BindingDB logo
myBDB logout
Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Acetylcholinesterase' and Ligand = 'BDBM50004003'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50004003
PNG
(2-(2-(1-benzylpiperidin-4-yl)ethyl)-3,4-dihydroiso...)
Show SMILES O=C1N(CCC2CCN(Cc3ccccc3)CC2)CCc2ccccc12
Show InChI InChI=1S/C23H28N2O/c26-23-22-9-5-4-8-21(22)13-17-25(23)16-12-19-10-14-24(15-11-19)18-20-6-2-1-3-7-20/h1-9,19H,10-18H2
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 1.00E+3n/an/an/an/an/an/a



Sichuan University

Curated by ChEMBL


Assay Description
Inhibition of AChE


Eur J Med Chem 45: 1167-72 (2010)


Article DOI: 10.1016/j.ejmech.2009.12.038
BindingDB Entry DOI: 10.7270/Q25H7GFM
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Mus musculus (mouse))
BDBM50004003
PNG
(2-(2-(1-benzylpiperidin-4-yl)ethyl)-3,4-dihydroiso...)
Show SMILES O=C1N(CCC2CCN(Cc3ccccc3)CC2)CCc2ccccc12
Show InChI InChI=1S/C23H28N2O/c26-23-22-9-5-4-8-21(22)13-17-25(23)16-12-19-10-14-24(15-11-19)18-20-6-2-1-3-7-20/h1-9,19H,10-18H2
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 1.00E+3n/an/an/an/an/an/a



Eisai Co., Ltd.

Curated by ChEMBL


Assay Description
In vitro inhibitory concentration against acetylcholinesterase (AChE) obtained from mouse brain homogenate.


J Med Chem 35: 4542-8 (1993)


Article DOI: 10.1021/jm00102a005
BindingDB Entry DOI: 10.7270/Q25M64P8
More data for this
Ligand-Target Pair