BDBM50119708 2-Cyano-N-{(S)-1-[3-(4-cyclopropanecarbonyl-phenoxy)-propyl]-pyrrolidin-3-yl}-benzenesulfonamide::CHEMBL420108

SMILES O=C(C1CC1)c1ccc(OCCCN2CC[C@@H](C2)NS(=O)(=O)c2ccccc2C#N)cc1

InChI Key InChIKey=QFTNRJFCJNHEPW-NRFANRHFSA-N

Data  3 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50119708   

TargetHistamine H3 receptor(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50119708(2-Cyano-N-{(S)-1-[3-(4-cyclopropanecarbonyl-phenox...)
Affinity DataKi:  11nMAssay Description:Binding affinity against rat histamine H3 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H2 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50119708(2-Cyano-N-{(S)-1-[3-(4-cyclopropanecarbonyl-phenox...)
Affinity DataKi:  710nMAssay Description:Binding affinity to the human Histamine H2 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H1 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50119708(2-Cyano-N-{(S)-1-[3-(4-cyclopropanecarbonyl-phenox...)
Affinity DataKi:  6.20E+3nMAssay Description:Binding affinity to the human Histamine H1 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed