BDBM50031906 CHEMBL3360905

SMILES CCOC(=O)C1=C(C)N=c2s\c(=C\c3ccc(OCc4ccc(cc4)C(O)=O)cc3)c(=O)n2C1c1ccc(cc1)N(C)C

InChI Key InChIKey=DZZGCYCFYKRHAI-OVVQPSECSA-N

Data  1 KI  9 IC50  1 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 11 hits for monomerid = 50031906   

TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(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 DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 5(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(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 DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 9(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(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 DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(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 DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(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 DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(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 DepthDetails ArticlePubMed
TargetProtein phosphatase 1A(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(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 DepthDetails ArticlePubMed
TargetProtein phosphatase 1G(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(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 DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(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 DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 18(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(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 DepthDetails ArticlePubMed
TargetProtein phosphatase Slingshot homolog 2(Homo sapiens (Human))
Shandong University

Curated by ChEMBL
LigandPNGBDBM50031906(CHEMBL3360905)
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 ArticlePubMed