BDBM50119723 CHEMBL430502::N-{(S)-1-[3-(4-Acetyl-phenoxy)-propyl]-pyrrolidin-3-yl}-4-cyano-benzamide

SMILES CC(=O)c1ccc(OCCCN2CC[C@@H](C2)NC(=O)c2ccc(cc2)C#N)cc1

InChI Key InChIKey=QIPPGLRRKJCTOV-UHFFFAOYSA-N

Data  3 KI

  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 = 50119723   

TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50119723(N-{(S)-1-[3-(4-Acetyl-phenoxy)-propyl]-pyrrolidin-...)
Affinity DataKi:  40nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H2 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50119723(N-{(S)-1-[3-(4-Acetyl-phenoxy)-propyl]-pyrrolidin-...)
Affinity DataKi:  6.10E+3nMAssay Description:Binding affinity towards human Histamine H2 receptor (For compound 11)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H1 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50119723(N-{(S)-1-[3-(4-Acetyl-phenoxy)-propyl]-pyrrolidin-...)
Affinity DataKi:  1.30E+4nMAssay Description:Binding affinity to the human Histamine H1 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed