BDBM50386354 CHEMBL2048586

SMILES CC1CN(CC(C)O1)c1nnc(s1)N1CCC(CC1)N1CCCCC1

InChI Key InChIKey=BPOGPSWQWXFRCB-UHFFFAOYSA-N

Data  2 KI

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50386354   

TargetHistamine H3 receptor(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50386354(CHEMBL2048586)
Show SMILES CC1CN(CC(C)O1)c1nnc(s1)N1CCC(CC1)N1CCCCC1
Show InChI InChI=1S/C18H31N5OS/c1-14-12-23(13-15(2)24-14)18-20-19-17(25-18)22-10-6-16(7-11-22)21-8-4-3-5-9-21/h14-16H,3-13H2,1-2H3
Affinity DataKi:  35nMAssay Description:Displacement of [3H]-N-alpha-methylhistamine from mouse recombinant histamine H3 receptor after 30 mins by scintillation countingMore data for this Ligand-Target Pair
TargetHistamine H3 receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50386354(CHEMBL2048586)
Show SMILES CC1CN(CC(C)O1)c1nnc(s1)N1CCC(CC1)N1CCCCC1
Show InChI InChI=1S/C18H31N5OS/c1-14-12-23(13-15(2)24-14)18-20-19-17(25-18)22-10-6-16(7-11-22)21-8-4-3-5-9-21/h14-16H,3-13H2,1-2H3
Affinity DataKi:  53nMAssay Description:Displacement of [3H]-N-alpha-methylhistamine from human recombinant histamine H3 receptor after 30 mins by scintillation countingMore data for this Ligand-Target Pair