BDBM50364171 CHEMBL1951598

SMILES [#6]-[#8]-c1cccc(c1)-[#6](=O)-[#6]-n1c(=O)n(-[#6])c2c(C#N)c(-[#7]-3-[#6]-[#6]-[#6]-[#6@H](-[#7])-[#6]-3)n(-[#6]\[#6]=[#6](\[#6])-[#6])c2c1=O

InChI Key InChIKey=YWUJRVWUHMSTRQ-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50364171   

TargetDipeptidyl peptidase 4(Human)
Argenta Discovery

Curated by ChEMBL
LigandPNGBDBM50364171(CHEMBL1951598)
Affinity DataIC50: 0.5nMAssay Description:Inhibition of human C-terminal step-tagged DPP4 expressed using baculovirus systemMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/23/2012
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Argenta Discovery

Curated by ChEMBL
LigandPNGBDBM50364171(CHEMBL1951598)
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of human ERG by dofetilide binding assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/23/2012
Entry Details Article
PubMed
TargetMuscarinic acetylcholine receptor M1(Human)
Argenta Discovery

Curated by ChEMBL
LigandPNGBDBM50364171(CHEMBL1951598)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of M1 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/23/2012
Entry Details Article
PubMed