-hydroxy-benzoic acid [1-[4-(4-isopropyl...)copy SMILEScopy InChI
Affinity DataIC50: 4.30nMAssay Description:In vitro binding affinity for recombinant human glucagon receptor (hGGR) in BHK cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26W99FDPubMed
TargetGlucagon receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50122116(3-Chloro-4-hydroxy-benzoic acid (4-{2-[4-(4-chloro...)copy SMILEScopy InChI
Affinity DataIC50: 4.60nMAssay Description:In vitro binding affinity for recombinant human glucagon receptor (hGGR) in BHK cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26W99FDPubMed
TargetGlucagon receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50122160(3-Cyano-4-hydroxy-benzoic acid {4-[4-(4-chloro-ben...)copy SMILEScopy InChI
Affinity DataIC50: 4.90nMAssay Description:In vitro binding affinity for recombinant human glucagon receptor (hGGR) in BHK cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26W99FDPubMed
TargetGlucagon receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50122135(3-Chloro-4-hydroxy-benzoic acid [1-(2,3,5,6-tetram...)copy SMILEScopy InChI
Affinity DataIC50: 5.30nMAssay Description:In vitro binding affinity for recombinant human glucagon receptor (hGGR) in BHK cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26W99FDPubMed
TargetGlucagon receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50122142(3-Chloro-4-hydroxy-benzoic acid [1-(2,4,6-trimethy...)copy SMILEScopy InChI
Affinity DataIC50: 5.80nMAssay Description:In vitro binding affinity for recombinant human glucagon receptor (hGGR) in BHK cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26W99FDPubMed
TargetGlucagon receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50122152(4-[(3-Chloro-4-hydroxy-benzoyl)-hydrazonomethyl]-n...)copy SMILEScopy InChI
Affinity DataIC50: 5.90nMAssay Description:In vitro binding affinity for recombinant human glucagon receptor (hGGR) in BHK cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26W99FDPubMed
TargetGlucagon receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50122158(3-Cyano-4-hydroxy-benzoic acid (4-{2-[4-(4-bromo-p...)copy SMILEScopy InChI
Affinity DataIC50: 6.10nMAssay Description:In vitro binding affinity for recombinant human glucagon receptor (hGGR) in BHK cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26W99FDPubMed
TargetGlucagon receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50122125(CHEMBL421809 | N-Benzyl-2-{4-[(3-chloro-4-hydroxy-...)copy SMILEScopy InChI
Affinity DataIC50: 6.20nMAssay Description:In vitro binding affinity for recombinant human glucagon receptor (hGGR) in BHK cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26W99FDPubMed
TargetGlucagon receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50409681(CHEMBL2112908)copy SMILEScopy InChI
Affinity DataIC50: 6.40nMAssay Description:In vitro binding affinity for recombinant human glucagon receptor (hGGR) in BHK cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26W99FDPubMed
TargetGlucagon receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50122124(3-Chloro-4-hydroxy-benzoic acid (4-{2-[4-(4-bromo-...)copy SMILEScopy InChI
Affinity DataIC50: 6.60nMAssay Description:In vitro binding affinity for recombinant human glucagon receptor (hGGR) in BHK cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26W99FDPubMed
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