Compile Data Set for Download or QSAR
Found 58 Enz. Inhib. hit(s) with all data for entry = 50044834
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(CHEMBL3360905)copy SMILEScopy InChI
Affinity DataKi:  2.87E+3nMAssay Description:Competitive inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) as...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50343530(5,7-dichloro-4-((3-(4-methoxyphenylthio)benzyl)(me...)copy SMILEScopy InChI
Affinity DataKi:  5.53E+3nMAssay Description:Competitive inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) as...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031908(CHEMBL3360906)copy SMILEScopy InChI
Affinity DataKi:  9.97E+3nMAssay Description:Competitive inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) as...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031910(CHEMBL3360908)copy SMILEScopy InChI
Affinity DataKi:  1.03E+4nMAssay Description:Competitive inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) as...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031905(CHEMBL3360904)copy SMILEScopy InChI
Affinity DataKi:  1.49E+4nMAssay Description:Competitive inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) as...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031907(CHEMBL2337245)copy SMILEScopy InChI
Affinity DataKi:  1.79E+4nMAssay Description:Competitive inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) as...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031909(CHEMBL3360907)copy SMILEScopy InChI
Affinity DataKi:  1.92E+4nMAssay Description:Competitive inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) as...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031904(CHEMBL3360903)copy SMILEScopy InChI
Affinity DataKi:  2.62E+4nMAssay Description:Competitive inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) as...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031911(CHEMBL1299903)copy SMILEScopy InChI
Affinity DataKi:  4.10E+4nMAssay Description:Covalent irreversible inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL2...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(CHEMBL3360905)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of PTP1B (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(CHEMBL3360905)copy SMILEScopy InChI
Affinity DataIC50: 6.10E+3nMAssay Description:Inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) assessed as re...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031916(CHEMBL3360912)copy SMILEScopy InChI
Affinity DataIC50: 7.10E+3nMAssay Description:Inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) assessed as re...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(CHEMBL3360905)copy SMILEScopy InChI
Affinity DataIC50: 7.60E+3nMAssay Description:Inhibition of VHR (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 9(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(CHEMBL3360905)copy SMILEScopy InChI
Affinity DataIC50: 1.07E+4nMAssay Description:Inhibition of MEG2 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 5(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(CHEMBL3360905)copy SMILEScopy InChI
Affinity DataIC50: 1.66E+4nMAssay Description:Inhibition of STEP (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031908(CHEMBL3360906)copy SMILEScopy InChI
Affinity DataIC50: 1.85E+4nMAssay Description:Inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) assessed as re...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetProtein phosphatase 1A(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50343530(5,7-dichloro-4-((3-(4-methoxyphenylthio)benzyl)(me...)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+4nMAssay Description:Inhibition of PPM1A (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 18(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(CHEMBL3360905)copy SMILEScopy InChI
Affinity DataIC50: 2.64E+4nMAssay Description:Inhibition of PTPN18 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031920(CHEMBL3360916)copy SMILEScopy InChI
Affinity DataIC50: 2.76E+4nMAssay Description:Inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) assessed as re...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 18(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031910(CHEMBL3360908)copy SMILEScopy InChI
Affinity DataIC50: 2.97E+4nMAssay Description:Inhibition of PTPN18 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetProtein phosphatase 1A(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031908(CHEMBL3360906)copy SMILEScopy InChI
Affinity DataIC50: 3.18E+4nMAssay Description:Inhibition of PPM1A (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031913(CHEMBL3360910)copy SMILEScopy InChI
Affinity DataIC50: 3.65E+4nMAssay Description:Inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) assessed as re...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 9(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031908(CHEMBL3360906)copy SMILEScopy InChI
Affinity DataIC50: 3.75E+4nMAssay Description:Inhibition of MEG2 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50343530(5,7-dichloro-4-((3-(4-methoxyphenylthio)benzyl)(me...)copy SMILEScopy InChI
Affinity DataIC50: 3.88E+4nMAssay Description:Inhibition of PTP1B (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031917(CHEMBL3360913)copy SMILEScopy InChI
Affinity DataIC50: 3.92E+4nMAssay Description:Inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) assessed as re...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031919(CHEMBL3360915)copy SMILEScopy InChI
Affinity DataIC50: 4.14E+4nMAssay Description:Inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) assessed as re...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031918(CHEMBL3360914)copy SMILEScopy InChI
Affinity DataIC50: 4.17E+4nMAssay Description:Inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) assessed as re...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031912(CHEMBL3360909)copy SMILEScopy InChI
Affinity DataIC50: 4.20E+4nMAssay Description:Inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) assessed as re...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetProtein phosphatase 1A(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031910(CHEMBL3360908)copy SMILEScopy InChI
Affinity DataIC50: 4.25E+4nMAssay Description:Inhibition of PPM1A (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031946(CHEMBL3360917)copy SMILEScopy InChI
Affinity DataIC50: 4.87E+4nMAssay Description:Inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) assessed as re...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031908(CHEMBL3360906)copy SMILEScopy InChI
Affinity DataIC50: 5.01E+4nMAssay Description:Inhibition of VHR (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50343530(5,7-dichloro-4-((3-(4-methoxyphenylthio)benzyl)(me...)copy SMILEScopy InChI
Affinity DataIC50: 5.07E+4nMAssay Description:Inhibition of VHR (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 5(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50343530(5,7-dichloro-4-((3-(4-methoxyphenylthio)benzyl)(me...)copy SMILEScopy InChI
Affinity DataIC50: 6.06E+4nMAssay Description:Inhibition of STEP (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031910(CHEMBL3360908)copy SMILEScopy InChI
Affinity DataIC50: 6.38E+4nMAssay Description:Inhibition of PTP1B (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 9(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50343530(5,7-dichloro-4-((3-(4-methoxyphenylthio)benzyl)(me...)copy SMILEScopy InChI
Affinity DataIC50: 6.61E+4nMAssay Description:Inhibition of MEG2 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetProtein phosphatase 1A(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(CHEMBL3360905)copy SMILEScopy InChI
Affinity DataIC50: 6.78E+4nMAssay Description:Inhibition of PPM1A (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetProtein phosphatase 1G(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50343530(5,7-dichloro-4-((3-(4-methoxyphenylthio)benzyl)(me...)copy SMILEScopy InChI
Affinity DataIC50: 7.48E+4nMAssay Description:Inhibition of PPM1G (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 9(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031910(CHEMBL3360908)copy SMILEScopy InChI
Affinity DataIC50: 7.85E+4nMAssay Description:Inhibition of MEG2 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031914(CHEMBL3196685)copy SMILEScopy InChI
Affinity DataIC50: 7.95E+4nMAssay Description:Inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) assessed as re...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 5(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031908(CHEMBL3360906)copy SMILEScopy InChI
Affinity DataIC50: 9.60E+4nMAssay Description:Inhibition of STEP (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031915(CHEMBL3360911)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of N-terminal His-tagged Lyp (unknown origin) catalytic domain (1 to 294 residues) expressed in Escherichia coli BL21 (DE3) assessed as re...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031908(CHEMBL3360906)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of PTP1B (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 5(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031910(CHEMBL3360908)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of STEP (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 18(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031908(CHEMBL3360906)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of PTPN18 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031910(CHEMBL3360908)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of VHR (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetProtein phosphatase Slingshot homolog 2(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50343530(5,7-dichloro-4-((3-(4-methoxyphenylthio)benzyl)(me...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of SSH2 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetProtein phosphatase Slingshot homolog 2(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(CHEMBL3360905)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of SSH2 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetProtein phosphatase Slingshot homolog 2(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031908(CHEMBL3360906)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of SSH2 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetProtein phosphatase Slingshot homolog 2(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031910(CHEMBL3360908)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of SSH2 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
TargetTyrosine-protein phosphatase non-receptor type 18(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50343530(5,7-dichloro-4-((3-(4-methoxyphenylthio)benzyl)(me...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of PTPN18 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6TVJPubMed
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