BDBM12191 (2S)-2-amino-2-cyclohexyl-1-(pyrrolidin-1-yl)ethan-1-one::(S)-2-Amino-2-cyclohexyl-1-pyrrolidin-1-yl-ethanone::(S)-2-amino-2-cyclohexyl-1-(pyrrolidin-1-yl)ethanone::CHEMBL278393::isoquinoline derivative 14

SMILES N[C@@H](C1CCCCC1)C(=O)N1CCCC1

InChI Key InChIKey=RWNSISJNBAQNTF-NSHDSACASA-N

Data  2 KI  8 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 10 hits for monomerid = 12191   

TargetDipeptidyl peptidase 4(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM12191((2S)-2-amino-2-cyclohexyl-1-(pyrrolidin-1-yl)ethan...)
Affinity DataKi:  64nMAssay Description:In vitro test for inhibitory activity against human dipeptidyl peptidase IV.More data for this Ligand-Target Pair
In DepthDetails Article
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM12191((2S)-2-amino-2-cyclohexyl-1-(pyrrolidin-1-yl)ethan...)
Affinity DataKi:  121nMAssay Description:Inhibitory constant against Dipeptidylpeptidase IV activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 2(Homo sapiens (Human))
National Health Research Institutes

LigandPNGBDBM12191((2S)-2-amino-2-cyclohexyl-1-(pyrrolidin-1-yl)ethan...)
Affinity DataIC50: >1.00E+5nMAssay 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 DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM12191((2S)-2-amino-2-cyclohexyl-1-(pyrrolidin-1-yl)ethan...)
Affinity DataIC50:  320nMAssay Description:Inhibitory activity against dipeptidyl-peptidase IV.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM12191((2S)-2-amino-2-cyclohexyl-1-(pyrrolidin-1-yl)ethan...)
Affinity DataIC50:  320nMAssay Description:Inhibitory activity against human Dipeptidyl-peptidase IVMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 2(Homo sapiens (Human))
National Health Research Institutes

LigandPNGBDBM12191((2S)-2-amino-2-cyclohexyl-1-(pyrrolidin-1-yl)ethan...)
Affinity DataIC50:  1.90E+4nMAssay Description:Inhibitory activity against human quiescent cell proline dipeptidase (QPP) enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM12191((2S)-2-amino-2-cyclohexyl-1-(pyrrolidin-1-yl)ethan...)
Affinity DataIC50:  320nMAssay Description:Inhibition of DPP4More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM12191((2S)-2-amino-2-cyclohexyl-1-(pyrrolidin-1-yl)ethan...)
Affinity DataIC50:  1.03E+3nMAssay 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 DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 8(Homo sapiens (Human))
National Health Research Institutes

LigandPNGBDBM12191((2S)-2-amino-2-cyclohexyl-1-(pyrrolidin-1-yl)ethan...)
Affinity DataIC50:  78nMpH: 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 DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 2(Homo sapiens (Human))
National Health Research Institutes

LigandPNGBDBM12191((2S)-2-amino-2-cyclohexyl-1-(pyrrolidin-1-yl)ethan...)
Affinity DataIC50:  1.90E+4nMAssay Description:Inhibitory activity against quiescent cell prolyl peptidase (QPP).More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed