BDBM50321470 (6-(3-chlorophenoxy)pyridin-3-yl)(4-cyclopropyl-1,4-diazepan-1-yl)methanone::CHEMBL1171001

SMILES Clc1cccc(Oc2ccc(cn2)C(=O)N2CCCN(CC2)C2CC2)c1

InChI Key InChIKey=SASIOZSVIDJSAI-UHFFFAOYSA-N

Data  2 KI  1 Kd

  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 = 50321470   

TargetHistamine H3 receptor(Rat)
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50321470((6-(3-chlorophenoxy)pyridin-3-yl)(4-cyclopropyl-1,...)
Affinity DataKd:  11.5nMAssay Description:Antagonist activity at rat histamine H3 receptor expressed in human SK-N-MC cells assessed as inhibition of forskolin-induced cAMP accumulation after...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/31/2012
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50321470((6-(3-chlorophenoxy)pyridin-3-yl)(4-cyclopropyl-1,...)
Affinity DataKi:  17nMAssay Description:Displacement of [125I]-iodoproxyfan from human recombinant histamine H3 receptor expressed in human SK-N-MC cells after 1 hr by scintillation countin...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/31/2012
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50321470((6-(3-chlorophenoxy)pyridin-3-yl)(4-cyclopropyl-1,...)
Affinity DataKi:  75nMAssay Description:Binding affinity to histamine H3 receptor in rat brainMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/31/2012
Entry Details Article
PubMed