BindingDB logo
myBDB logout

null

SMILES: N=C(NCCCc1cnc[nH]1)NCC1CCCCC1

InChI Key: InChIKey=WMFPMYMVNGZFBC-UHFFFAOYSA-N

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50283867   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Histamine H3 receptor


(GUINEA PIG)
BDBM50283867
PNG
(CHEMBL98165 | N-Cyclohexylmethyl-N'-[3-(1H-imidazo...)
Show SMILES N=C(NCCCc1cnc[nH]1)NCC1CCCCC1
Show InChI InChI=1S/C14H25N5/c15-14(18-9-12-5-2-1-3-6-12)17-8-4-7-13-10-16-11-19-13/h10-12H,1-9H2,(H,16,19)(H3,15,17,18)
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
0.740n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Antagonistic activity for Histamine H3 receptor binding in guinea pig


Bioorg Med Chem Lett 4: 2907-2912 (1994)


Article DOI: 10.1016/S0960-894X(01)80838-6
BindingDB Entry DOI: 10.7270/Q20K28H8
More data for this
Ligand-Target Pair
Histamine H3 receptor


(GUINEA PIG)
BDBM50283867
PNG
(CHEMBL98165 | N-Cyclohexylmethyl-N'-[3-(1H-imidazo...)
Show SMILES N=C(NCCCc1cnc[nH]1)NCC1CCCCC1
Show InChI InChI=1S/C14H25N5/c15-14(18-9-12-5-2-1-3-6-12)17-8-4-7-13-10-16-11-19-13/h10-12H,1-9H2,(H,16,19)(H3,15,17,18)
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
0.794n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Antagonistic activity for Histamine H3 receptor on electrically evoked guinea-pig ileum contraction


Bioorg Med Chem Lett 4: 2907-2912 (1994)


Article DOI: 10.1016/S0960-894X(01)80838-6
BindingDB Entry DOI: 10.7270/Q20K28H8
More data for this
Ligand-Target Pair