Compile Data Set for Download or QSAR
Found 82 with Last Name = 'gregory' and Initial = 'js'
TargetCalpain small subunit 1/1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286446(CHEMBL341222 | {(S)-1-[(S)-1-(4-Hydroxy-benzyl)-2-...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibition of Calpain 1 by [3H]-acetyl-casein assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ03R1
TargetCalpain small subunit 1/1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286452(CHEMBL340020 | {(S)-1-[(S)-1-(4-Hydroxy-benzyl)-2-...)copy SMILEScopy InChI
Affinity DataIC50: 25nMAssay Description:Inhibition of Calpain 1 by [3H]-acetyl-casein assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ03R1
TargetCalpain small subunit 1/1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286449(CHEMBL338859 | {(S)-1-[(S)-1-(4-Methoxy-benzyl)-2-...)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibition of Calpain 1 by [3H]-acetyl-casein assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ03R1
TargetCalpain small subunit 1/1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50137397(CHEMBL341014 | [(S)-1-((S)-1-Benzyl-2-oxo-ethylcar...)copy SMILEScopy InChI
Affinity DataIC50: 35nMAssay Description:Inhibition of Calpain 1 by [3H]-acetyl-casein assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ03R1
TargetCalpain small subunit 1/1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50014577(CHEMBL286722 | MDL-2170 | Z-Val-Phe-H | [(S)-1-((S...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibition of Calpain 1 by [3H]-acetyl-casein assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ03R1
TargetCalpain small subunit 1/1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50073850((S)-2-((S)-2-Benzyloxycarbonylamino-3-methyl-butyr...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibition of Calpain 1 by [3H]-acetyl-casein assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ03R1
TargetCalpain small subunit 1/1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286453(CHEMBL419423 | {(S)-1-[(S)-1-(4-Hydroxy-benzyl)-2-...)copy SMILEScopy InChI
Affinity DataIC50: 55nMAssay Description:Inhibition of Calpain 1 by [3H]-acetyl-casein assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ03R1
TargetCalpain small subunit 1/1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286455(CHEMBL128775 | [(S)-1-((S)-1-Benzyl-2-oxo-ethylcar...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of Calpain 1 by [3H]-acetyl-casein assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ03R1
TargetCalpain small subunit 1/1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286454(CHEMBL129657 | [(S)-1-((S)-1-Formyl-2-naphthalen-1...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of Calpain 1 by [3H]-acetyl-casein assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ03R1
TargetCalpain small subunit 1/1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286444(CHEMBL339000 | [(S)-1-((S)-1-Formyl-3-phenyl-propy...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of Calpain 1 by [3H]-acetyl-casein assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ03R1
TargetCalpain small subunit 1/1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286445(CHEMBL127613 | [((S)-1-Benzyl-2-oxo-ethylcarbamoyl...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of Calpain 1 by [3H]-acetyl-casein assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ03R1
TargetCalpain small subunit 1/1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286443(CHEMBL128776 | [(S)-1-((S)-1-Benzyl-2-oxo-ethylcar...)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Inhibition of Calpain 1 by [3H]-acetyl-casein assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ03R1
TargetCalpain small subunit 1/1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286456(CHEMBL129458 | [(S)-1-((S)-1-Benzyl-2-oxo-ethylcar...)copy SMILEScopy InChI
Affinity DataIC50: 270nMAssay Description:Inhibition of Calpain 1 by [3H]-acetyl-casein assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ03R1
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50213272(CHEBI:6426 | Leupeptin)copy SMILEScopy InChI
Affinity DataIC50: 300nMAssay Description:In vitro inhibitory activity against human erythrocyte Calpain 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCalpain small subunit 1/1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286450(CHEMBL128135 | [(S)-1-((S)-1-Benzyl-2-oxo-ethylcar...)copy SMILEScopy InChI
Affinity DataIC50: 400nMAssay Description:Inhibition of Calpain 1 by [3H]-acetyl-casein assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ03R1
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286432(1-(4-Hydroxy-2-methyl-phenyl)-4-oxo-7-pyridin-4-yl...)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:In vitro inhibitory activity against human erythrocyte Calpain 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCalpain small subunit 1/1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286451(CHEMBL129823 | [1-((S)-1-Benzyl-2-oxo-ethylcarbamo...)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:Inhibition of Calpain 1 by [3H]-acetyl-casein assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ03R1
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286434(1-(2-Chloro-4-hydroxy-phenyl)-4-oxo-7-pyridin-4-yl...)copy SMILEScopy InChI
Affinity DataIC50: 600nMAssay Description:In vitro inhibitory activity against human erythrocyte Calpain 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286442(1-(2-Chloro-4-hydroxy-phenyl)-4-oxo-7-pyrazol-1-yl...)copy SMILEScopy InChI
Affinity DataIC50: 600nMAssay Description:In vitro inhibitory activity against human erythrocyte Calpain 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286434(1-(2-Chloro-4-hydroxy-phenyl)-4-oxo-7-pyridin-4-yl...)copy SMILEScopy InChI
Affinity DataIC50: 600nMAssay Description:In vitro inhibitory activity against human erythrocyte Calpain 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCalpain small subunit 1/1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286447(CHEMBL2370670 | [1-(2-Formyl-pyrrolidine-1-carbony...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of Calpain 1 by [3H]-acetyl-casein assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ03R1
TargetCalpain small subunit 1/1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286448(CHEMBL127663 | [(S)-1-((S)-1-Benzyl-2-oxo-ethylcar...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of Calpain 1 by [3H]-acetyl-casein assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ03R1
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286440(1-(2-Chloro-4-hydroxy-phenyl)-7-furan-3-yl-4-oxo-1...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:In vitro inhibitory activity against human erythrocyte Calpain 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286426(1-(2-Chloro-4-hydroxy-phenyl)-7-(3-chloro-pyridin-...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:In vitro inhibitory activity against human erythrocyte Calpain 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286430(1-(4-Hydroxy-phenyl)-4-oxo-7-pyridin-4-yl-1,4-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:In vitro inhibitory activity against human erythrocyte Calpain 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286429(1-(2-Chloro-4-hydroxy-phenyl)-4-oxo-7-pyridazin-3-...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:In vitro inhibitory activity against human erythrocyte Calpain 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286436(1-(3-Chloro-4-hydroxy-phenyl)-4-oxo-7-pyridin-4-yl...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:In vitro inhibitory activity against human erythrocyte Calpain 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286437(1-(3-Fluoro-4-hydroxy-phenyl)-4-oxo-7-pyridin-4-yl...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:In vitro inhibitory activity against human erythrocyte Calpain 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286435(1-(3,4-Dihydroxy-phenyl)-4-oxo-7-pyridin-4-yl-1,4-...)copy SMILEScopy InChI
Affinity DataIC50: 7.00E+3nMAssay Description:In vitro inhibitory activity against human erythrocyte Calpain 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286433(1-(2-Fluoro-4-hydroxy-phenyl)-4-oxo-7-pyridin-4-yl...)copy SMILEScopy InChI
Affinity DataIC50: 7.00E+3nMAssay Description:In vitro inhibitory activity against human erythrocyte Calpain 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286439(1-(2-Chloro-4-hydroxy-phenyl)-4-oxo-7-pyridin-3-yl...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:In vitro inhibitory activity against human erythrocyte Calpain 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286438(1-(4-Hydroxy-2-trifluoromethyl-phenyl)-4-oxo-7-pyr...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:In vitro inhibitory activity against human erythrocyte Calpain 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286431(1-(4-Hydroxy-phenyl)-4-oxo-7-pyridin-4-yl-1,4-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:In vitro inhibitory activity against human erythrocyte Calpain 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetProcathepsin L(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286434(1-(2-Chloro-4-hydroxy-phenyl)-4-oxo-7-pyridin-4-yl...)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+4nMAssay Description:In vitro inhibitory activity against cathepsin LMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCathepsin B(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286434(1-(2-Chloro-4-hydroxy-phenyl)-4-oxo-7-pyridin-4-yl...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+4nMAssay Description:In vitro inhibitory activity against Cathepsin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286427(1-(2-Chloro-4-hydroxy-phenyl)-7-(2-fluoro-pyridin-...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:In vitro inhibitory activity against human erythrocyte Calpain 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286428(1-(2-Chloro-4-hydroxy-phenyl)-4-oxo-7-pyridin-2-yl...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:In vitro inhibitory activity against human erythrocyte Calpain 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCathepsin B(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286430(1-(4-Hydroxy-phenyl)-4-oxo-7-pyridin-4-yl-1,4-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 3.20E+4nMAssay Description:In vitro inhibitory activity against Cathepsin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetProcathepsin L(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286430(1-(4-Hydroxy-phenyl)-4-oxo-7-pyridin-4-yl-1,4-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 3.70E+4nMAssay Description:In vitro inhibitory activity against cathepsin LMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0M6W
TargetCystic fibrosis transmembrane conductance regulator(Homo sapiens (Human))
Genzyme Corp.

Curated by ChEMBL
LigandPNGBDBM50164966((R)-2-(3-Phenoxy-benzoyl)-1,2,3,4-tetrahydro-isoqu...)copy SMILEScopy InChI
Affinity DataEC50:  314nMAssay Description:Effective concentration for cellular chloride transport in C127 mouse epithelial cell transfected with recombinant Delta F508 CFTRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965WPPubMed
TargetCystic fibrosis transmembrane conductance regulator(Homo sapiens (Human))
Genzyme Corp.

Curated by ChEMBL
LigandPNGBDBM50164965((S)-2-(3-Isopropoxy-benzoyl)-1,2,3,4-tetrahydro-is...)copy SMILEScopy InChI
Affinity DataEC50:  6.30nMAssay Description:Effective concentration for cellular chloride transport in C127 mouse epithelial cell transfected with recombinant Delta F508 CFTRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965WPPubMed
TargetCystic fibrosis transmembrane conductance regulator(Homo sapiens (Human))
Genzyme Corp.

Curated by ChEMBL
LigandPNGBDBM50164968((S)-2-(3-Cyclohexyloxy-benzoyl)-1,2,3,4-tetrahydro...)copy SMILEScopy InChI
Affinity DataEC50:  20nMAssay Description:Effective concentration for cellular chloride transport in C127 mouse epithelial cell transfected with recombinant Delta F508 CFTRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965WPPubMed
TargetCystic fibrosis transmembrane conductance regulator(Homo sapiens (Human))
Genzyme Corp.

Curated by ChEMBL
LigandPNGBDBM50164967((R)-2-(3-Phenoxy-benzoyl)-1,2,3,4-tetrahydro-isoqu...)copy SMILEScopy InChI
Affinity DataEC50:  292nMAssay Description:Effective concentration for cellular chloride transport in C127 mouse epithelial cell transfected with recombinant Delta F508 CFTRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965WPPubMed
TargetCystic fibrosis transmembrane conductance regulator(Homo sapiens (Human))
Genzyme Corp.

Curated by ChEMBL
LigandPNGBDBM50164969((S)-2-(3-Methoxy-benzoyl)-1,2,3,4-tetrahydro-isoqu...)copy SMILEScopy InChI
Affinity DataEC50:  176nMAssay Description:Effective concentration for cellular chloride transport in C127 mouse epithelial cell transfected with recombinant Delta F508 CFTRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965WPPubMed
TargetCystic fibrosis transmembrane conductance regulator(Homo sapiens (Human))
Genzyme Corp.

Curated by ChEMBL
LigandPNGBDBM50164970((R)-2-[3-(Pyridin-2-yloxy)-benzoyl]-1,2,3,4-tetrah...)copy SMILEScopy InChI
Affinity DataEC50:  268nMAssay Description:Effective concentration for cellular chloride transport in C127 mouse epithelial cell transfected with recombinant Delta F508 CFTRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965WPPubMed
TargetCystic fibrosis transmembrane conductance regulator(Homo sapiens (Human))
Genzyme Corp.

Curated by ChEMBL
LigandPNGBDBM50164971((R)-2-(3-Phenoxy-benzoyl)-1,2,3,4-tetrahydro-isoqu...)copy SMILEScopy InChI
Affinity DataEC50:  145nMAssay Description:Effective concentration for cellular chloride transport in C127 mouse epithelial cell transfected with recombinant Delta F508 CFTRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965WPPubMed
TargetCystic fibrosis transmembrane conductance regulator(Homo sapiens (Human))
Genzyme Corp.

Curated by ChEMBL
LigandPNGBDBM50164972((R)-2-(3-Benzyl-benzoyl)-1,2,3,4-tetrahydro-isoqui...)copy SMILEScopy InChI
Affinity DataEC50:  291nMAssay Description:Effective concentration for cellular chloride transport in C127 mouse epithelial cell transfected with recombinant Delta F508 CFTRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965WPPubMed
TargetCystic fibrosis transmembrane conductance regulator(Homo sapiens (Human))
Genzyme Corp.

Curated by ChEMBL
LigandPNGBDBM50164973((R)-2-[3-(4-Fluoro-phenoxy)-benzoyl]-1,2,3,4-tetra...)copy SMILEScopy InChI
Affinity DataEC50:  590nMAssay Description:Effective concentration for cellular chloride transport in C127 mouse epithelial cell transfected with recombinant Delta F508 CFTRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965WPPubMed
TargetCystic fibrosis transmembrane conductance regulator(Homo sapiens (Human))
Genzyme Corp.

Curated by ChEMBL
LigandPNGBDBM50164974((S)-2-(3,4-Dichloro-benzoyl)-1,2,3,4-tetrahydro-is...)copy SMILEScopy InChI
Affinity DataEC50:  82nMAssay Description:Effective concentration for cellular chloride transport in C127 mouse epithelial cell transfected with recombinant Delta F508 CFTRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965WPPubMed
TargetCystic fibrosis transmembrane conductance regulator(Homo sapiens (Human))
Genzyme Corp.

Curated by ChEMBL
LigandPNGBDBM50164975((R)-2-(3-Phenoxy-benzoyl)-1,2,3,4-tetrahydro-isoqu...)copy SMILEScopy InChI
Affinity DataEC50:  230nMAssay Description:Effective concentration for cellular chloride transport in C127 mouse epithelial cell transfected with recombinant Delta F508 CFTRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965WPPubMed
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