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Found 23 of ph data with Target = 'Dual specificity protein phosphatase 3'
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM199180(US9217012, 10)
Affinity DataKi: >1.00E+3nM ΔG°: >-34.2kJ/molepH: 7.0 T: 2°CAssay Description:PTP activity was assayed using p-nitrophenyl phosphate (pNPP) as a substrate in DMG buffer (50 mM DMG, pH 7.0, 1 mM EDTA, 150 mM NaCl, 2 mM DTT, 0.1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM26104(5-{2-cyclohexyl-4-[4-fluoro-3-(trifluoromethyl)phe...)
Affinity DataKi: >5.00E+4nM ΔG°: >-24.3kJ/molepH: 7.4 T: 2°CAssay Description:The reaction was started by addition of pNPP substrate, and reaction progress was monitored at 405 nm. The initial rate data collected was used for d...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM84499(2-(5-{1-[(2Z)-2H-pyrrol-2-ylidene]ethyl}furan-2-yl...)
Affinity DataIC50:  4.90E+3nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM50087856(CHEMBL3426913)
Affinity DataIC50:  6.00E+3nMpH: 7.0Assay Description:Inhibition of VHR (unknown origin) using pNPP as substrate at pH 7 at 25 degC by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM84496(Roseophilin, 2)
Affinity DataIC50:  6.00E+3nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM84511(Acyclic analogue, 16)
Affinity DataIC50:  8.00E+3nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM84498(3-chloro-2-(5-{1-[(2Z)-2H-pyrrol-2-ylidene]ethyl}f...)
Affinity DataIC50:  9.00E+3nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM84506(Acyclic analogue, 12)
Affinity DataIC50:  9.00E+3nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM231167(US9340574, 7)
Affinity DataIC50: >1.00E+4nMpH: 7.0Assay Description:PTP activity was assayed using p-nitrophenyl phosphate (pNPP) as a substrate in 3,3-dimethylglutarate buffer (50 mM 3,3-dimethylglutarate, pH 7.0, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM84507(Acyclic analogue, 13)
Affinity DataIC50:  1.10E+4nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM84497(Roseophilin analogue, 3)
Affinity DataIC50:  1.50E+4nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM84512(Acyclic analogue, 18)
Affinity DataIC50:  2.10E+4nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM84500(Nonylprodigiosin, 6)
Affinity DataIC50:  2.10E+4nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM84508(Acyclic analogue, 14)
Affinity DataIC50:  2.10E+4nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM84501(Cyclic analogue, 7)
Affinity DataIC50:  2.80E+4nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM84503(Cyclic analogue, 9)
Affinity DataIC50:  3.00E+4nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM84495(CHEMBL1945189 | Roseophilin, 1)
Affinity DataIC50:  3.20E+4nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM84509(Acyclic analogue, 15)
Affinity DataIC50:  3.90E+4nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM84502(Cyclic analogue, 8)
Affinity DataIC50:  4.10E+4nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM84510(Acyclic analogue, 17)
Affinity DataIC50: >5.00E+4nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM84505(Acyclic analogue, 11)
Affinity DataIC50: >5.00E+4nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM84504(Acyclic analogue, 10)
Affinity DataIC50: >5.00E+4nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Indiana University Research And Technology

US Patent
LigandPNGBDBM50308158(3-(1-(3-(Biphenyl-4-ylamino)-3-oxopropyl)-1H-1,2,3...)
Affinity DataIC50: >5.00E+4nMpH: 7.0Assay Description:Inhibition of VHR expressed in Escherichia coli assessed as inhibition of p-nitrophenyl phosphate hydrolysis at pH 7 by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed