BDBM50215329 (3R,4R)-1-([1,2,4]triazolo[4,3-a]pyrimidin-7-yl)-4-(2,4,5-trifluorophenyl)piperidin-3-aminium 2,2,2-trifluoroacetate::CHEMBL231294

SMILES [NH3+][C@H]1CN(CC[C@@H]1c1cc(F)c(F)cc1F)c1ccn2cnnc2n1

InChI Key InChIKey=BVGLFSCRZQKKNX-UHFFFAOYSA-O

Data  6 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 6 hits for monomerid = 50215329   

TargetDipeptidyl peptidase 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50215329((3R,4R)-1-([1,2,4]triazolo[4,3-a]pyrimidin-7-yl)-4...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of QPPMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetDipeptidyl peptidase 4(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50215329((3R,4R)-1-([1,2,4]triazolo[4,3-a]pyrimidin-7-yl)-4...)
Affinity DataIC50: 26nMAssay Description:Inhibition of DPP4More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetDipeptidyl peptidase 9(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50215329((3R,4R)-1-([1,2,4]triazolo[4,3-a]pyrimidin-7-yl)-4...)
Affinity DataIC50: 4.30E+4nMAssay Description:Inhibition of DPP9More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCytochrome P450 2D6(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50215329((3R,4R)-1-([1,2,4]triazolo[4,3-a]pyrimidin-7-yl)-4...)
Affinity DataIC50: 2.06E+4nMAssay Description:Inhibition of Cyp2D6More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetDipeptidyl peptidase 8(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50215329((3R,4R)-1-([1,2,4]triazolo[4,3-a]pyrimidin-7-yl)-4...)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of DPP8More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50215329((3R,4R)-1-([1,2,4]triazolo[4,3-a]pyrimidin-7-yl)-4...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human ERG potassium channelMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed