BDBM50103449 CHEMBL3398248

SMILES CCNc1cc(cc2SSSSSc12)C(F)(F)F

InChI Key InChIKey=XDMLQTPNUBVWFJ-UHFFFAOYSA-N

Data  1 KI  2 IC50

  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 3 hits for monomerid = 50103449   

TargetTyrosine-protein phosphatase non-receptor type 5(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50103449(CHEMBL3398248)
Affinity DataKi:  230nMAssay Description:Inhibition of STEP (unknown origin) in absence of GSH by p-nitrophenyl phosphate hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 5(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50103449(CHEMBL3398248)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of STEP (unknown origin) pre-incubated for 10 mins before addition of p-nitrophenyl phosphate substrate in presence of 1 mM GSHMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 5(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50103449(CHEMBL3398248)
Affinity DataIC50:  59nMAssay Description:Inhibition of STEP (unknown origin) pre-incubated for 10 mins before addition of p-nitrophenyl phosphate substrate in absence of GSHMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed