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BDBM50110302 Acridin-9-yl-(3-piperidin-1-yl-propyl)-amine; Oxalic acid::CHEMBL277988

SMILES: C(CNc1c2ccccc2nc2ccccc12)CN1CCCCC1

InChI Key: InChIKey=NXTOUTQSWQTEPN-UHFFFAOYSA-N

Data: 1 KI  1 IC50

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   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50110302   
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))
BDBM50110302
PNG
(Acridin-9-yl-(3-piperidin-1-yl-propyl)-amine; Oxal...)
Show SMILES C(CNc1c2ccccc2nc2ccccc12)CN1CCCCC1
Show InChI InChI=1S/C21H25N3/c1-6-14-24(15-7-1)16-8-13-22-21-17-9-2-4-11-19(17)23-20-12-5-3-10-18(20)21/h2-5,9-12H,1,6-8,13-16H2,(H,22,23)
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
188n/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)
BDBM50110302
PNG
(Acridin-9-yl-(3-piperidin-1-yl-propyl)-amine; Oxal...)
Show SMILES C(CNc1c2ccccc2nc2ccccc12)CN1CCCCC1
Show InChI InChI=1S/C21H25N3/c1-6-14-24(15-7-1)16-8-13-22-21-17-9-2-4-11-19(17)23-20-12-5-3-10-18(20)21/h2-5,9-12H,1,6-8,13-16H2,(H,22,23)
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 110n/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