Compile Data Set for Download or QSAR
Found 114 with Last Name = 'kudo' and Initial = 't'
TargetHistamine H3 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM22542(4-(1H-imidazol-4-ylmethyl)piperidine | 4-(1H-imida...)copy SMILEScopy InChI
Affinity DataKi:  0.300nMAssay Description:Displacement of [3H]-(R)-alpha-methylhistamine from human histamine H3 receptor expressed in CHO cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50317865(2-(2-(4-tert-Butylphenylthio)ethyl)-1H-imidazole |...)copy SMILEScopy InChI
Affinity DataKi:  0.430nMAssay Description:Displacement of [3H]-(R)-alpha-methylhistamine from human histamine H3 receptor expressed in CHO cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM22910(4-(1H-imidazol-5-ylmethyl)pyridine | Immethridine)copy SMILEScopy InChI
Affinity DataKi:  0.770nMAssay Description:Displacement of [3H]-(R)-alpha-methylhistamine from human histamine H3 receptor expressed in CHO cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326285((S)-4-(1-(1H-Imidazol-4-yl)-2-(4-(trifluoromethyl)...)copy SMILEScopy InChI
Affinity DataKi:  14nMAssay Description:Displacement of [3H]-(R)-alpha-methylhistamine from human histamine H3 receptor expressed in CHO cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326287(2-(2-(4-tert-Butylphenylthio)-1-(1H-imidazol-4-yl)...)copy SMILEScopy InChI
Affinity DataKi:  16nMAssay Description:Displacement of [3H]-(R)-alpha-methylhistamine from human histamine H3 receptor expressed in CHO cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H4 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326289(4-(1-(1H-Imidazole-4-yl)-2-(4-trifluoromeethylphen...)copy SMILEScopy InChI
Affinity DataKi:  17nMAssay Description:Binding affinity to human histamine H4 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326286((R)-4-(1-(1H-Imidazol-4-yl)-2-(4-(trifluoromethyl)...)copy SMILEScopy InChI
Affinity DataKi:  18nMAssay Description:Displacement of [3H]-(R)-alpha-methylhistamine from human histamine H3 receptor expressed in CHO cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H1 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326286((R)-4-(1-(1H-Imidazol-4-yl)-2-(4-(trifluoromethyl)...)copy SMILEScopy InChI
Affinity DataKi:  48nMAssay Description:Binding affinity to human histamine H1 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326288(3-(2-(4-tert-Butylphenylthio)-1-(1H-imidazol-4-yl)...)copy SMILEScopy InChI
Affinity DataKi:  64nMAssay Description:Displacement of [3H]-(R)-alpha-methylhistamine from human histamine H3 receptor expressed in CHO cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326293(2-(1-(1H-Imidazole-4-yl)-2-(4-trifluoromeethylphen...)copy SMILEScopy InChI
Affinity DataKi:  75nMAssay Description:Displacement of [3H]-(R)-alpha-methylhistamine from human histamine H3 receptor expressed in CHO cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326297(3-((1H-imidazol-4-yl)methyl)pyridine | 3-(3H-Imida...)copy SMILEScopy InChI
Affinity DataKi:  76nMAssay Description:Displacement of [3H]-(R)-alpha-methylhistamine from human histamine H3 receptor expressed in CHO cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326294(3-(1-(1H-Imidazole-4-yl)-2-(4-trifluoromeethylphen...)copy SMILEScopy InChI
Affinity DataKi:  120nMAssay Description:Displacement of [3H]-(R)-alpha-methylhistamine from human histamine H3 receptor expressed in CHO cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326295(4-(2-(4-tert-Butylphenylthio)-1-(1H-imidazol-4-yl)...)copy SMILEScopy InChI
Affinity DataKi:  130nMAssay Description:Displacement of [3H]-(R)-alpha-methylhistamine from human histamine H3 receptor expressed in CHO cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326286((R)-4-(1-(1H-Imidazol-4-yl)-2-(4-(trifluoromethyl)...)copy SMILEScopy InChI
Affinity DataKi:  180nMAssay Description:Displacement of [3H]-(R)-alpha-methylhistamine from human histamine H3 receptor expressed in CHO cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326289(4-(1-(1H-Imidazole-4-yl)-2-(4-trifluoromeethylphen...)copy SMILEScopy InChI
Affinity DataKi:  200nMAssay Description:Displacement of [3H]-(R)-alpha-methylhistamine from human histamine H3 receptor expressed in CHO cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H1 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326285((S)-4-(1-(1H-Imidazol-4-yl)-2-(4-(trifluoromethyl)...)copy SMILEScopy InChI
Affinity DataKi:  280nMAssay Description:Binding affinity to human histamine H1 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H4 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326286((R)-4-(1-(1H-Imidazol-4-yl)-2-(4-(trifluoromethyl)...)copy SMILEScopy InChI
Affinity DataKi:  310nMAssay Description:Binding affinity to human histamine H4 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H4 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326288(3-(2-(4-tert-Butylphenylthio)-1-(1H-imidazol-4-yl)...)copy SMILEScopy InChI
Affinity DataKi:  360nMAssay Description:Binding affinity to human histamine H4 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326292(4-(2-(4-tert-Butylphenylthio)-1-(1H-imidazol-4-yl)...)copy SMILEScopy InChI
Affinity DataKi:  530nMAssay Description:Displacement of [3H]-(R)-alpha-methylhistamine from human histamine H3 receptor expressed in CHO cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H1 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326289(4-(1-(1H-Imidazole-4-yl)-2-(4-trifluoromeethylphen...)copy SMILEScopy InChI
Affinity DataKi:  540nMAssay Description:Binding affinity to human histamine H1 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H4 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326287(2-(2-(4-tert-Butylphenylthio)-1-(1H-imidazol-4-yl)...)copy SMILEScopy InChI
Affinity DataKi:  840nMAssay Description:Binding affinity to human histamine H4 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326291(3-(4-tert-Butylphenylthio)-2-(1H-imidazol-4-yl)-N-...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]-(R)-alpha-methylhistamine from human histamine H3 receptor expressed in CHO cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326290(2-(1H-Imidazol-4-yl)-N-methyl-3-(4-(trifluoromethy...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]-(R)-alpha-methylhistamine from human histamine H3 receptor expressed in CHO cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H4 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326285((S)-4-(1-(1H-Imidazol-4-yl)-2-(4-(trifluoromethyl)...)copy SMILEScopy InChI
Affinity DataKi:  1.30E+3nMAssay Description:Binding affinity to human histamine H4 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326296(2-((1H-imidazol-4-yl)methyl)pyridine | 2-(3H-Imida...)copy SMILEScopy InChI
Affinity DataKi:  1.80E+3nMAssay Description:Displacement of [3H]-(R)-alpha-methylhistamine from human histamine H3 receptor expressed in CHO cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H2 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326288(3-(2-(4-tert-Butylphenylthio)-1-(1H-imidazol-4-yl)...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity to human histamine H2 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H2 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326287(2-(2-(4-tert-Butylphenylthio)-1-(1H-imidazol-4-yl)...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity to human histamine H2 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H1 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326287(2-(2-(4-tert-Butylphenylthio)-1-(1H-imidazol-4-yl)...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity to human histamine H1 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H1 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326288(3-(2-(4-tert-Butylphenylthio)-1-(1H-imidazol-4-yl)...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity to human histamine H1 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H2 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326289(4-(1-(1H-Imidazole-4-yl)-2-(4-trifluoromeethylphen...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity to human histamine H2 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H2 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326286((R)-4-(1-(1H-Imidazol-4-yl)-2-(4-(trifluoromethyl)...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity to human histamine H2 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetHistamine H2 receptor(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326285((S)-4-(1-(1H-Imidazol-4-yl)-2-(4-(trifluoromethyl)...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity to human histamine H2 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetVitamin D3 receptor(Homo sapiens (Human))
Rikkyo University

Curated by ChEMBL
LigandPNGBDBM50015318(CHEMBL3263871)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMAssay Description:Displacement of [3H]-1,25(OH)2D3 from GST-fused human VDR-LBD expressed in Escherichia coli BL21More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZS2Z2GPubMed
TargetCytochrome P450 2C19(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50317865(2-(2-(4-tert-Butylphenylthio)ethyl)-1H-imidazole |...)copy SMILEScopy InChI
Affinity DataIC50: 8.5nMAssay Description:Inhibition of CYP2C19More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetVitamin D3 receptor(Homo sapiens (Human))
Rikkyo University

Curated by ChEMBL
LigandPNGBDBM50015316(CHEMBL3263873)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Displacement of [3H]-1,25(OH)2D3 from GST-fused human VDR-LBD expressed in Escherichia coli BL21More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZS2Z2GPubMed
TargetVitamin D3 receptor(Homo sapiens (Human))
Rikkyo University

Curated by ChEMBL
LigandPNGBDBM50015315(CHEMBL3263870)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Displacement of [3H]-1,25(OH)2D3 from GST-fused human VDR-LBD expressed in Escherichia coli BL21More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZS2Z2GPubMed
TargetVitamin D3 receptor(Homo sapiens (Human))
Rikkyo University

Curated by ChEMBL
LigandPNGBDBM50015317(CHEMBL3263872)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay Description:Displacement of [3H]-1,25(OH)2D3 from GST-fused human VDR-LBD expressed in Escherichia coli BL21More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZS2Z2GPubMed
TargetCytochrome P450 2C19(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326289(4-(1-(1H-Imidazole-4-yl)-2-(4-trifluoromeethylphen...)copy SMILEScopy InChI
Affinity DataIC50: 55nMAssay Description:Inhibition of CYP2C19More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326287(2-(2-(4-tert-Butylphenylthio)-1-(1H-imidazol-4-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 270nMAssay Description:Inhibition of CYP3A4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326289(4-(1-(1H-Imidazole-4-yl)-2-(4-trifluoromeethylphen...)copy SMILEScopy InChI
Affinity DataIC50: 350nMAssay Description:Inhibition of CYP3A4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50317865(2-(2-(4-tert-Butylphenylthio)ethyl)-1H-imidazole |...)copy SMILEScopy InChI
Affinity DataIC50: 470nMAssay Description:Inhibition of CYP3A4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetCytochrome P450 1A2(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50317865(2-(2-(4-tert-Butylphenylthio)ethyl)-1H-imidazole |...)copy SMILEScopy InChI
Affinity DataIC50: 680nMAssay Description:Inhibition of CYP1A2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50317865(2-(2-(4-tert-Butylphenylthio)ethyl)-1H-imidazole |...)copy SMILEScopy InChI
Affinity DataIC50: 680nMAssay Description:Inhibition of CYP2D6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326287(2-(2-(4-tert-Butylphenylthio)-1-(1H-imidazol-4-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 820nMAssay Description:Inhibition of CYP2D6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetCytochrome P450 2C19(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326292(4-(2-(4-tert-Butylphenylthio)-1-(1H-imidazol-4-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibition of CYP2C19More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetMetallo-beta-lactamase IMP-1(Pseudomonas aeruginosa)
Meiji Seika Pharma, Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50493102(CHEMBL566579)copy SMILEScopy InChI
Affinity DataIC50: 1.55E+3nMAssay Description:Inhibition of carbapenems-resistant Pseudomonas aeruginosa MSC15369 metallo-beta-lactamase IMP1 expressed in Escherichia coli DH5[alpha] using nitroc...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24X5BQMPubMed
TargetMetallo-beta-lactamase IMP-1(Pseudomonas aeruginosa)
Meiji Seika Pharma, Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50493088(CHEMBL2420935)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibition of carbapenems-resistant Pseudomonas aeruginosa MSC15369 metallo-beta-lactamase IMP1 expressed in Escherichia coli DH5[alpha] using nitroc...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24X5BQMPubMed
TargetMetallo-beta-lactamase IMP-1(Pseudomonas aeruginosa)
Meiji Seika Pharma, Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50493103(CHEMBL2420934)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of carbapenems-resistant Pseudomonas aeruginosa MSC15369 metallo-beta-lactamase IMP1 expressed in Escherichia coli DH5[alpha] using nitroc...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24X5BQMPubMed
TargetMetallo-beta-lactamase IMP-1(Pseudomonas aeruginosa)
Meiji Seika Pharma, Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50493084(CHEMBL2420944)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of carbapenems-resistant Pseudomonas aeruginosa MSC15369 metallo-beta-lactamase IMP1 expressed in Escherichia coli DH5[alpha] using nitroc...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24X5BQMPubMed
TargetMetallo-beta-lactamase IMP-1(Pseudomonas aeruginosa)
Meiji Seika Pharma, Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50493083(CHEMBL2420948)copy SMILEScopy InChI
Affinity DataIC50: 2.30E+3nMAssay Description:Inhibition of carbapenems-resistant Pseudomonas aeruginosa MSC15369 metallo-beta-lactamase IMP1 expressed in Escherichia coli DH5[alpha] using nitroc...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24X5BQMPubMed
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