BDBM50097380 CHEMBL3586432

SMILES [H][C@@]12CN(C[C@]1([H])CN(C2)c1nc(C)cc(C)n1)C(=O)c1ccccc1-n1nccn1

InChI Key InChIKey=LCDKKZMNYHMDCH-UHFFFAOYSA-N

Data  3 KI  1 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50097380   

LigandPNGBDBM50097380(CHEMBL3586432)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of [3H]-astemizole binding to human ERG expressed in HEK293 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2016
Entry Details Article
PubMed
TargetOrexin receptor type 2(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50097380(CHEMBL3586432)
Affinity DataKi:  2nMAssay Description:Binding affinity to rat OX2 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2016
Entry Details Article
PubMed
TargetOrexin receptor type 2(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50097380(CHEMBL3586432)
Affinity DataKi:  12nMAssay Description:Binding affinity to human OX2 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2016
Entry Details Article
PubMed
TargetOrexin/Hypocretin receptor type 1(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50097380(CHEMBL3586432)
Affinity DataKi:  1.64E+3nMAssay Description:Binding affinity to human OX1 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2016
Entry Details Article
PubMed