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Found 294 of ic50 data for polymerid = 5039
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50269559(2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4...)
Affinity DataIC50:  23nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-dihydroxyphenylalanine as substrate preincubated for 30 mins followed by substrate addition measure...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50287127((S)-2-(5-Hydroxy-4-oxo-4H-pyran-2-ylmethoxycarbony...)
Affinity DataIC50:  60nMAssay Description:Compound was evaluated for inhibition of tyrosinase enzyme.More data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50203985((E)-1-(2,4-dihydroxyphenyl)-3-(2,4-dihydroxyphenyl...)
Affinity DataIC50:  70nMAssay Description:Inhibition of tyrosinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50203985((E)-1-(2,4-dihydroxyphenyl)-3-(2,4-dihydroxyphenyl...)
Affinity DataIC50:  70nMAssay Description:Inhibition of tyrosinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50251013(2,4,2',4'-tetrahydroxy-3'-prenylchalcone | CHEMBL4...)
Affinity DataIC50:  80nMAssay Description:Inhibition of tyrosinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50251013(2,4,2',4'-tetrahydroxy-3'-prenylchalcone | CHEMBL4...)
Affinity DataIC50:  80nMAssay Description:Inhibition of tyrosinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50108046((oxyresveratrol)4-[(E)-2-(3,5-dihydroxyphenyl)viny...)
Affinity DataIC50:  90nMAssay Description:Inhibition of human tyrosinase expressed in HEK293 cells using L-tyrosine and DOPA as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50441626(GLABRIDIN | US9783551, Compound 1)
Affinity DataIC50:  90nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-tyrosine as substrate preincubated for 5 mins followed by substrate additionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50172095(CHEBI:69084 | Glyasperin D)
Affinity DataIC50:  154nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-tyrosine as substrate assessed as oxidation of L-tyrosine after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50529589(CHEMBL4239110)
Affinity DataIC50:  170nMAssay Description:Inhibition of tyrosinase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50529589(CHEMBL4239110)
Affinity DataIC50:  170nMAssay Description:Inhibition of tyrosinase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50172096(CHEBI:69089 | Glyasperin C)
Affinity DataIC50:  177nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-tyrosine as substrate assessed as oxidation of L-tyrosine after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50146416((S)-2-[(S)-2-[(S)-2-(5-Hydroxy-4-oxo-4H-pyran-2-yl...)
Affinity DataIC50:  240nMAssay Description:Inhibitory activity against mushroom tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50146418((S)-2-{(S)-2-[(S)-2-(5-Hydroxy-4-oxo-4H-pyran-2-yl...)
Affinity DataIC50:  330nMAssay Description:Inhibitory activity against mushroom tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50263336(4,4'-(ethane-1,2-diyl)dibenzene-1,3-diol | CHEMBL4...)
Affinity DataIC50:  370nMAssay Description:Inhibition of TyrosinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50146415((S)-2-[(S)-2-[(S)-2-(5-Hydroxy-4-oxo-4H-pyran-2-yl...)
Affinity DataIC50:  390nMAssay Description:Inhibitory activity against mushroom tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50264086((2S,3R,4S,5R)-2-(4-(2,4-dihydroxyphenethyl)-3-hydr...)
Affinity DataIC50:  430nMAssay Description:Inhibition of TyrosinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50292636(4-hexyl resorcinol | ACRISORCIN | CHEMBL443605)
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 ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50340788(4-(beta-D-Cellobiopyranosyl)-2,2',4'-trihydroxybib...)
Affinity DataIC50:  680nMAssay Description:Inhibition of TyrosinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50366430(CHEMBL1794031)
Affinity DataIC50:  700nMAssay Description:Compound was evaluated for inhibition of tyrosinase enzyme.More data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50264087((2S,2'S,3R,3'R,4S,4'S,5R,5'R)-2,2'-(4-(2,4-dihydro...)
Affinity DataIC50:  730nMAssay Description:Inhibition of TyrosinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50340787(4-(beta-D-Glucopyranosyl)-2,2',4'-trihydroxybibenz...)
Affinity DataIC50:  770nMAssay Description:Inhibition of TyrosinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50146414((2S)-2-[(2S)-2-[(2S)-2-({[(5-hydroxy-4-oxo-4H-pyra...)
Affinity DataIC50:  780nMAssay Description:Inhibitory activity against mushroom tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50340789(2,2',4'-Trihydroxy-4-(beta-D-maltopyranosyl)bibenz...)
Affinity DataIC50:  830nMAssay Description:Inhibition of TyrosinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50251005((2S)-5,7,2',4'-tetrahydroxyflavanone | (S)-2-(2,4-...)
Affinity DataIC50:  980nMAssay Description:Inhibition of tyrosinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50251005((2S)-5,7,2',4'-tetrahydroxyflavanone | (S)-2-(2,4-...)
Affinity DataIC50:  980nMAssay Description:Inhibition of tyrosinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50559077(CHEMBL4473314)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of tyrosinase in human neonatal foreskin epidermal melanocyte cells using L-tyrosine and L-DOPA as substrate preincubated for 2 days follo...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM7462(3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-tyrosine as substrate assessed as oxidation of L-tyrosine after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50559078(SUBAMOLIDE A)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of tyrosinase in human neonatal foreskin epidermal melanocyte cells using L-tyrosine and L-DOPA as substrate preincubated for 2 days follo...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50540075(CHEMBL2078992)
Affinity DataIC50:  1.07E+3nMAssay Description:Inhibition of tyrosinase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50559076(CHEMBL4743159)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibition of human His-tagged tyrosinase expressed in HEK 293 cells using L-DOPA as substrate by MBTH based assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50330795(2-hydroxy-5-isopropyl-2,4,6-cycloheptatrien-1-one ...)
Affinity DataIC50:  1.15E+3nMAssay Description:Competitive inhibition of tyrosinase in human G-361 cells incubated for 10 mins measured for 2 hrs by MBTH-based spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50330795(2-hydroxy-5-isopropyl-2,4,6-cycloheptatrien-1-one ...)
Affinity DataIC50:  1.15E+3nMAssay Description:Inhibition of human tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50330795(2-hydroxy-5-isopropyl-2,4,6-cycloheptatrien-1-one ...)
Affinity DataIC50:  1.15E+3nMAssay Description:Inhibition of human tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50559093(CHEMBL4763438)
Affinity DataIC50:  1.40E+3nMAssay Description:Inhibition of human tyrosinase using L- DOPA as substrate by MBTH based assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50205807(CHEMBL3978212)
Affinity DataIC50:  1.50E+3nMAssay Description:Inhibition of tyrosinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50120802(CHEMBL3100130)
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 ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50264085((2S,3R,4S,5R)-2-(2-(2,4-dihydroxyphenethyl)-5-hydr...)
Affinity DataIC50:  1.60E+3nMAssay Description:Inhibition of TyrosinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50219502(4-hydroxyphenyl beta-D-glucopyranoside | Arbutin |...)
Affinity DataIC50: >1.60E+3nMAssay Description:Inhibition of tyrosinase (unknown origin) assessed as reduction in melanin formationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50193667(2,4,3',5'-tetrahydroxybibenzyl | CHEMBL221291)
Affinity DataIC50:  1.60E+3nMAssay Description:Inhibition of tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50559091(CHEMBL4792744)
Affinity DataIC50:  1.60E+3nMAssay Description:Inhibition of human tyrosinase using L- DOPA as substrate by MBTH based assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM23926((E)-resveratrol | 5-[(E)-2-(4-hydroxyphenyl)etheny...)
Affinity DataIC50:  1.70E+3nMAssay Description:Inhibition of human tyrosinase expressed in HEK293 cells using L-tyrosine and DOPA as substrate by absorbance methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50120803(CHEMBL3100134)
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 ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50218211(1'-(4-Methyl-benzyl)-[1,4']bipiperidinyl | CHEMBL3...)
Affinity DataIC50:  1.72E+3nMpH: 6.8 T: 2°CAssay Description:Tyrosinase inhibition assays were performed in a 96-well microplate format using SpectraMax 340 (Molecular Devices, CA, USA) microplate reader accord...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50120804(CHEMBL3618459)
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 ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50240041(1-phenyl-2-thiourea | 1-phenylthiourea | CHEMBL263...)
Affinity DataIC50:  1.80E+3nMAssay Description:Inhibition of tyrosinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50549267(CHEMBL4760852)
Affinity DataIC50:  1.90E+3nMAssay Description:Inhibition of Tyrosinase (unknown origin) using tyrosine as substrate incubated for 20 mins followed by substrate addition and measured every 10 mins...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50174577(CHEMBL3810334)
Affinity DataIC50:  1.95E+3nMAssay Description:Inhibition of tyrosinase (unknown origin) assessed as reduction in monophenolase activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50174577(CHEMBL3810334)
Affinity DataIC50:  1.95E+3nMAssay Description:Inhibition of tyrosinase (unknown origin) assessed as reduction in monophenolase activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosinase(Homo sapiens (Human))
Hiroshima University

Curated by ChEMBL
LigandPNGBDBM50120800(CHEMBL3618460)
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 ArticlePubMed
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