BDBM50496264 CHEMBL3127692

SMILES CC(C)S(=O)(=O)N1CCC2(CCN(C2)C(=O)N2CCCN(CC2)C2CCC2)CC1

InChI Key InChIKey=BNEMFTSNVXZPSV-UHFFFAOYSA-N

Data  2 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 2 hits for monomerid = 50496264   

TargetHistamine H3 receptor(Homo sapiens (Human))
Astrazeneca

Curated by ChEMBL
LigandPNGBDBM50496264(CHEMBL3127692)
Affinity DataIC50:  3.20nMAssay Description:Antagonist activity at human histamine H3 receptor long form expressed in CHOK1 cells assessed as inhibition of R-alpha-methylhistamine-induced [35S]...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Astrazeneca

Curated by ChEMBL
LigandPNGBDBM50496264(CHEMBL3127692)
Affinity DataIC50: >3.30E+4nMAssay Description:Inhibition of human ERG expressed in CHOK1 cells by electrophysiological analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed