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PubMed code 26212777

Compile data set for download or QSAR
Found 22 hits of Enzyme Inhibition Constant Data   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50110727
PNG
(CHEMBL3605838)
Show SMILES Nc1c2C3CCCCC3Sc2nc2CCCCc12
Show InChI InChI=1S/C15H20N2S/c16-14-9-5-1-3-7-11(9)17-15-13(14)10-6-2-4-8-12(10)18-15/h10,12H,1-8H2,(H2,16,17)
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n/an/a 30n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of Electrophorus electricus AChE pre-incubated for 5 mins before acetylthiocholine iodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM8961
PNG
(1,2,3,4-tetrahydro-9-acridinamine | 1,2,3,4-tetrah...)
Show SMILES Nc1c2CCCCc2nc2ccccc12
Show InChI InChI=1S/C13H14N2/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1,3,5,7H,2,4,6,8H2,(H2,14,15)
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n/an/a 50n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of Electrophorus electricus AChE pre-incubated for 5 mins before acetylthiocholine iodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50279987
PNG
(2,3,5,6,7,8-Hexahydro-1H-cyclopenta[b]quinolin-9-y...)
Show SMILES Nc1c2CCCc2nc2CCCCc12
Show InChI InChI=1S/C12H16N2/c13-12-8-4-1-2-6-10(8)14-11-7-3-5-9(11)12/h1-7H2,(H2,13,14)
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n/an/a 70n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE pre-incubated for 5 mins before butyrylthiocholineiodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50110726
PNG
(CHEMBL3605836)
Show SMILES Nc1c2CCCCc2nc2sccc12
Show InChI InChI=1S/C11H12N2S/c12-10-7-3-1-2-4-9(7)13-11-8(10)5-6-14-11/h5-6H,1-4H2,(H2,12,13)
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n/an/a 110n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE pre-incubated for 5 mins before butyrylthiocholineiodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50279987
PNG
(2,3,5,6,7,8-Hexahydro-1H-cyclopenta[b]quinolin-9-y...)
Show SMILES Nc1c2CCCc2nc2CCCCc12
Show InChI InChI=1S/C12H16N2/c13-12-8-4-1-2-6-10(8)14-11-7-3-5-9(11)12/h1-7H2,(H2,13,14)
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n/an/a 170n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of Electrophorus electricus AChE pre-incubated for 5 mins before acetylthiocholine iodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50110726
PNG
(CHEMBL3605836)
Show SMILES Nc1c2CCCCc2nc2sccc12
Show InChI InChI=1S/C11H12N2S/c12-10-7-3-1-2-4-9(7)13-11-8(10)5-6-14-11/h5-6H,1-4H2,(H2,12,13)
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n/an/a 260n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of Electrophorus electricus AChE pre-incubated for 5 mins before acetylthiocholine iodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM39664
PNG
((6-bromo-1-butyl-2,3-dihydropyrrolo[2,3-b]quinolin...)
Show SMILES CCCCN1CCc2c1nc1ccc(Br)cc1c2N
Show InChI InChI=1S/C15H18BrN3/c1-2-3-7-19-8-6-11-14(17)12-9-10(16)4-5-13(12)18-15(11)19/h4-5,9H,2-3,6-8H2,1H3,(H2,17,18)
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n/an/a 300n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of Electrophorus electricus AChE pre-incubated for 5 mins before acetylthiocholine iodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50110699
PNG
(CHEMBL1531257)
Show SMILES CC(=O)c1c(C)nc2ccccc2c1N
Show InChI InChI=1S/C12H12N2O/c1-7-11(8(2)15)12(13)9-5-3-4-6-10(9)14-7/h3-6H,1-2H3,(H2,13,14)
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n/an/a 320n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of Electrophorus electricus AChE pre-incubated for 5 mins before acetylthiocholine iodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50110727
PNG
(CHEMBL3605838)
Show SMILES Nc1c2C3CCCCC3Sc2nc2CCCCc12
Show InChI InChI=1S/C15H20N2S/c16-14-9-5-1-3-7-11(9)17-15-13(14)10-6-2-4-8-12(10)18-15/h10,12H,1-8H2,(H2,16,17)
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n/an/a 330n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE pre-incubated for 5 mins before butyrylthiocholineiodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50110699
PNG
(CHEMBL1531257)
Show SMILES CC(=O)c1c(C)nc2ccccc2c1N
Show InChI InChI=1S/C12H12N2O/c1-7-11(8(2)15)12(13)9-5-3-4-6-10(9)14-7/h3-6H,1-2H3,(H2,13,14)
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n/an/a 460n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE pre-incubated for 5 mins before butyrylthiocholineiodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50210319
PNG
(4-amino-6-methoxy-2-(trifluoromethyl)quinoline-3-c...)
Show SMILES COc1ccc2nc(c(C#N)c(N)c2c1)C(F)(F)F
Show InChI InChI=1S/C12H8F3N3O/c1-19-6-2-3-9-7(4-6)10(17)8(5-16)11(18-9)12(13,14)15/h2-4H,1H3,(H2,17,18)
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n/an/a 690n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of Electrophorus electricus AChE pre-incubated for 5 mins before acetylthiocholine iodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50110702
PNG
(CHEMBL283841)
Show SMILES Nc1c2CCN(Cc3ccccc3)c2nc2ccccc12
Show InChI InChI=1S/C18H17N3/c19-17-14-8-4-5-9-16(14)20-18-15(17)10-11-21(18)12-13-6-2-1-3-7-13/h1-9H,10-12H2,(H2,19,20)
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n/an/a 740n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of Electrophorus electricus AChE pre-incubated for 5 mins before acetylthiocholine iodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM8961
PNG
(1,2,3,4-tetrahydro-9-acridinamine | 1,2,3,4-tetrah...)
Show SMILES Nc1c2CCCCc2nc2ccccc12
Show InChI InChI=1S/C13H14N2/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1,3,5,7H,2,4,6,8H2,(H2,14,15)
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n/an/a 820n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE pre-incubated for 5 mins before butyrylthiocholineiodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50110728
PNG
(CHEMBL1617348)
Show SMILES CN1CCc2c1nc1c(C)cccc1c2N
Show InChI InChI=1S/C13H15N3/c1-8-4-3-5-9-11(14)10-6-7-16(2)13(10)15-12(8)9/h3-5H,6-7H2,1-2H3,(H2,14,15)
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n/an/a 1.15E+3n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of Electrophorus electricus AChE pre-incubated for 5 mins before acetylthiocholine iodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50110702
PNG
(CHEMBL283841)
Show SMILES Nc1c2CCN(Cc3ccccc3)c2nc2ccccc12
Show InChI InChI=1S/C18H17N3/c19-17-14-8-4-5-9-16(14)20-18-15(17)10-11-21(18)12-13-6-2-1-3-7-13/h1-9H,10-12H2,(H2,19,20)
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n/an/a 2.25E+3n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE pre-incubated for 5 mins before butyrylthiocholineiodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50110722
PNG
(CHEMBL1478435)
Show SMILES CC1(C)CC(=O)c2c(C1)nc1ccccc1c2N
Show InChI InChI=1S/C15H16N2O/c1-15(2)7-11-13(12(18)8-15)14(16)9-5-3-4-6-10(9)17-11/h3-6H,7-8H2,1-2H3,(H2,16,17)
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n/an/a 7.19E+3n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of Electrophorus electricus AChE pre-incubated for 5 mins before acetylthiocholine iodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50110701
PNG
(CHEMBL3605837)
Show SMILES Nc1c2CCCc2nc2c3CCCc3nn12
Show InChI InChI=1S/C12H14N4/c13-11-7-3-1-5-9(7)14-12-8-4-2-6-10(8)15-16(11)12/h1-6,13H2
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n/an/a 7.41E+3n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of Electrophorus electricus AChE pre-incubated for 5 mins before acetylthiocholine iodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM39664
PNG
((6-bromo-1-butyl-2,3-dihydropyrrolo[2,3-b]quinolin...)
Show SMILES CCCCN1CCc2c1nc1ccc(Br)cc1c2N
Show InChI InChI=1S/C15H18BrN3/c1-2-3-7-19-8-6-11-14(17)12-9-10(16)4-5-13(12)18-15(11)19/h4-5,9H,2-3,6-8H2,1H3,(H2,17,18)
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n/an/a 8.92E+3n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE pre-incubated for 5 mins before butyrylthiocholineiodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50110728
PNG
(CHEMBL1617348)
Show SMILES CN1CCc2c1nc1c(C)cccc1c2N
Show InChI InChI=1S/C13H15N3/c1-8-4-3-5-9-11(14)10-6-7-16(2)13(10)15-12(8)9/h3-5H,6-7H2,1-2H3,(H2,14,15)
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n/an/a 1.59E+4n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE pre-incubated for 5 mins before butyrylthiocholineiodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50210319
PNG
(4-amino-6-methoxy-2-(trifluoromethyl)quinoline-3-c...)
Show SMILES COc1ccc2nc(c(C#N)c(N)c2c1)C(F)(F)F
Show InChI InChI=1S/C12H8F3N3O/c1-19-6-2-3-9-7(4-6)10(17)8(5-16)11(18-9)12(13,14)15/h2-4H,1H3,(H2,17,18)
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n/an/a 3.07E+4n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE pre-incubated for 5 mins before butyrylthiocholineiodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50110722
PNG
(CHEMBL1478435)
Show SMILES CC1(C)CC(=O)c2c(C1)nc1ccccc1c2N
Show InChI InChI=1S/C15H16N2O/c1-15(2)7-11-13(12(18)8-15)14(16)9-5-3-4-6-10(9)17-11/h3-6H,7-8H2,1-2H3,(H2,16,17)
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n/an/a 3.62E+4n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE pre-incubated for 5 mins before butyrylthiocholineiodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))
BDBM50110701
PNG
(CHEMBL3605837)
Show SMILES Nc1c2CCCc2nc2c3CCCc3nn12
Show InChI InChI=1S/C12H14N4/c13-11-7-3-1-5-9(7)14-12-8-4-2-6-10(8)15-16(11)12/h1-6,13H2
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n/an/a 6.09E+4n/an/an/an/an/an/a



Nanjing University of Chinese Medicine

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE pre-incubated for 5 mins before butyrylthiocholineiodide substrate addition by Ellman's method


Bioorg Med Chem Lett 25: 3442-6 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.026
BindingDB Entry DOI: 10.7270/Q22B90TV
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%