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Found 16 with Last Name = 'park' and Initial = 'th'
TargetReceptor-type tyrosine-protein phosphatase S(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50456401(IRIGENOL)
Affinity DataIC50:  500nMAssay Description:Inhibition of recombinant human PTP-sigma (residues 1367 to 1948) using para-nitrophenylphosphate as substrate for 60 mins by fluorescence analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein phosphatase S(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM23411(5,6,7-trihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-...)
Affinity DataIC50:  600nMAssay Description:Inhibition of recombinant human PTP-sigma (residues 1367 to 1948) using para-nitrophenylphosphate as substrate for 60 mins by fluorescence analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein phosphatase S(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50499947(CHEMBL3739950)
Affinity DataIC50:  800nMAssay Description:Inhibition of recombinant human PTP-sigma (residues 1367 to 1948) using para-nitrophenylphosphate as substrate for 60 mins by fluorescence analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein phosphatase S(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50499946(CHEMBL3740878)
Affinity DataIC50:  900nMAssay Description:Inhibition of recombinant human PTP-sigma (residues 1367 to 1948) using para-nitrophenylphosphate as substrate for 60 mins by fluorescence analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein phosphatase S(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM26661(7,3,4,5-tetrahydroxyflavone | 7-hydroxy-2-(3,4,5-t...)
Affinity DataIC50:  3.00E+3nMAssay Description:Inhibition of recombinant human PTP-sigma (residues 1367 to 1948) using para-nitrophenylphosphate as substrate for 60 mins by fluorescence analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein phosphatase S(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM26658(2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-1-benzopy...)
Affinity DataIC50:  4.30E+3nMAssay Description:Inhibition of recombinant human PTP-sigma (residues 1367 to 1948) using para-nitrophenylphosphate as substrate for 60 mins by fluorescence analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein phosphatase S(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50499945(CHEMBL3740356)
Affinity DataIC50:  5.40E+3nMAssay Description:Inhibition of recombinant human PTP-sigma (residues 1367 to 1948) using para-nitrophenylphosphate as substrate for 60 mins by fluorescence analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein phosphatase S(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50499944(CHEMBL3739990)
Affinity DataIC50:  6.60E+3nMAssay Description:Inhibition of recombinant human PTP-sigma (residues 1367 to 1948) using para-nitrophenylphosphate as substrate for 60 mins by fluorescence analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein phosphatase S(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50391109(CHEMBL179166 | Sodium orthovanadate (SOV) | Vanada...)
Affinity DataIC50:  8.30E+3nMAssay Description:Inhibition of recombinant human PTP-sigma (residues 1367 to 1948) using para-nitrophenylphosphate as substrate for 60 mins by fluorescence analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein phosphatase S(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50009001(5,6,7-Trihydroxyflavone | 5,6,7-trihydroxy-2-pheny...)
Affinity DataIC50:  1.03E+4nMAssay Description:Inhibition of recombinant human PTP-sigma (residues 1367 to 1948) using para-nitrophenylphosphate as substrate for 60 mins by fluorescence analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein phosphatase S(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50499948(CHEMBL3741920)
Affinity DataIC50:  1.04E+4nMAssay Description:Inhibition of recombinant human PTP-sigma (residues 1367 to 1948) using para-nitrophenylphosphate as substrate for 60 mins by fluorescence analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein phosphatase S(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM26656(5,7,3,4,5-pentahydroxyflavone | 5,7-dihydroxy-2-(3...)
Affinity DataIC50:  1.75E+4nMAssay Description:Inhibition of recombinant human PTP-sigma (residues 1367 to 1948) using para-nitrophenylphosphate as substrate for 60 mins by fluorescence analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamine-dependent NAD(+) synthetase(Homo sapiens (Human))
National Institutes Of Health

LigandPNGBDBM92599(CHEMBL263057 | NAD Synthetase Inhibitor, 4)
Affinity DataIC50:  2.18E+4nMpH: 8.5 T: 2°CAssay Description:Inhibition assay using NAD synthetase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamine-dependent NAD(+) synthetase(Homo sapiens (Human))
National Institutes Of Health

LigandPNGBDBM92597(CHEMBL324501 | NAD Synthetase Inhibitor, 2)
Affinity DataIC50:  2.48E+4nMpH: 8.5 T: 2°CAssay Description:Inhibition assay using NAD synthetase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamine-dependent NAD(+) synthetase(Homo sapiens (Human))
National Institutes Of Health

LigandPNGBDBM92600(CHEMBL419944 | NAD Synthetase Inhibitor, 5)
Affinity DataIC50:  5.78E+4nMpH: 8.5 T: 2°CAssay Description:Inhibition assay using NAD synthetase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamine-dependent NAD(+) synthetase(Homo sapiens (Human))
National Institutes Of Health

LigandPNGBDBM92598(NAD Synthetase Inhibitor, 3)
Affinity DataIC50:  6.33E+4nMpH: 8.5 T: 2°CAssay Description:Inhibition assay using NAD synthetase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed