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BDBM50358533 CHEMBL1923522

SMILES: CN1CCN(CC1)c1nc(N2CCCC2)c2cnn(C)c2n1

InChI Key: InChIKey=DFBFDRZHAVAEKE-UHFFFAOYSA-N

Data: 2 KI

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 = 50358533   
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 H1 receptor


(Homo sapiens (Human))
BDBM50358533
PNG
(CHEMBL1923522)
Show SMILES CN1CCN(CC1)c1nc(N2CCCC2)c2cnn(C)c2n1
Show InChI InChI=1S/C15H23N7/c1-19-7-9-22(10-8-19)15-17-13-12(11-16-20(13)2)14(18-15)21-5-3-4-6-21/h11H,3-10H2,1-2H3
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CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
62n/an/an/an/an/an/an/an/a



VU University Amsterdam

Curated by ChEMBL


Assay Description
Displacement of [3H]mepyramine from human histamine H1 receptor expressed in HEK293 cells after 1 to 1.5 hrs by scintillation counting


J Med Chem 54: 8195-206 (2011)


Article DOI: 10.1021/jm2011589
BindingDB Entry DOI: 10.7270/Q2QF8T85
More data for this
Ligand-Target Pair
Histamine H4 receptor


(Homo sapiens (Human))
BDBM50358533
PNG
(CHEMBL1923522)
Show SMILES CN1CCN(CC1)c1nc(N2CCCC2)c2cnn(C)c2n1
Show InChI InChI=1S/C15H23N7/c1-19-7-9-22(10-8-19)15-17-13-12(11-16-20(13)2)14(18-15)21-5-3-4-6-21/h11H,3-10H2,1-2H3
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
2.90E+3n/an/an/an/an/an/an/an/a



VU University Amsterdam

Curated by ChEMBL


Assay Description
Displacement of [3H]histamine from human histamine H4 receptor expressed in HEK293 cells after 1 to 1.5 hrs by scintillation counting


J Med Chem 54: 8195-206 (2011)


Article DOI: 10.1021/jm2011589
BindingDB Entry DOI: 10.7270/Q2QF8T85
More data for this
Ligand-Target Pair