Compile Data Set for Download or QSAR
Report error Found 39 of affinity data for UniProtKB/TrEMBL: P20417
LigandChemical structure of BindingDB Monomer ID 13614BDBM13614(2-(carboxymethoxy)-5-[(2S)-2-(pentylcarbamoyl)-2-[...)
Affinity DataKi:  120nM ΔG°:  -39.1kJ/molepH: 7.2 T: 2°CAssay Description:Hydrolysis of substrate p-nitrophenyl phosphate was monitored on a 96-well microplate reader. Concentrations of PTP1B inhibitors that resulted in 50%...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/6/2007
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 13611BDBM13611(2-(carboxymethoxy)-5-[(2S)-2-[(2S)-2-(3-formamidop...)
Affinity DataKi:  250nM ΔG°:  -37.3kJ/molepH: 7.2 T: 2°CAssay Description:Hydrolysis of substrate p-nitrophenyl phosphate was monitored on a 96-well microplate reader. Concentrations of PTP1B inhibitors that resulted in 50%...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/6/2007
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085948BDBM50085948(2-(3-{3-[5-Phenyl-2-(4-trifluoromethyl-phenyl)-oxa...)
Affinity DataIC50: 300nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085938BDBM50085938(2-{3-[3-(3,5-Dichloro-benzyloxy)-phenyl]-hept-2-en...)
Affinity DataIC50: 800nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 13609BDBM13609(2-{4-[(2S)-2-[(2S)-2-(3-formamidopropanoic acid)-3...)
Affinity DataKi:  1.20E+3nM ΔG°:  -33.5kJ/molepH: 7.2 T: 2°CAssay Description:Hydrolysis of substrate p-nitrophenyl phosphate was monitored on a 96-well microplate reader. Concentrations of PTP1B inhibitors that resulted in 50%...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/6/2007
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085965BDBM50085965(2-{3-[3-(2-Butyl-benzofuran-3-ylmethyl)-phenyl]-bu...)
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085956BDBM50085956(2-[3-(4-{2-[5-Methyl-2-(4-trifluoromethyl-phenyl)-...)
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085942BDBM50085942(2-{3-[3-(3,5-Dichloro-phenoxy)-phenyl]-hept-2-enyl...)
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085938BDBM50085938(2-{3-[3-(3,5-Dichloro-benzyloxy)-phenyl]-hept-2-en...)
Affinity DataIC50: 1.80E+3nMAssay Description:Inhibition of PTPase activity using recombinant Protein-tyrosine phosphatase 1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085941BDBM50085941(2-[3-(3-Phenoxy-phenyl)-hept-2-enyl]-[1,2,4]oxadia...)
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085961BDBM50085961(2-{3-[3-(2-Butyl-benzofuran-3-ylmethoxy)-phenyl]-b...)
Affinity DataIC50: 2.70E+3nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 13610BDBM13610(2-(carboxymethoxy)-5-[(2S)-2-(3-formamidopropanoic...)
Affinity DataKi:  2.80E+3nM ΔG°:  -31.4kJ/molepH: 7.2 T: 2°CAssay Description:Hydrolysis of substrate p-nitrophenyl phosphate was monitored on a 96-well microplate reader. Concentrations of PTP1B inhibitors that resulted in 50%...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/6/2007
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085967BDBM50085967(2-{3-[3-(5-Phenyl-[1,2,4]oxadiazol-3-ylmethoxy)-ph...)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 13613BDBM13613(2-{4-[(2S)-2-({[(1S)-1-carboxy-2-phenylethyl]carba...)
Affinity DataKi:  3.40E+3nM ΔG°:  -30.9kJ/molepH: 7.2 T: 2°CAssay Description:Hydrolysis of substrate p-nitrophenyl phosphate was monitored on a 96-well microplate reader. Concentrations of PTP1B inhibitors that resulted in 50%...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/6/2007
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085958BDBM50085958(2-(3-{3-[5-Methyl-2-(4-trifluoromethyl-phenyl)-oxa...)
Affinity DataIC50: 3.80E+3nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085960BDBM50085960(2-{(E)-3-[3-(3,5-Bis-trifluoromethyl-benzyloxy)-ph...)
Affinity DataIC50: 4.10E+3nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 13606BDBM13606(CHEMBL175257 | N-acetyl-Asp-Tyr(SO3H)-Nle-NH2 | (3...)
Affinity DataKi:  5.00E+3nM ΔG°:  -30.0kJ/molepH: 7.2 T: 2°CAssay Description:Hydrolysis of substrate p-nitrophenyl phosphate was monitored on a 96-well microplate reader. Concentrations of PTP1B inhibitors that resulted in 50%...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/6/2007
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 13606BDBM13606(CHEMBL175257 | N-acetyl-Asp-Tyr(SO3H)-Nle-NH2 | (3...)
Affinity DataKi:  5.00E+3nMAssay Description:Inhibition of rat recombinant PTP1B (1 to 321 residues) expressed in Escherichia coli BL21 assessed as inhibition constant using pNPP as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/21/2024
Entry Details
PubMed
LigandChemical structure of BindingDB Monomer ID 50440661BDBM50440661(CHEMBL2430649)
Affinity DataIC50: 8.61E+3nMAssay Description:Inhibition of PTP1B in rat liver homogenates using p-nitro phenyl phosphate as substrate preincubated for 30 mins followed by substrate addition meas...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article

LigandChemical structure of BindingDB Monomer ID 50085952BDBM50085952(2-{3-[3-(4-Methoxy-phenoxy)-phenyl]-hept-2-enyl}-[...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085963BDBM50085963(2-{3-[3-(3,5-Bis-trifluoromethyl-phenoxymethyl)-ph...)
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 13608BDBM13608(2-{4-[(2S)-2-(3-formamidopropanoic acid)-2-(pentyl...)
Affinity DataKi:  1.20E+4nM ΔG°:  -27.8kJ/molepH: 7.2 T: 2°CAssay Description:Hydrolysis of substrate p-nitrophenyl phosphate was monitored on a 96-well microplate reader. Concentrations of PTP1B inhibitors that resulted in 50%...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/6/2007
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085945BDBM50085945(1-(3-{3-[5-Methyl-2-(4-trifluoromethyl-phenyl)-oxa...)
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085939BDBM50085939(2-[3-(3-p-Tolyloxy-phenyl)-hept-2-enyl]-[1,2,4]oxa...)
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085955BDBM50085955(2-{3-[3-(5-Chloro-naphthalen-2-ylmethoxy)-phenyl]-...)
Affinity DataIC50: 1.60E+4nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085949BDBM50085949(2-(3-{3-[2-(4-Trifluoromethyl-phenyl)-oxazol-4-ylm...)
Affinity DataIC50: 1.90E+4nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50440662BDBM50440662(CHEMBL2430648)
Affinity DataIC50: 2.04E+4nMAssay Description:Inhibition of PTP1B in rat liver homogenates using p-nitro phenyl phosphate as substrate preincubated for 30 mins followed by substrate addition meas...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article

LigandChemical structure of BindingDB Monomer ID 50085942BDBM50085942(2-{3-[3-(3,5-Dichloro-phenoxy)-phenyl]-hept-2-enyl...)
Affinity DataIC50: 2.30E+4nMAssay Description:Inhibition of PTPase activity in rat hepatic membrane at a concentration of 50 uM using pNPP as the substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085959BDBM50085959(2-(3-{3-[2-(5-Methyl-2-phenyl-oxazol-4-yl)-ethoxy]...)
Affinity DataIC50: 2.40E+4nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085950BDBM50085950(2-(4,4-Dimethyl-3-{3-[5-methyl-2-(4-trifluoromethy...)
Affinity DataIC50: 2.40E+4nMAssay Description:Inhibition of PTPase activity in rat hepatic membrane at a concentration of 50 uM using pNPP as the substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085969BDBM50085969(2-(3-{3-[3-(3,5-Bis-trifluoromethyl-phenyl)-prop-2...)
Affinity DataIC50: 2.50E+4nMAssay Description:Concentration required to inhibit PTPase activity, recombinant r-PTP1B as the enzyme at a concentration 2.5 uM. More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085946BDBM50085946(2-(3-(4-Chloro-phenyl)-3-{3-[5-methyl-2-(4-trifluo...)
Affinity DataIC50: 2.70E+4nMAssay Description:Inhibition of PTPase activity in rat hepatic membrane at a concentration of 50 uM using pNPP as the substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085966BDBM50085966(2-(3-(4-Fluoro-phenyl)-3-{3-[5-methyl-2-(4-trifluo...)
Affinity DataIC50: 2.80E+4nMAssay Description:Inhibition of PTPase activity in rat hepatic membrane at a concentration of 50 uM using pNPP as the substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 13607BDBM13607(Compound II | 3-{[(1S)-1-(pentylcarbamoyl)-2-[4-(s...)
Affinity DataKi:  3.00E+4nM ΔG°:  -25.6kJ/molepH: 7.2 T: 2°CAssay Description:Hydrolysis of substrate p-nitrophenyl phosphate was monitored on a 96-well microplate reader. Concentrations of PTP1B inhibitors that resulted in 50%...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/6/2007
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085961BDBM50085961(2-{3-[3-(2-Butyl-benzofuran-3-ylmethoxy)-phenyl]-b...)
Affinity DataIC50: 3.30E+4nMAssay Description:Inhibition of PTPase activity in rat hepatic membrane at a concentration of 50 uM using pNPP as the substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085957BDBM50085957(2-(3-{2-[5-Methyl-2-(4-trifluoromethyl-phenyl)-oxa...)
Affinity DataIC50: 4.30E+4nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085964BDBM50085964(5-(3-{3-[5-Methyl-2-(4-trifluoromethoxy-phenyl)-ox...)
Affinity DataIC50: 4.60E+4nMAssay Description:Inhibition of PTPase activity using recombinant r-PTP1B as the enzyme and IR-triphosphopeptide as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50085940BDBM50085940(2-(2-Methyl-3-{3-[5-methyl-2-(4-trifluoromethyl-ph...)
Affinity DataIC50: 7.10E+4nMAssay Description:Inhibition of PTPase activity in rat hepatic membrane at a concentration of 50 uM using pNPP as the substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 13612BDBM13612(methyl 2-(2-methoxy-2-oxoethoxy)-5-[(2S)-2-[(2S)-2...)
Affinity DataKi: >1.00E+5nM ΔG°: >-22.6kJ/molepH: 7.2 T: 2°CAssay Description:Hydrolysis of substrate p-nitrophenyl phosphate was monitored on a 96-well microplate reader. Concentrations of PTP1B inhibitors that resulted in 50%...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/6/2007
Entry Details Article
PubMed