null

SMILES CC12CCC3C(CCC4=CC(=O)CCC34C)C1CCC2C(=O)Cn1cnc2c1nc[nH]c2=S

InChI Key InChIKey=UWSZBXUQILDRMN-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50326558   

TargetReceptor-type tyrosine-protein phosphatase alpha(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50326558(10,13-dimethyl-17-(2-(6-thioxo-3H-purin-9(6H)-yl)a...)copy SMILEScopy InChI
Affinity DataIC50: 3.50E+4nMpH: 7.0Assay Description:Inhibition of human cytoplasmic protein tyrosine phosphatase A assessed as change in enzyme activity at pH 7More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q52QMCPubMed
TargetReceptor-type tyrosine-protein phosphatase beta(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50326558(10,13-dimethyl-17-(2-(6-thioxo-3H-purin-9(6H)-yl)a...)copy SMILEScopy InChI
Affinity DataIC50: 1.35E+5nMpH: 5.0Assay Description:Inhibition of human cytoplasmic protein tyrosine phosphatase B assessed as change in enzyme activity at pH 5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q52QMCPubMed
TargetReceptor-type tyrosine-protein phosphatase alpha(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50326558(10,13-dimethyl-17-(2-(6-thioxo-3H-purin-9(6H)-yl)a...)copy SMILEScopy InChI
Affinity DataIC50: 9.30E+4nMpH: 5.0Assay Description:Inhibition of human cytoplasmic protein tyrosine phosphatase A assessed as change in enzyme activity at pH 5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q52QMCPubMed