Compile Data Set for Download or QSAR
Report error Found 120 Enz. Inhib. hit(s) with all data for entry = 50018758
TargetPeroxisome proliferator-activated receptor gamma(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612113(CHEMBL2435489)
Affinity DataEC50: >4.74E+4nMAssay Description:Agonist activity at Gal4-PPARgamma (unknown origin) transfected in HCT-116 cells incubated for 24 hrs by luciferase reporter assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAldo-keto reductase family 1 member B1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM16315(CP-744809 | CHEMBL240725 | 6-[(5-chloro-3-methyl-1...)
Affinity DataIC50: 1nMAssay Description:Inhibition of human recombinant Aldose reductaseMore data for this Ligand-Target Pair
In DepthDetails
PubMedPDB3D3D Structure (crystal)
TargetAldo-keto reductase family 1 member B1(Rat)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50122956([2,4-Bis-(4-methoxy-benzoyl)-pyrrol-1-yl]-acetic a...)
Affinity DataIC50: 2.40nMAssay Description:Inhibition of ALR in Fischer-344 rat lens using D,L-glyceraldehyde as substrate in presence of NADPH measured after 3 mins by spectrophotometric assa...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612104(CHEMBL5290902)
Affinity DataIC50: 5nMAssay Description:Inhibition of human PTP1B (1 to 298 residues) expressed in Escherichia coli using FDP as substrate by microplate readerMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612109(CHEMBL5275241)
Affinity DataIC50: 5nMAssay Description:Inhibition of PTP1B (unknown origin) using pNPP as substrateMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50142311([(4-{2-[4-(Difluoro-phosphono-methyl)-benzyl]-3-ox...)
Affinity DataIC50: 6nMAssay Description:Inhibition of human PTP1B (1 to 321 residues) expressed in Escherichia coli using FDP as substrateMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612064(CHEMBL5285288)
Affinity DataIC50: 6nMAssay Description:Inhibition of human PTP1B (1 to 321 residues) expressed in Escherichia coli using FDP as substrateMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50142318({[2-Chloro-4-(3-oxo-2,3-diphenyl-propyl)-phenyl]-d...)
Affinity DataIC50: 6nMAssay Description:Inhibition of human PTP1B (1 to 321 residues) expressed in Escherichia coli using FDP as substrateMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50142317((2-bromo-4-(3-oxo-2,3-diphenylpropyl)phenyl)difluo...)
Affinity DataIC50: 6nMAssay Description:Inhibition of human PTP1B (1 to 321 residues) expressed in Escherichia coli using FDP as substrateMore data for this Ligand-Target Pair
In DepthDetails
PubMedPDB3D3D Structure (crystal)
TargetAldo-keto reductase family 1 member B1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612073(CHEMBL5286261)
Affinity DataIC50: 6nMAssay Description:Inhibition of human recombinant ALR2 expressed in Escherichia coli by Coomassie reagent assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612102(CHEMBL5273366)
Affinity DataIC50: 13nMAssay Description:Inhibition of human PTP1B (1 to 298 residues) expressed in Escherichia coli using FDP as substrate by microplate readerMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612101(CHEMBL5289453)
Affinity DataIC50: 16nMAssay Description:Inhibition of human PTP1B (1 to 298 residues) expressed in Escherichia coli using FDP as substrate by microplate readerMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612103(CHEMBL5268825)
Affinity DataIC50: 23nMAssay Description:Inhibition of human PTP1B (1 to 298 residues) expressed in Escherichia coli using FDP as substrate by microplate readerMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAldo-keto reductase family 1 member B1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM16313(IDD594 | LdT | CHEMBL395347 | {2-[(4-bromo-2-fluor...)
Affinity DataIC50: 30nMAssay Description:Inhibition of human recombinant ALR2 expressed in Escherichia coli by Coomassie reagent assayMore data for this Ligand-Target Pair
In DepthDetails
PubMedPDB3D3D Structure (crystal)
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM13814(({4-[(4E)-2-(1H-1,2,3-benzotriazol-1-yl)-2-[4-(met...)
Affinity DataIC50: 39nMAssay Description:Inhibition of Flag-tagged human PTP1B (1 to 298 residues) expressed in Escherichia coli BL21 using FDP as substrateMore data for this Ligand-Target Pair
In DepthDetails
PubMedPDB3D3D Structure (crystal)
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50142312(2,2-Bis-[4-(difluoro-phosphono-methyl)-benzyl]-mal...)
Affinity DataIC50: 40nMAssay Description:Inhibition of human PTP1B (1 to 321 residues) expressed in Escherichia coli using FDP as substrateMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50142313(2,2-Bis-[4-(difluoro-phosphono-methyl)-benzyl]-mal...)
Affinity DataIC50: 40nMAssay Description:Inhibition of human PTP1B (1 to 321 residues) expressed in Escherichia coli using FDP as substrateMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50142307(2,2-Bis-[4-(difluoro-phosphono-methyl)-benzyl]-mal...)
Affinity DataIC50: 40nMAssay Description:Inhibition of human PTP1B (1 to 321 residues) expressed in Escherichia coli using FDP as substrateMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612063(CHEMBL5271227)
Affinity DataIC50: 40nMAssay Description:Inhibition of human PTP1B (1 to 321 residues) expressed in Escherichia coli using FDP as substrateMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAldo-keto reductase family 1 member B1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612080(CHEMBL5273049)
Affinity DataIC50: 40nMAssay Description:Inhibition of ALR2 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAldo-keto reductase family 1 member B1(Rat)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612070(CHEMBL5286592)
Affinity DataIC50: 45nMAssay Description:Inhibition of ALR in Fischer-344 rat lens using D,L-glyceraldehyde as substrate in presence of NADPH measured after 3 mins by spectrophotometric assa...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAldo-keto reductase family 1 member B1(Rat)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612069(CHEMBL5279574)
Affinity DataIC50: 49nMAssay Description:Inhibition of ALR in Fischer-344 rat lens using D,L-glyceraldehyde as substrate in presence of NADPH measured after 3 mins by spectrophotometric assa...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAldo-keto reductase family 1 member B1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612081(CHEMBL5271166)
Affinity DataIC50: 60nMAssay Description:Inhibition of ALR2 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50543509(CHEMBL4636119)
Affinity DataIC50: 70nMAssay Description:Inhibition of human PTP1B using pNPP as substrate incubated for 30 min by microplate reader assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612089(CHEMBL5281085)
Affinity DataIC50: 72nMAssay Description:Inhibition of PTP1B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50090172((R)-2-[4-(2,3-Dimethyl-1-oxa-9-thia-cyclopenta[b]f...)
Affinity DataIC50: 74nMAssay Description:Inhibition of human recombinant PTP1B (1 to 321 residues) expressed in Escherichia coli using TRDIYETDYYRK as peptide substrate incubated for 30 mins...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM15819(1:1 mixture of diastereomers | CHEMBL55243 | 2-[(4...)
Affinity DataIC50: 77nMAssay Description:Inhibition of PTP1B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612105(CHEMBL5268430)
Affinity DataIC50: 80nMAssay Description:Inhibition of human PTP1B (1 to 411 residues) expressed in Escherichia coli BL21 (DE3) using GNGDpYMPMSPKS as phosphopeptide substrate incubated for ...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612106(CHEMBL5267772)
Affinity DataIC50: 80nMAssay Description:Inhibition of human PTP1B (1 to 411 residues) expressed in Escherichia coli BL21 (DE3) using GNGDpYMPMSPKS as phosphopeptide substrate incubated for ...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612107(CHEMBL5265859)
Affinity DataIC50: 80nMAssay Description:Inhibition of human PTP1B (1 to 411 residues) expressed in Escherichia coli BL21 (DE3) using GNGDpYMPMSPKS as phosphopeptide substrate incubated for ...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612108(CHEMBL1208413)
Affinity DataIC50: 80nMAssay Description:Inhibition of human PTP1B (1 to 411 residues) expressed in Escherichia coli BL21 (DE3) using GNGDpYMPMSPKS as phosphopeptide substrate incubated for ...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50079855((R)-2-[2,6-Dibromo-4-(6-bromo-benzo[b]naphtho[2,3-...)
Affinity DataIC50: 83nMAssay Description:Inhibition of human recombinant PTP1B (1 to 321 residues) expressed in Escherichia coli using TRDIYETDYYRK as peptide substrate incubated for 30 mins...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM13814(({4-[(4E)-2-(1H-1,2,3-benzotriazol-1-yl)-2-[4-(met...)
Affinity DataIC50: 87nMAssay Description:Inhibition of Flag-tagged human TCPTP (1 to 296 residues) expressed in Escherichia coli BL21 using FDP as substrateMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612091(CHEMBL5282419)
Affinity DataIC50: 90nMAssay Description:Inhibition of PTP1B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612096(CHEMBL5272918)
Affinity DataIC50: 106nMAssay Description:Inhibition of PTP1B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetPlatelet-derived growth factor receptor alpha/beta(Mouse)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612116(CHEMBL5272219)
Affinity DataIC50: 110nMAssay Description:Inhibition of yeast alpha-glucosidase using PNP-G as substrate preincubated for 10 mins followed by substrate addition by spectrophotometer microplat...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50085944([2-(3-{3-[5-Methyl-2-(4-trifluoromethyl-phenyl)-ox...)
Affinity DataIC50: 120nMAssay Description:Inhibition of PTP1B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612098(CHEMBL5269933)
Affinity DataIC50: 140nMAssay Description:Inhibition of PTP1B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50085962((Z)[2-(3-{3-[5-Methyl-2-(4-trifluoromethyl-phenyl)...)
Affinity DataIC50: 160nMAssay Description:Inhibition of PTP1B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612061(CHEMBL5278919)
Affinity DataIC50: 163nMAssay Description:Inhibition of Flag-tagged human PTP1B (1 to 298 residues) expressed in Escherichia coli BL21 using FDP as substrateMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612097(CHEMBL5272799)
Affinity DataIC50: 180nMAssay Description:Inhibition of PTP1B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAldo-keto reductase family 1 member B1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM104024(MK315)
Affinity DataIC50: 190nMAssay Description:Inhibition of Aldose reductase (unknown origin) using D,L-glyceraldehyde as substrate preincubated for 5 mins in presence of NADPH followed by substr...More data for this Ligand-Target Pair
In DepthDetails
PubMedPDB3D3D Structure (crystal)
TargetAldo-keto reductase family 1 member B1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50554698(CHEMBL4782682)
Affinity DataIC50: 190nMAssay Description:Inhibition of ALR2 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612087(CHEMBL5287985)
Affinity DataIC50: 200nMAssay Description:Inhibition of PTP1B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612093(CHEMBL5272037)
Affinity DataIC50: 200nMAssay Description:Inhibition of PTP1B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50568470(CHEMBL4876185)
Affinity DataIC50: 280nMAssay Description:Inhibition of human PTP1B using pNPP as substrate incubated for 30 minMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50090171((R)-2-[4-(2,3-Dimethyl-1-oxa-9-thia-cyclopenta[b]f...)
Affinity DataIC50: 284nMAssay Description:Inhibition of human recombinant PTP1B (1 to 321 residues) expressed in Escherichia coli using TRDIYETDYYRK as peptide substrate incubated for 30 mins...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50085948(2-(3-{3-[5-Phenyl-2-(4-trifluoromethyl-phenyl)-oxa...)
Affinity DataIC50: 300nMAssay Description:Inhibition of PTP1B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50409191(CHEMBL365490)
Affinity DataIC50: 322nMAssay Description:Inhibition of human recombinant PTP1B (1 to 321 residues) expressed in Escherichia coli using TRDIYETDYYRK as peptide substrate incubated for 30 mins...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAldo-keto reductase family 1 member B1(Human)
Aristotle University of Thessaloniki

Curated by ChEMBL
LigandPNGBDBM50612082(CHEMBL5290848)
Affinity DataIC50: 350nMAssay Description:Inhibition of Aldose reductase in human muscle tissue using D,L-glyceraldehyde as substrate in presence of NADPH by spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
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