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Found 57 with Last Name = 'ha' and Initial = 'do t'
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Korea Research Institute Of Bioscience And Biotechnology

Curated by ChEMBL
LigandPNGBDBM50303005(CHEMBL570475 | kuwanon J)
Affinity DataIC50:  2.70E+3nMAssay Description:Inhibition of human recombinant PTP1BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Korea Research Institute Of Bioscience And Biotechnology

Curated by ChEMBL
LigandPNGBDBM50303004(CHEMBL562810 | mulberrofuran W)
Affinity DataIC50:  2.70E+3nMAssay Description:Inhibition of human recombinant PTP1BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Korea Research Institute Of Bioscience And Biotechnology

Curated by ChEMBL
LigandPNGBDBM50148911((3beta)-3-hydroxyurs-12-en-28-oic acid | 3beta-hyd...)
Affinity DataIC50:  3.80E+3nMAssay Description:Inhibition of human recombinant PTP1BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute Of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50140241(Allopurinol | Aloral | Aluline 100 | Aluline 300 |...)
Affinity DataIC50:  3.89E+3nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Korea Research Institute Of Bioscience And Biotechnology

Curated by ChEMBL
LigandPNGBDBM50303006(CHEMBL517247 | mulberrofuran D)
Affinity DataIC50:  4.30E+3nMAssay Description:Inhibition of human recombinant PTP1BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Korea Research Institute Of Bioscience And Biotechnology

Curated by ChEMBL
LigandPNGBDBM50104694((R)-4-hydroxy-5-(hydroxymethyl)-3-palmitoylfuran-2...)
Affinity DataIC50:  4.70E+3nMAssay Description:Inhibition of human recombinant PTP1BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Korea Research Institute Of Bioscience And Biotechnology

Curated by ChEMBL
LigandPNGBDBM50303001(CHEMBL570526 | kuwanon R)
Affinity DataIC50:  8.20E+3nMAssay Description:Inhibition of human recombinant PTP1BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Korea Research Institute Of Bioscience And Biotechnology

Curated by ChEMBL
LigandPNGBDBM50303002(CHEMBL564896 | albafuran A)
Affinity DataIC50:  9.20E+3nMAssay Description:Inhibition of human recombinant PTP1BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50310722(CHEMBL575924 | palbinone)
Affinity DataIC50:  1.14E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Korea Research Institute Of Bioscience And Biotechnology

Curated by ChEMBL
LigandPNGBDBM50303003(CHEMBL570609 | kuwanon V)
Affinity DataIC50:  1.38E+4nMAssay Description:Inhibition of human recombinant PTP1BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50310723(30-norhederagenin | CHEMBL1081326)
Affinity DataIC50:  2.88E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50022418((1-Carboxymethyl-cyclopentyl)-acetic acid(TMG) | 3...)
Affinity DataIC50:  3.18E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50310708(4-O-butylpaeoniflorin | CHEMBL1078184)
Affinity DataIC50:  3.62E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50378695(GALLOYLPAEONIFLORIN)
Affinity DataIC50:  4.46E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50310719(CHEMBL1079881 | paeonolide)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50310718(CHEMBL1079227 | paeonol)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50310717(6-methoxypaeoniflorigenone | CHEMBL1081885)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50378697(PAEONIFLORIGENONE)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50310715(CHEMBL1079226 | beta-benzoyloxypaeoniflorin)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50310714(CHEMBL1079225 | alpha-benzoyloxypaeoniflorin)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50310713(CHEMBL1079224 | nudanpinoside H)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50378696(OXYPAEONIFLORIN)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50378694(BENZOYLPAEONIFLORIN)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50378693(PAEONIFLORIN)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50310707(5-hydroxy-3S-hydroxymethyl-6-methyl-2,3-dihydroben...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50310721(CHEMBL1080061 | apiopaeonoside)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50310720(CHEMBL1079882 | paeonoside)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Rattus norvegicus)
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50310706(8-O-benzoylpaeonidanin | CHEMBL1079034)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Sprague-Dawley rat lens alodse reductase by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute Of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50203065(3-phenylacrylaldehyde | 3-phenylprop-2-enal | CHEM...)
Affinity DataIC50:  5.90E+4nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute Of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50485313(Cinnacasolide C)
Affinity DataIC50: >8.52E+4nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute Of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50240642((E)-3-(2-Methoxy-phenyl)-propenal | 2-methoxy cinn...)
Affinity DataIC50:  8.63E+4nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute Of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM7568((2E)-3-(2-hydroxyphenyl)prop-2-enal | Cinnamaldehy...)
Affinity DataIC50:  1.01E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute Of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50485314(Cinnacasolide A)
Affinity DataIC50: >1.12E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute Of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50485315(Cinnacasolide B)
Affinity DataIC50: >1.12E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute Of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50310452(CHEMBL1083511 | rosavin)
Affinity DataIC50: >1.16E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50031467(5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE | 5-Hyd...)
Affinity DataIC50:  1.40E+5nMAssay Description:Inhibition of mushroom tyrosinase after 10 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute Of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50310450(CHEMBL1087939 | methyl dihydromelilotoside)
Affinity DataIC50: >1.46E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute Of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50310449(CHEMBL1087938 | dihydromelilotoside)
Affinity DataIC50: >1.52E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute Of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM16430((2E)-3-phenylprop-2-enoic acid | CHEMBL27246 | Cin...)
Affinity DataIC50:  1.75E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute Of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50146462((2E)-3-(2-hydroxyphenyl)-2-propenoic acid | (2E)-3...)
Affinity DataIC50:  1.94E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute Of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50211193(3-(4-hydroxy-3-methoxyphenyl)prop-2-enal | CHEMBL2...)
Affinity DataIC50:  2.02E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50211193(3-(4-hydroxy-3-methoxyphenyl)prop-2-enal | CHEMBL2...)
Affinity DataIC50:  2.40E+5nMAssay Description:Inhibition of mushroom tyrosinase after 10 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50310445(CHEMBL1077145 | cassiferaldehyde)
Affinity DataIC50:  2.60E+5nMAssay Description:Inhibition of mushroom tyrosinase after 10 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute Of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50310446((E)-3-Phenyl-prop-2-en-1-ol | 3-phenylprop-2-en-1-...)
Affinity DataIC50: >3.72E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM16430((2E)-3-phenylprop-2-enoic acid | CHEMBL27246 | Cin...)
Affinity DataIC50:  4.10E+5nMAssay Description:Inhibition of mushroom tyrosinase after 10 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50240642((E)-3-(2-Methoxy-phenyl)-propenal | 2-methoxy cinn...)
Affinity DataIC50:  4.20E+5nMAssay Description:Inhibition of mushroom tyrosinase after 10 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM7568((2E)-3-(2-hydroxyphenyl)prop-2-enal | Cinnamaldehy...)
Affinity DataIC50:  4.70E+5nMAssay Description:Inhibition of mushroom tyrosinase after 10 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50203065(3-phenylacrylaldehyde | 3-phenylprop-2-enal | CHEM...)
Affinity DataIC50:  5.20E+5nMAssay Description:Inhibition of mushroom tyrosinase after 10 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50310449(CHEMBL1087938 | dihydromelilotoside)
Affinity DataIC50:  5.70E+5nMAssay Description:Inhibition of mushroom tyrosinase after 10 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50310450(CHEMBL1087939 | methyl dihydromelilotoside)
Affinity DataIC50:  6.30E+5nMAssay Description:Inhibition of mushroom tyrosinase after 10 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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