BDBM31893 Pyrano[3,2-c]quinoline-6-chlorotacrine hybrid, 18.2HCl

SMILES Clc1ccc(cc1)-c1nc2ccc(cc2c2OCCCc12)C(=O)NCCCCCCNc1c2CCCCc2nc2cc(Cl)ccc12

InChI Key InChIKey=WKWQTNVUORLIAM-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 31893   

TargetAcetylcholinesterase(Human)
Universitat De Barcelona

LigandPNGBDBM31893(Pyrano[3,2-c]quinoline-6-chlorotacrine hybrid, 18....)
Affinity DataIC50: 19.2nMpH: 8.0 T: 2°CAssay Description:AChE inhibitory activity was evaluated spectrophotometrically by the method of Ellman, using AChE from bovine or human erythrocytes and acetylthiocho...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/28/2009
Entry Details Article
PubMed
TargetAcetylcholinesterase(Bovine)
Universitat De Barcelona

LigandPNGBDBM31893(Pyrano[3,2-c]quinoline-6-chlorotacrine hybrid, 18....)
Affinity DataIC50: 20.4nMpH: 8.0 T: 2°CAssay Description:AChE inhibitory activity was evaluated spectrophotometrically by the method of Ellman, using AChE from bovine or human erythrocytes and acetylthiocho...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/28/2009
Entry Details Article
PubMed
TargetCholinesterase(Human)
Universitat De Barcelona

LigandPNGBDBM31893(Pyrano[3,2-c]quinoline-6-chlorotacrine hybrid, 18....)
Affinity DataIC50: 1.07E+3nMpH: 8.0 T: 2°CAssay Description:BChE inhibitory activity was evaluated spectrophotometrically by the method of Ellman, using BChE from human serum and butyrylthiocholine as substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/28/2009
Entry Details Article
PubMed