Compile Data Set for Download or QSAR
Report error Found 58 Enz. Inhib. hit(s) with all data for entry = 50044834
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031906BDBM50031906(CHEMBL3360905)
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of PTP1B (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031906BDBM50031906(CHEMBL3360905)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50343530BDBM50343530(5,7-dichloro-4-((3-(4-methoxyphenylthio)benzyl)(me...)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031906BDBM50031906(CHEMBL3360905)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031906BDBM50031906(CHEMBL3360905)
Affinity DataEC50:  6.49E+3nMAssay Description:Inhibition of Lyp in antiCD3-antibody-stimulated human Jurkat T cells assessed as activation of TCR-mediated and IL-2 promoter driven NFAT/AP1 transc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031916BDBM50031916(CHEMBL3360912)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetDual specificity protein phosphatase 3(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031906BDBM50031906(CHEMBL3360905)
Affinity DataIC50: 7.60E+3nMAssay Description:Inhibition of VHR (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031908BDBM50031908(CHEMBL3360906)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031910BDBM50031910(CHEMBL3360908)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 9(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031906BDBM50031906(CHEMBL3360905)
Affinity DataIC50: 1.07E+4nMAssay Description:Inhibition of MEG2 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031905BDBM50031905(CHEMBL3360904)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 5(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031906BDBM50031906(CHEMBL3360905)
Affinity DataIC50: 1.66E+4nMAssay Description:Inhibition of STEP (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031907BDBM50031907(CHEMBL2337245)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031908BDBM50031908(CHEMBL3360906)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031909BDBM50031909(CHEMBL3360907)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetProtein phosphatase 1A(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50343530BDBM50343530(5,7-dichloro-4-((3-(4-methoxyphenylthio)benzyl)(me...)
Affinity DataIC50: 2.10E+4nMAssay Description:Inhibition of PPM1A (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031904BDBM50031904(CHEMBL3360903)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 18(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031906BDBM50031906(CHEMBL3360905)
Affinity DataIC50: 2.64E+4nMAssay Description:Inhibition of PTPN18 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031920BDBM50031920(CHEMBL3360916)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 18(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031910BDBM50031910(CHEMBL3360908)
Affinity DataIC50: 2.97E+4nMAssay Description:Inhibition of PTPN18 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetProtein phosphatase 1A(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031908BDBM50031908(CHEMBL3360906)
Affinity DataIC50: 3.18E+4nMAssay Description:Inhibition of PPM1A (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031913BDBM50031913(CHEMBL3360910)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 9(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031908BDBM50031908(CHEMBL3360906)
Affinity DataIC50: 3.75E+4nMAssay Description:Inhibition of MEG2 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50343530BDBM50343530(5,7-dichloro-4-((3-(4-methoxyphenylthio)benzyl)(me...)
Affinity DataIC50: 3.88E+4nMAssay Description:Inhibition of PTP1B (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031917BDBM50031917(CHEMBL3360913)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031911BDBM50031911(CHEMBL1299903)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031919BDBM50031919(CHEMBL3360915)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031918BDBM50031918(CHEMBL3360914)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031912BDBM50031912(CHEMBL3360909)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetProtein phosphatase 1A(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031910BDBM50031910(CHEMBL3360908)
Affinity DataIC50: 4.25E+4nMAssay Description:Inhibition of PPM1A (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031946BDBM50031946(CHEMBL3360917)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetDual specificity protein phosphatase 3(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031908BDBM50031908(CHEMBL3360906)
Affinity DataIC50: 5.01E+4nMAssay Description:Inhibition of VHR (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetDual specificity protein phosphatase 3(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50343530BDBM50343530(5,7-dichloro-4-((3-(4-methoxyphenylthio)benzyl)(me...)
Affinity DataIC50: 5.07E+4nMAssay Description:Inhibition of VHR (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 5(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50343530BDBM50343530(5,7-dichloro-4-((3-(4-methoxyphenylthio)benzyl)(me...)
Affinity DataIC50: 6.06E+4nMAssay Description:Inhibition of STEP (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031910BDBM50031910(CHEMBL3360908)
Affinity DataIC50: 6.38E+4nMAssay Description:Inhibition of PTP1B (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 9(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50343530BDBM50343530(5,7-dichloro-4-((3-(4-methoxyphenylthio)benzyl)(me...)
Affinity DataIC50: 6.61E+4nMAssay Description:Inhibition of MEG2 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetProtein phosphatase 1A(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031906BDBM50031906(CHEMBL3360905)
Affinity DataIC50: 6.78E+4nMAssay Description:Inhibition of PPM1A (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetProtein phosphatase 1G(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50343530BDBM50343530(5,7-dichloro-4-((3-(4-methoxyphenylthio)benzyl)(me...)
Affinity DataIC50: 7.48E+4nMAssay Description:Inhibition of PPM1G (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 9(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031910BDBM50031910(CHEMBL3360908)
Affinity DataIC50: 7.85E+4nMAssay Description:Inhibition of MEG2 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031914BDBM50031914(CHEMBL3196685)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 5(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031908BDBM50031908(CHEMBL3360906)
Affinity DataIC50: 9.60E+4nMAssay Description:Inhibition of STEP (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50032153BDBM50032153(CHEMBL3360918)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50032156BDBM50032156(CHEMBL3360919)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetProtein phosphatase 1G(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031906BDBM50031906(CHEMBL3360905)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of PPM1G (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 5(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031910BDBM50031910(CHEMBL3360908)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of STEP (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031947BDBM50031947(CHEMBL1363574)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 18(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031908BDBM50031908(CHEMBL3360906)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of PTPN18 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031945BDBM50031945(CHEMBL3352902)
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 Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetProtein phosphatase Slingshot homolog 2(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031910BDBM50031910(CHEMBL3360908)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of SSH2 (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
TargetProtein phosphatase 1G(Human)
Shandong University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50031910BDBM50031910(CHEMBL3360908)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of PPM1G (unknown origin) assessed as reduction in pNPP hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2016
Entry Details Article
PubMed
Displayed 1 to 50 (of 58 total ) | Next | Last >>
Jump to: