Compile Data Set for Download or QSAR
Found 51 with Last Name = 'nihei' and Initial = 'k'
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50263336(4,4'-(ethane-1,2-diyl)dibenzene-1,3-diol | CHEMBL4...)copy SMILEScopy InChI
Affinity DataIC50: 370nMAssay Description:Inhibition of TyrosinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8D41PubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50263336(4,4'-(ethane-1,2-diyl)dibenzene-1,3-diol | CHEMBL4...)copy SMILEScopy InChI
Affinity DataIC50: 370nMAssay Description:Inhibition of mushroom tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0GBZPubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50503718(CHEMBL4439507)copy SMILEScopy InChI
Affinity DataIC50: 390nMAssay Description:Inhibition of mushroom tyrosinase using TBC as substrate by spectrophotometric methodMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2KCKPubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50503713(CHEMBL4462064)copy SMILEScopy InChI
Affinity DataIC50: 410nMAssay Description:Inhibition of mushroom tyrosinase using TBC as substrate by spectrophotometric methodMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2KCKPubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50264086((2S,3R,4S,5R)-2-(4-(2,4-dihydroxyphenethyl)-3-hydr...)copy SMILEScopy InChI
Affinity DataIC50: 430nMAssay Description:Inhibition of mushroom tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0GBZPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50264086((2S,3R,4S,5R)-2-(4-(2,4-dihydroxyphenethyl)-3-hydr...)copy SMILEScopy InChI
Affinity DataIC50: 430nMAssay Description:Inhibition of TyrosinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8D41PubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50292636(4-hexyl resorcinol | ACRISORCIN | CHEMBL443605)copy SMILEScopy InChI
Affinity DataIC50: 560nMAssay Description:Inhibition of mushroom tyrosinase using L-DOPA as substrate assessed as dopachrome formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ8BMDPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

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
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50292636(4-hexyl resorcinol | ACRISORCIN | CHEMBL443605)copy SMILEScopy InChI
Affinity DataIC50: 610nMAssay Description:Inhibition of mushroom tyrosinase using TBC as substrate by spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2KCKPubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50503714(CHEMBL4456030)copy SMILEScopy InChI
Affinity DataIC50: 630nMAssay Description:Inhibition of mushroom tyrosinase using TBC as substrate by spectrophotometric methodMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2KCKPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50340788(4-(beta-D-Cellobiopyranosyl)-2,2',4'-trihydroxybib...)copy SMILEScopy InChI
Affinity DataIC50: 680nMAssay Description:Inhibition of TyrosinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8D41PubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50264087((2S,2'S,3R,3'R,4S,4'S,5R,5'R)-2,2'-(4-(2,4-dihydro...)copy SMILEScopy InChI
Affinity DataIC50: 730nMAssay Description:Inhibition of TyrosinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8D41PubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50264087((2S,2'S,3R,3'R,4S,4'S,5R,5'R)-2,2'-(4-(2,4-dihydro...)copy SMILEScopy InChI
Affinity DataIC50: 730nMAssay Description:Inhibition of mushroom tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0GBZPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50340787(4-(beta-D-Glucopyranosyl)-2,2',4'-trihydroxybibenz...)copy SMILEScopy InChI
Affinity DataIC50: 770nMAssay Description:Inhibition of TyrosinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8D41PubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50340789(2,2',4'-Trihydroxy-4-(beta-D-maltopyranosyl)bibenz...)copy SMILEScopy InChI
Affinity DataIC50: 830nMAssay Description:Inhibition of TyrosinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8D41PubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50503717(CHEMBL4465094)copy SMILEScopy InChI
Affinity DataIC50: 1.36E+3nMAssay Description:Inhibition of mushroom tyrosinase using TBC as substrate by spectrophotometric methodMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2KCKPubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50120802(CHEMBL3100130)copy SMILEScopy InChI
Affinity DataIC50: 1.51E+3nMAssay Description:Inhibition of mushroom tyrosinase using L-DOPA as substrate assessed as dopachrome formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ8BMDPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

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))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50264085((2S,3R,4S,5R)-2-(2-(2,4-dihydroxyphenethyl)-5-hydr...)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of TyrosinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8D41PubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50264085((2S,3R,4S,5R)-2-(2-(2,4-dihydroxyphenethyl)-5-hydr...)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of mushroom tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0GBZPubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50120803(CHEMBL3100134)copy SMILEScopy InChI
Affinity DataIC50: 1.72E+3nMAssay Description:Inhibition of mushroom tyrosinase using L-DOPA as substrate assessed as dopachrome formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ8BMDPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

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))
Utsunomiya University

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))
Utsunomiya University

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))
Utsunomiya University

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))
Utsunomiya University

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))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50139369(2-Hydroxy-4-isopropyl-benzaldehyde | CHEMBL353354)copy SMILEScopy InChI
Affinity DataIC50: 2.30E+3nMAssay Description:Inhibitory activity of the compound was evaluated against the oxidation of L-3,4-dihydroxyphenylalanine (L-DOPA) catalyzed by mushroom tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27S7N6XPubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50120806(CHEMBL3100132)copy SMILEScopy InChI
Affinity DataIC50: 2.30E+3nMAssay Description:Inhibition of mushroom tyrosinase using L-DOPA as substrate assessed as dopachrome formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ8BMDPubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50503712(CHEMBL4541503)copy SMILEScopy InChI
Affinity DataIC50: 3.62E+3nMAssay Description:Inhibition of mushroom tyrosinase using TBC as substrate by spectrophotometric methodMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2KCKPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

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
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50120810(CHEMBL3100135)copy SMILEScopy InChI
Affinity DataIC50: 3.83E+3nMAssay Description:Inhibition of mushroom tyrosinase using L-DOPA as substrate assessed as dopachrome formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ8BMDPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

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
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50120811(CHEMBL3100133)copy SMILEScopy InChI
Affinity DataIC50: 4.56E+3nMAssay Description:Inhibition of mushroom tyrosinase using L-DOPA as substrate assessed as dopachrome formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ8BMDPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

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
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50120814(CHEMBL3100131)copy SMILEScopy InChI
Affinity DataIC50: 4.72E+3nMAssay Description:Inhibition of mushroom tyrosinase using L-DOPA as substrate assessed as dopachrome formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ8BMDPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

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))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50031467(5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE | 5-Hyd...)copy SMILEScopy InChI
Affinity DataIC50: 7.40E+3nMAssay Description:Inhibition of TyrosinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8D41PubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50031467(5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE | 5-Hyd...)copy SMILEScopy InChI
Affinity DataIC50: 7.40E+3nMAssay Description:Inhibition of mushroom tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0GBZPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

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
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

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 mushroom tyrosinase using L-DOPA as substrate assessed as dopachrome formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ8BMDPubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50031467(5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE | 5-Hyd...)copy SMILEScopy InChI
Affinity DataIC50: 1.07E+4nMAssay Description:Inhibition of mushroom tyrosinase using TBC as substrate by spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2KCKPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50139368(2-Hydroxy-4-methoxy-benzaldehyde | 2-hydroxy-4-met...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibitory activity of the compound was evaluated against the oxidation of L-3,4-dihydroxyphenylalanine (L-DOPA) catalyzed by mushroom tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27S7N6XPubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50503716(CHEMBL4453823)copy SMILEScopy InChI
Affinity DataIC50: 3.59E+4nMAssay Description:Inhibition of mushroom tyrosinase using TBC as substrate by spectrophotometric methodMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2KCKPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50139366(4-Isopropyl-benzaldehyde | 4-isopropylbenzaldehyde...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibitory activity of the compound was evaluated against the oxidation of L-3,4-dihydroxyphenylalanine (L-DOPA) catalyzed by mushroom tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27S7N6XPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50031467(5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE | 5-Hyd...)copy SMILEScopy InChI
Affinity DataIC50: 2.80E+5nMAssay Description:Inhibitory activity against mushroom tyrosinase (approximate value given)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HD7W6HPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50139370(4-Methoxy-benzaldehyde | 4-methoxybenzaldehyde | C...)copy SMILEScopy InChI
Affinity DataIC50: 3.20E+5nMAssay Description:Inhibitory activity of the compound was evaluated against the oxidation of L-3,4-dihydroxyphenylalanine (L-DOPA) catalyzed by mushroom tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27S7N6XPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50503715(CHEMBL4586957)copy SMILEScopy InChI
Affinity DataIC50: 4.17E+5nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate preincubated with substrate for 5 mins followed by enzyme addition and measured i...More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22V2KCKPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM60953(BDBM50139371 | benzaldehyde)copy SMILEScopy InChI
Affinity DataIC50: 8.20E+5nMAssay Description:Inhibitory activity of the compound was evaluated against the oxidation of L-3,4-dihydroxyphenylalanine (L-DOPA) catalyzed by mushroom tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27S7N6XPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM50139367(2-hydroxybenzaldehyde | CHEMBL108925 | Salicylalde...)copy SMILEScopy InChI
Affinity DataIC50: 3.30E+6nMAssay Description:Inhibitory activity of the compound was evaluated against the oxidation of L-3,4-dihydroxyphenylalanine (L-DOPA) catalyzed by mushroom tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27S7N6XPubMed
TargetTyrosinase(Homo sapiens (Human))
Utsunomiya University

Curated by ChEMBL
LigandPNGBDBM60928(BDBM50130192 | L-3,4-dihydroxyphenylalanine | L-DO...)copy SMILEScopy InChI
Affinity DataIC50: 8.40E+6nMAssay Description:Inhibitory activity against mushroom tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HD7W6HPubMed
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