BindingDB logo
myBDB logout

null

SMILES: CN(CCCCCCCCN(C)c1cc2nc(nn(-c3ccccc3)c2cc1=O)-c1ccccc1)Cc1ccccc1

InChI Key: InChIKey=QSCUQGSALNRSCA-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 1 hit for monomerid = 50392584   
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))		BDBM50392584
PNG
(CHEMBL2153024)
Show SMILES CN(CCCCCCCCN(C)c1cc2nc(nn(-c3ccccc3)c2cc1=O)-c1ccccc1)Cc1ccccc1
Show InChI InChI=1S/C36H41N5O/c1-39(28-29-18-10-7-11-19-29)24-16-5-3-4-6-17-25-40(2)34-26-32-33(27-35(34)42)41(31-22-14-9-15-23-31)38-36(37-32)30-20-12-8-13-21-30/h7-15,18-23,26-27H,3-6,16-17,24-25,28H2,1-2H3
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 310n/an/an/an/an/an/a



Universit£ degli Studi di Bari Aldo Moro

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 20 mins by Ellman's method

Eur J Med Chem 58: 84-97 (2012)


Article DOI: 10.1016/j.ejmech.2012.10.003
BindingDB Entry DOI: 10.7270/Q2DR2WMH
More data for this
Ligand-Target Pair