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BDBM50333159 5-Amino-7-benzyl-2-chloro-6,7,8,9-tetrahydropyrido[2,3-b][1,6]naphthyridin-3-carbonitrile::CHEMBL1644818

SMILES: Nc1c2CN(Cc3ccccc3)CCc2nc2nc(Cl)c(cc12)C#N

InChI Key: InChIKey=AJSOITFEAIHORD-UHFFFAOYSA-N

Data: 3 IC50

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Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50333159   
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
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50333159
PNG
(5-Amino-7-benzyl-2-chloro-6,7,8,9-tetrahydropyrido...)
Show SMILES Nc1c2CN(Cc3ccccc3)CCc2nc2nc(Cl)c(cc12)C#N
Show InChI InChI=1S/C19H16ClN5/c20-18-13(9-21)8-14-17(22)15-11-25(10-12-4-2-1-3-5-12)7-6-16(15)23-19(14)24-18/h1-5,8H,6-7,10-11H2,(H2,22,23,24)
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n/an/a 350n/an/an/an/an/an/a



Laboratorio de Radicales Libres y Qu�mica Computacional (IQOG, CSIC)

Curated by ChEMBL


Assay Description
Inhibition of Electrophorus electricus AChE by Ellman's method


Bioorg Med Chem 19: 122-33 (2011)


Article DOI: 10.1016/j.bmc.2010.11.040
BindingDB Entry DOI: 10.7270/Q22R3RX5
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50333159
PNG
(5-Amino-7-benzyl-2-chloro-6,7,8,9-tetrahydropyrido...)
Show SMILES Nc1c2CN(Cc3ccccc3)CCc2nc2nc(Cl)c(cc12)C#N
Show InChI InChI=1S/C19H16ClN5/c20-18-13(9-21)8-14-17(22)15-11-25(10-12-4-2-1-3-5-12)7-6-16(15)23-19(14)24-18/h1-5,8H,6-7,10-11H2,(H2,22,23,24)
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n/an/a>1.00E+5n/an/an/an/an/an/a



Laboratorio de Radicales Libres y Qu�mica Computacional (IQOG, CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE by Ellman's method


Bioorg Med Chem 19: 122-33 (2011)


Article DOI: 10.1016/j.bmc.2010.11.040
BindingDB Entry DOI: 10.7270/Q22R3RX5
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Bos taurus (bovine))
BDBM50333159
PNG
(5-Amino-7-benzyl-2-chloro-6,7,8,9-tetrahydropyrido...)
Show SMILES Nc1c2CN(Cc3ccccc3)CCc2nc2nc(Cl)c(cc12)C#N
Show InChI InChI=1S/C19H16ClN5/c20-18-13(9-21)8-14-17(22)15-11-25(10-12-4-2-1-3-5-12)7-6-16(15)23-19(14)24-18/h1-5,8H,6-7,10-11H2,(H2,22,23,24)
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n/an/a>1.00E+5n/an/an/an/an/an/a



Laboratorio de Radicales Libres y Qu�mica Computacional (IQOG, CSIC)

Curated by ChEMBL


Assay Description
Inhibition of bovine erythrocytes AChE by Ellman's method


Bioorg Med Chem 19: 122-33 (2011)


Article DOI: 10.1016/j.bmc.2010.11.040
BindingDB Entry DOI: 10.7270/Q22R3RX5
More data for this
Ligand-Target Pair