BindingDB logo
myBDB logout

BDBM50110298 CHEMBL277113::Ethyl-(3-piperidin-1-yl-propyl)-quinolin-4-yl-amine; Oxalic acid

SMILES: CCN(CCCN1CCCCC1)c1ccnc2ccccc12

InChI Key: InChIKey=IHXVMTQOYIUZHB-UHFFFAOYSA-N

Data: 1 KI  1 IC50

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 = 50110298   
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


(Homo sapiens (Human))
BDBM50110298
PNG
(CHEMBL277113 | Ethyl-(3-piperidin-1-yl-propyl)-qui...)
Show SMILES CCN(CCCN1CCCCC1)c1ccnc2ccccc12
Show InChI InChI=1S/C19H27N3/c1-2-22(16-8-15-21-13-6-3-7-14-21)19-11-12-20-18-10-5-4-9-17(18)19/h4-5,9-12H,2-3,6-8,13-16H2,1H3
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
1.13E+3n/an/an/an/an/an/an/an/a



Freie Universität Berlin

Curated by ChEMBL


Assay Description
Affinity for displacement of [125I]-iodoproxyfan from human histamine H3 receptors stably expressed in CHO cells


J Med Chem 45: 1128-41 (2002)


BindingDB Entry DOI: 10.7270/Q2H70F4V
More data for this
Ligand-Target Pair
Histamine N-methyltransferase


(Rattus norvegicus)
BDBM50110298
PNG
(CHEMBL277113 | Ethyl-(3-piperidin-1-yl-propyl)-qui...)
Show SMILES CCN(CCCN1CCCCC1)c1ccnc2ccccc12
Show InChI InChI=1S/C19H27N3/c1-2-22(16-8-15-21-13-6-3-7-14-21)19-11-12-20-18-10-5-4-9-17(18)19/h4-5,9-12H,2-3,6-8,13-16H2,1H3
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 49n/an/an/an/an/an/a



Freie Universität Berlin

Curated by ChEMBL


Assay Description
Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methylhistamine


J Med Chem 45: 1128-41 (2002)


BindingDB Entry DOI: 10.7270/Q2H70F4V
More data for this
Ligand-Target Pair