Compile Data Set for Download or QSAR
Found 12 Enz. Inhib. hit(s) with all data for entry = 50046593
TargetTyrosinase(Homo sapiens (Human))
Tokyo University of Agriculture and Technology

Curated by ChEMBL
LigandPNGBDBM50292636(4-hexyl resorcinol | ACRISORCIN | CHEMBL443605)copy SMILEScopy InChI
Affinity DataIC50: 560nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DR2X9WPubMed
TargetTyrosinase(Homo sapiens (Human))
Tokyo University of Agriculture and Technology

Curated by ChEMBL
LigandPNGBDBM50120802(CHEMBL3100130)copy SMILEScopy InChI
Affinity DataIC50: 1.51E+3nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DR2X9WPubMed
TargetTyrosinase(Homo sapiens (Human))
Tokyo University of Agriculture and Technology

Curated by ChEMBL
LigandPNGBDBM50120803(CHEMBL3100134)copy SMILEScopy InChI
Affinity DataIC50: 1.72E+3nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DR2X9WPubMed
TargetTyrosinase(Homo sapiens (Human))
Tokyo University of Agriculture and Technology

Curated by ChEMBL
LigandPNGBDBM50120804(CHEMBL3618459)copy SMILEScopy InChI
Affinity DataIC50: 1.78E+3nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DR2X9WPubMed
TargetTyrosinase(Homo sapiens (Human))
Tokyo University of Agriculture and Technology

Curated by ChEMBL
LigandPNGBDBM50120800(CHEMBL3618460)copy SMILEScopy InChI
Affinity DataIC50: 1.98E+3nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DR2X9WPubMed
TargetTyrosinase(Homo sapiens (Human))
Tokyo University of Agriculture and Technology

Curated by ChEMBL
LigandPNGBDBM50120813(CHEMBL3618457)copy SMILEScopy InChI
Affinity DataIC50: 2.17E+3nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DR2X9WPubMed
TargetTyrosinase(Homo sapiens (Human))
Tokyo University of Agriculture and Technology

Curated by ChEMBL
LigandPNGBDBM50120806(CHEMBL3100132)copy SMILEScopy InChI
Affinity DataIC50: 2.30E+3nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DR2X9WPubMed
TargetTyrosinase(Homo sapiens (Human))
Tokyo University of Agriculture and Technology

Curated by ChEMBL
LigandPNGBDBM50120810(CHEMBL3100135)copy SMILEScopy InChI
Affinity DataIC50: 3.83E+3nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DR2X9WPubMed
TargetTyrosinase(Homo sapiens (Human))
Tokyo University of Agriculture and Technology

Curated by ChEMBL
LigandPNGBDBM50120807(CHEMBL3618458)copy SMILEScopy InChI
Affinity DataIC50: 4.13E+3nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DR2X9WPubMed
TargetTyrosinase(Homo sapiens (Human))
Tokyo University of Agriculture and Technology

Curated by ChEMBL
LigandPNGBDBM50120811(CHEMBL3100133)copy SMILEScopy InChI
Affinity DataIC50: 4.56E+3nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DR2X9WPubMed
TargetTyrosinase(Homo sapiens (Human))
Tokyo University of Agriculture and Technology

Curated by ChEMBL
LigandPNGBDBM50120814(CHEMBL3100131)copy SMILEScopy InChI
Affinity DataIC50: 4.72E+3nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DR2X9WPubMed
TargetTyrosinase(Homo sapiens (Human))
Tokyo University of Agriculture and Technology

Curated by ChEMBL
LigandPNGBDBM50031467(5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE | 5-Hyd...)copy SMILEScopy InChI
Affinity DataIC50: 9.15E+3nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate assessed as formation of dopachrome by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DR2X9WPubMed