Compile Data Set for Download or QSAR
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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
TargetMetallo-beta-lactamase IMP-1(Pseudomonas aeruginosa)
Meiji Seika Pharma, Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50493095(CHEMBL2420946)copy SMILEScopy InChI
Affinity DataIC50: 2.60E+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
LigandPNGBDBM50493082(CHEMBL2420945)copy SMILEScopy InChI
Affinity DataIC50: 2.70E+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 sidPDB
TargetMetallo-beta-lactamase IMP-1(Pseudomonas aeruginosa)
Meiji Seika Pharma, Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50493097(CHEMBL2420943)copy SMILEScopy InChI
Affinity DataIC50: 2.70E+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
LigandPNGBDBM50493093(CHEMBL2420941)copy SMILEScopy InChI
Affinity DataIC50: 2.80E+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
TargetCytochrome P450 2D6(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: 3.60E+3nMAssay Description:Inhibition of CYP2D6More 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
LigandPNGBDBM50493101(CHEMBL2420949)copy SMILEScopy InChI
Affinity DataIC50: 3.70E+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
TargetCytochrome P450 2D6(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: 4.30E+3nMAssay Description:Inhibition of CYP2D6More 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
LigandPNGBDBM50326287(2-(2-(4-tert-Butylphenylthio)-1-(1H-imidazol-4-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 5.10E+3nMAssay Description:Inhibition of CYP1A2More 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
LigandPNGBDBM50493090(CHEMBL2420933)copy SMILEScopy InChI
Affinity DataIC50: 5.10E+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
TargetCytochrome P450 3A4(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: 6.50E+3nMAssay Description:Inhibition of CYP3A4More 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
LigandPNGBDBM50493091(CHEMBL2420932)copy SMILEScopy InChI
Affinity DataIC50: 7.40E+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
TargetCytochrome P450 1A2(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: 8.60E+3nMAssay 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
LigandPNGBDBM50326286((R)-4-(1-(1H-Imidazol-4-yl)-2-(4-(trifluoromethyl)...)copy SMILEScopy InChI
Affinity DataIC50: 9.50E+3nMAssay Description:Inhibition of CYP2D6More 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
LigandPNGBDBM50493100(CHEMBL2420942)copy SMILEScopy InChI
Affinity DataIC50: 1.08E+4nMAssay 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
TargetCytochrome P450 2C19(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 DataIC50: 1.20E+4nMAssay 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
LigandPNGBDBM50493086(CHEMBL2420939)copy SMILEScopy InChI
Affinity DataIC50: 1.31E+4nMAssay 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
TargetCytochrome P450 3A4(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 DataIC50: 1.70E+4nMAssay Description:Inhibition of CYP3A4More 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
LigandPNGBDBM50493087(CHEMBL2420936)copy SMILEScopy InChI
Affinity DataIC50: 1.88E+4nMAssay 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
LigandPNGBDBM50493098(CHEMBL2420938)copy SMILEScopy InChI
Affinity DataIC50: 2.14E+4nMAssay 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
LigandPNGBDBM50493096(CHEMBL2420947)copy SMILEScopy InChI
Affinity DataIC50: 2.56E+4nMAssay 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
LigandPNGBDBM50493092(CHEMBL2420937)copy SMILEScopy InChI
Affinity DataIC50: 4.78E+4nMAssay 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
TargetCytochrome P450 1A2(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 DataIC50: 9.40E+4nMAssay Description:Inhibition of CYP1A2More 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
LigandPNGBDBM50493085(CHEMBL2420940)copy SMILEScopy InChI
Affinity DataIC50: 9.45E+4nMAssay 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
TargetCytochrome P450 1A2(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: 1.00E+5nMAssay Description:Inhibition of CYP1A2More 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
LigandPNGBDBM50493094(CHEMBL2420931)copy SMILEScopy InChI
Affinity DataIC50: 1.42E+5nMAssay 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
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24X5BQMPubMed
TargetMetallo-beta-lactamase IMP-1(Pseudomonas aeruginosa)
Meiji Seika Pharma, Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50493089(CHEMBL2420929)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+5nMAssay 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
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24X5BQMPubMed
TargetMetallo-beta-lactamase IMP-1(Pseudomonas aeruginosa)
Meiji Seika Pharma, Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50493099(CHEMBL2420930)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+5nMAssay 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
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24X5BQMPubMed