BDBM50356859 CHEMBL1915048

SMILES CN[C@@H]1CCN(C1)c1nc(N)nc2c3cc(Cl)cnc3oc12

InChI Key InChIKey=QCLILBHBGZEDKK-UHFFFAOYSA-N

Data  3 KI  1 IC50

  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 4 hits for monomerid = 50356859   

TargetPotassium voltage-gated channel subfamily H member 2(Human)
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50356859(CHEMBL1915048)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human ERG by binding assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/21/2012
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Janssen Research and Development

Curated by ChEMBL
LigandPNGBDBM50356859(CHEMBL1915048)
Affinity DataKi:  9nMAssay Description:Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/7/2015
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Janssen Research and Development

Curated by ChEMBL
LigandPNGBDBM50356859(CHEMBL1915048)
Affinity DataKi:  9nMAssay Description:Displacement of [3H]histamine from human recombinant histamine H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/3/2016
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Janssen Research and Development

Curated by ChEMBL
LigandPNGBDBM50356859(CHEMBL1915048)
Affinity DataKi:  9.40nMAssay Description:Displacement of [3H]histamine from recombinant human histamine H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/21/2012
Entry Details Article
PubMed