Compile Data Set for Download or QSAR
Found 55 with Last Name = 'patterson' and Initial = 'aw'
TargetCathepsin S(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19484(1, 2, 3 -Triazole Nitrile Inhibitor, 11e | N-[(1S)...)copy SMILEScopy InChI
Affinity DataKi:  15nM ΔG°:  -46.5kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetCathepsin S(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19483(1, 2, 3 -Triazole Nitrile Inhibitor, 11d | N-[(1S)...)copy SMILEScopy InChI
Affinity DataKi:  18nM ΔG°:  -46.0kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetCathepsin S(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19482(1, 2, 3 -Triazole Nitrile Inhibitor, 11c | N-[(1S)...)copy SMILEScopy InChI
Affinity DataKi:  200nM ΔG°:  -39.8kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetCathepsin S(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19481(1, 2, 3 -Triazole Nitrile Inhibitor, 11b | N-[(2S)...)copy SMILEScopy InChI
Affinity DataKi:  420nM ΔG°:  -37.9kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetCathepsin K(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19481(1, 2, 3 -Triazole Nitrile Inhibitor, 11b | N-[(2S)...)copy SMILEScopy InChI
Affinity DataKi:  430nM ΔG°:  -37.8kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetCathepsin K(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19479(1, 2, 3 -Triazole Nitrile Inhibitor, 11a | N-[(2S)...)copy SMILEScopy InChI
Affinity DataKi:  880nM ΔG°:  -36.0kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetCathepsin S(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19479(1, 2, 3 -Triazole Nitrile Inhibitor, 11a | N-[(2S)...)copy SMILEScopy InChI
Affinity DataKi:  1.20E+3nM ΔG°:  -35.2kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetCathepsin K(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19483(1, 2, 3 -Triazole Nitrile Inhibitor, 11d | N-[(1S)...)copy SMILEScopy InChI
Affinity DataKi:  1.70E+3nM ΔG°:  -34.3kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetCathepsin K(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19482(1, 2, 3 -Triazole Nitrile Inhibitor, 11c | N-[(1S)...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nM ΔG°: >-29.7kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetProcathepsin L(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19483(1, 2, 3 -Triazole Nitrile Inhibitor, 11d | N-[(1S)...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nM ΔG°: >-29.7kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetProcathepsin L(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19482(1, 2, 3 -Triazole Nitrile Inhibitor, 11c | N-[(1S)...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nM ΔG°: >-29.7kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetProcathepsin L(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19481(1, 2, 3 -Triazole Nitrile Inhibitor, 11b | N-[(2S)...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nM ΔG°: >-29.7kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetProcathepsin L(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19479(1, 2, 3 -Triazole Nitrile Inhibitor, 11a | N-[(2S)...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nM ΔG°: >-29.7kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetCathepsin B(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19481(1, 2, 3 -Triazole Nitrile Inhibitor, 11b | N-[(2S)...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nM ΔG°: >-29.7kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetCathepsin B(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19483(1, 2, 3 -Triazole Nitrile Inhibitor, 11d | N-[(1S)...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nM ΔG°: >-29.7kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetCathepsin B(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19482(1, 2, 3 -Triazole Nitrile Inhibitor, 11c | N-[(1S)...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nM ΔG°: >-29.7kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetCathepsin B(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19479(1, 2, 3 -Triazole Nitrile Inhibitor, 11a | N-[(2S)...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nM ΔG°: >-29.7kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetProcathepsin L(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19484(1, 2, 3 -Triazole Nitrile Inhibitor, 11e | N-[(1S)...)copy SMILEScopy InChI
Affinity DataKi: >1.50E+4nM ΔG°: >-28.6kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetCathepsin K(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19484(1, 2, 3 -Triazole Nitrile Inhibitor, 11e | N-[(1S)...)copy SMILEScopy InChI
Affinity DataKi: >1.50E+4nM ΔG°: >-28.6kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetCathepsin B(Homo sapiens (Human))
University of California at Berkeley

LigandPNGBDBM19484(1, 2, 3 -Triazole Nitrile Inhibitor, 11e | N-[(1S)...)copy SMILEScopy InChI
Affinity DataKi: >1.50E+4nM ΔG°: >-28.6kJ/molepH: 6.1 T: 2°CAssay Description:The proteolytic cleavage of N-acyl aminocoumarins by cathepsins was conducted in Dynatech Microfluor fluorescence 96-well microtiter plates, and read...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0RSVPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543851(CHEMBL4641455)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibition of myeloperoxidase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543859(CHEMBL4637559)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Inhibition of myeloperoxidase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543850(CHEMBL4645343)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Inhibition of myeloperoxidase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543859(CHEMBL4637559)copy SMILEScopy InChI
Affinity DataIC50: 170nMAssay Description:Inhibition of human plasma myeloperoxidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543858(CHEMBL4632667)copy SMILEScopy InChI
Affinity DataIC50: 170nMAssay Description:Inhibition of myeloperoxidase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543849(CHEMBL4637728)copy SMILEScopy InChI
Affinity DataIC50: 220nMAssay Description:Inhibition of myeloperoxidase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543852(CHEMBL4633000)copy SMILEScopy InChI
Affinity DataIC50: 250nMAssay Description:Inhibition of myeloperoxidase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543854(CHEMBL4649237)copy SMILEScopy InChI
Affinity DataIC50: 330nMAssay Description:Inhibition of myeloperoxidase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543851(CHEMBL4641455)copy SMILEScopy InChI
Affinity DataIC50: 360nMAssay Description:Inhibition of human plasma myeloperoxidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543853(CHEMBL4641477)copy SMILEScopy InChI
Affinity DataIC50: 420nMAssay Description:Inhibition of myeloperoxidase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50503707(AZD-3241 | Azd 3241 | Azd3241 | BHV-3241 | BHV-342...)copy SMILEScopy InChI
Affinity DataIC50: 630nMAssay Description:Inhibition of myeloperoxidase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543854(CHEMBL4649237)copy SMILEScopy InChI
Affinity DataIC50: 900nMAssay Description:Inhibition of human plasma myeloperoxidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543850(CHEMBL4645343)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543854(CHEMBL4649237)copy SMILEScopy InChI
Affinity DataIC50: 1.90E+3nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543856(CHEMBL4639481)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of myeloperoxidase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543850(CHEMBL4645343)copy SMILEScopy InChI
Affinity DataIC50: 2.60E+3nMAssay Description:Inhibition of human plasma myeloperoxidaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543849(CHEMBL4637728)copy SMILEScopy InChI
Affinity DataIC50: 2.80E+3nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543851(CHEMBL4641455)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543855(CHEMBL4645782)copy SMILEScopy InChI
Affinity DataIC50: 4.20E+3nMAssay Description:Inhibition of myeloperoxidase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543857(CHEMBL4638616)copy SMILEScopy InChI
Affinity DataIC50: 5.20E+3nMAssay Description:Inhibition of myeloperoxidase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetThyroid peroxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543850(CHEMBL4645343)copy SMILEScopy InChI
Affinity DataIC50: 5.30E+3nMAssay Description:Inhibition of thyroid peroxidase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetThyroid peroxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543852(CHEMBL4633000)copy SMILEScopy InChI
Affinity DataIC50: 5.90E+3nMAssay Description:Inhibition of thyroid peroxidase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543859(CHEMBL4637559)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+4nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543853(CHEMBL4641477)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+4nMAssay Description:Inhibition of human plasma myeloperoxidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543852(CHEMBL4633000)copy SMILEScopy InChI
Affinity DataIC50: 2.30E+4nMAssay Description:Inhibition of human plasma myeloperoxidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetThyroid peroxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543858(CHEMBL4632667)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of thyroid peroxidase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetThyroid peroxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543859(CHEMBL4637559)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of thyroid peroxidase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetThyroid peroxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543853(CHEMBL4641477)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of thyroid peroxidase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetThyroid peroxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543854(CHEMBL4649237)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of thyroid peroxidase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
TargetThyroid peroxidase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50543849(CHEMBL4637728)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of thyroid peroxidase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668HRNPubMed
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