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SMILES: COc1ccc2c(c1)oc1cccc(CNCc3ccccc3)c21

InChI Key: InChIKey=PQBKEUKZUAKYBM-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 = 50449400   
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
Cholinesterase


(Equus caballus (Horse))
BDBM50449400
PNG
(CHEMBL3127213)
Show SMILES COc1ccc2c(c1)oc1cccc(CNCc3ccccc3)c21
Show InChI InChI=1S/C21H19NO2/c1-23-17-10-11-18-20(12-17)24-19-9-5-8-16(21(18)19)14-22-13-15-6-3-2-4-7-15/h2-12,22H,13-14H2,1H3
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.81E+4n/an/an/an/an/an/a



Southeast University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 5 ...


Eur J Med Chem 76: 376-86 (2014)


Article DOI: 10.1016/j.ejmech.2014.02.035
BindingDB Entry DOI: 10.7270/Q2W097FT
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50449400
PNG
(CHEMBL3127213)
Show SMILES COc1ccc2c(c1)oc1cccc(CNCc3ccccc3)c21
Show InChI InChI=1S/C21H19NO2/c1-23-17-10-11-18-20(12-17)24-19-9-5-8-16(21(18)19)14-22-13-15-6-3-2-4-7-15/h2-12,22H,13-14H2,1H3
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>5.00E+4n/an/an/an/an/an/a



Southeast University

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 5 m...


Eur J Med Chem 76: 376-86 (2014)


Article DOI: 10.1016/j.ejmech.2014.02.035
BindingDB Entry DOI: 10.7270/Q2W097FT
More data for this
Ligand-Target Pair