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SMILES: C([C@H]1CCCN2CCCC[C@H]12)N1c2ccccc2[Se]c2ccccc12

InChI Key: InChIKey=HQEXJFWZSQNDAX-QZTJIDSGSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50346429   
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))		BDBM50346429
PNG
(10-(((1R,9aR)-octahydro-1H-quinolizin-1-yl)methyl)...)
Show SMILES C([C@H]1CCCN2CCCC[C@H]12)N1c2ccccc2[Se]c2ccccc12 |r|
Show InChI InChI=1S/C22H26N2Se/c1-3-12-21-19(10-1)24(20-11-2-4-13-22(20)25-21)16-17-8-7-15-23-14-6-5-9-18(17)23/h1-4,10-13,17-18H,5-9,14-16H2/t17-,18-/m1/s1
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Similars
Article
PubMed
n/an/a 870n/an/an/an/an/an/a



Universit£ degli Studi di Genova

Curated by ChEMBL


Assay Description
Inhibition of Equine serum BChE using butyrylthiocoline iodide as a substrate after 20 mins by Ellman's assay

Eur J Med Chem 46: 2170-84 (2011)


Article DOI: 10.1016/j.ejmech.2011.02.071
BindingDB Entry DOI: 10.7270/Q2BK1CPG
More data for this
Ligand-Target Pair