BDBM12190 (2S)-2-amino-2-cyclohexyl-1-(piperidin-1-yl)ethan-1-one::isoquinoline derivative 13

SMILES N[C@@H](C1CCCCC1)C(=O)N1CCCCC1

InChI Key InChIKey=VDESQGCBPRUBON-UHFFFAOYSA-N

Data  3 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 = 12190   

TargetDipeptidyl peptidase 8(Human)
National Health Research Institutes

LigandPNGBDBM12190((2S)-2-amino-2-cyclohexyl-1-(piperidin-1-yl)ethan-...)
Affinity DataIC50: 1.45E+3nMpH: 8.0 T: 2°CAssay Description:The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/27/2006
Entry Details Article
PubMed
TargetDipeptidyl peptidase 2(Human)
National Health Research Institutes

LigandPNGBDBM12190((2S)-2-amino-2-cyclohexyl-1-(piperidin-1-yl)ethan-...)
Affinity DataIC50: 2.74E+4nMAssay Description:The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/27/2006
Entry Details Article
PubMed
TargetDipeptidyl peptidase 4(Human)
National Health Research Institutes

LigandPNGBDBM12190((2S)-2-amino-2-cyclohexyl-1-(piperidin-1-yl)ethan-...)
Affinity DataIC50: 3.10E+4nMAssay Description:The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/27/2006
Entry Details Article
PubMed