BDBM50097379 CHEMBL3586437

SMILES [H][C@@]12CN(C[C@]1([H])CN(C2)c1nc(C)cc(C)n1)C(=O)c1ccccc1-c1ncn[nH]1

InChI Key InChIKey=NYDBXNHNMPHNGA-UHFFFAOYSA-N

Data  3 KI  1 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 4 hits for monomerid = 50097379   

TargetOrexin receptor type 2(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50097379(CHEMBL3586437)
Affinity DataKi:  30nMAssay 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 receptor type 2(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50097379(CHEMBL3586437)
Affinity DataKi:  39nMAssay 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/Hypocretin receptor type 1(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50097379(CHEMBL3586437)
Affinity DataKi:  3.65E+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
LigandPNGBDBM50097379(CHEMBL3586437)
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