BDBM19872 N-(Cyanomethyl)-4-methyl-2-(3-pyrimidin-5-ylphenyl)pentamide::N-(cyanomethyl)-4-methyl-2-[3-(pyrimidin-5-yl)phenyl]pentanamide::Nonpeptidic Biaryl Nitrile Compound, 36

SMILES CC(C)CC(C(=O)NCC#N)c1cccc(c1)-c1cncnc1

InChI Key InChIKey=MADQTLUXXWHNRP-UHFFFAOYSA-N

Data  4 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 4 hits for monomerid = 19872   

TargetCathepsin K(Human)
Merck Frosst Centre For Therapeutic Research

LigandPNGBDBM19872(N-(Cyanomethyl)-4-methyl-2-(3-pyrimidin-5-ylphenyl...)
Affinity DataIC50: 1.04E+3nMpH: 5.5 T: 2°CAssay Description:Prior to the addition of substrate, different concentrations of the inhibitor ranging from 100 uM to 0.2 nM were preincubated for 15 min with enzyme ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetProcathepsin L(Human)
Merck Frosst Centre For Therapeutic Research

LigandPNGBDBM19872(N-(Cyanomethyl)-4-methyl-2-(3-pyrimidin-5-ylphenyl...)
Affinity DataIC50: 1.00E+4nMAssay Description:Prior to the addition of substrate, different concentrations of the inhibitor ranging from 100 uM to 0.2 nM were preincubated for 15 min with enzyme ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetCathepsin S(Human)
Merck Frosst Centre For Therapeutic Research

LigandPNGBDBM19872(N-(Cyanomethyl)-4-methyl-2-(3-pyrimidin-5-ylphenyl...)
Affinity DataIC50: 1.00E+4nMAssay Description:Prior to the addition of substrate, different concentrations of the inhibitor ranging from 100 uM to 0.2 nM were preincubated for 15 min with enzyme ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed
TargetCathepsin B(Human)
Merck Frosst Centre For Therapeutic Research

LigandPNGBDBM19872(N-(Cyanomethyl)-4-methyl-2-(3-pyrimidin-5-ylphenyl...)
Affinity DataIC50: 1.00E+4nMAssay Description:Prior to the addition of substrate, different concentrations of the inhibitor ranging from 100 uM to 0.2 nM were preincubated for 15 min with enzyme ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/6/2008
Entry Details Article
PubMed