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PubMed code 21429752

Compile data set for download or QSAR
Found 72 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


(Homo sapiens (Human))
BDBM8963
PNG
(CHEMBL32823 | Homodimeric Tacrine Analog 3b | N-[7...)
Show SMILES C(CCCNc1c2CCCCc2nc2ccccc12)CCCNc1c2CCCCc2nc2ccccc12
Show InChI InChI=1S/C33H40N4/c1(2-12-22-34-32-24-14-4-8-18-28(24)36-29-19-9-5-15-25(29)32)3-13-23-35-33-26-16-6-10-20-30(26)37-31-21-11-7-17-27(31)33/h4,6,8,10,14,16,18,20H,1-3,5,7,9,11-13,15,17,19,21-23H2,(H,34,36)(H,35,37)
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n/an/a 4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM8963
PNG
(CHEMBL32823 | Homodimeric Tacrine Analog 3b | N-[7...)
Show SMILES C(CCCNc1c2CCCCc2nc2ccccc12)CCCNc1c2CCCCc2nc2ccccc12
Show InChI InChI=1S/C33H40N4/c1(2-12-22-34-32-24-14-4-8-18-28(24)36-29-19-9-5-15-25(29)32)3-13-23-35-33-26-16-6-10-20-30(26)37-31-21-11-7-17-27(31)33/h4,6,8,10,14,16,18,20H,1-3,5,7,9,11-13,15,17,19,21-23H2,(H,34,36)(H,35,37)
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n/an/a 10n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(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 19n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Acetylcholinesterase


(Homo sapiens (Human))
BDBM8960
PNG
((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)
Show SMILES COc1cc2CC(CC3CCN(Cc4ccccc4)CC3)C(=O)c2cc1OC
Show InChI InChI=1S/C24H29NO3/c1-27-22-14-19-13-20(24(26)21(19)15-23(22)28-2)12-17-8-10-25(11-9-17)16-18-6-4-3-5-7-18/h3-7,14-15,17,20H,8-13,16H2,1-2H3
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n/an/a 32n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Acetylcholinesterase


(Homo sapiens (Human))
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 93n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50342149
PNG
(2-(4-Methylpiperidin-1-yl)-N-(naphth-1-ylmethyl)py...)
Show SMILES CC1CCN(CC1)c1nccc(NCc2cccc3ccccc23)n1
Show InChI InChI=1S/C21H24N4/c1-16-10-13-25(14-11-16)21-22-12-9-20(24-21)23-15-18-7-4-6-17-5-2-3-8-19(17)18/h2-9,12,16H,10-11,13-15H2,1H3,(H,22,23,24)
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n/an/a 2.20E+3n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50319981
PNG
(2-(4-methylpiperazin-1-yl)-N-(naphthalen-1-ylmethy...)
Show SMILES CN1CCN(CC1)c1nccc(NCc2cccc3ccccc23)n1
Show InChI InChI=1S/C20H23N5/c1-24-11-13-25(14-12-24)20-21-10-9-19(23-20)22-15-17-7-4-6-16-5-2-3-8-18(16)17/h2-10H,11-15H2,1H3,(H,21,22,23)
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n/an/a 2.60E+3n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50319972
PNG
(CHEMBL1082977 | N-benzyl-2-(4-methylpiperidin-1-yl...)
Show SMILES CC1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C17H22N4/c1-14-8-11-21(12-9-14)17-18-10-7-16(20-17)19-13-15-5-3-2-4-6-15/h2-7,10,14H,8-9,11-13H2,1H3,(H,18,19,20)
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n/an/a 3.40E+3n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50342163
PNG
(CHEMBL1766019 | N-Benzyl-2-(4-isopropylpiperazin-1...)
Show SMILES CC(C)N1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C18H25N5/c1-15(2)22-10-12-23(13-11-22)18-19-9-8-17(21-18)20-14-16-6-4-3-5-7-16/h3-9,15H,10-14H2,1-2H3,(H,19,20,21)
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n/an/a 3.40E+3n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM8960
PNG
((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)
Show SMILES COc1cc2CC(CC3CCN(Cc4ccccc4)CC3)C(=O)c2cc1OC
Show InChI InChI=1S/C24H29NO3/c1-27-22-14-19-13-20(24(26)21(19)15-23(22)28-2)12-17-8-10-25(11-9-17)16-18-6-4-3-5-7-18/h3-7,14-15,17,20H,8-13,16H2,1-2H3
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n/an/a 3.60E+3n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM10404
PNG
((1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetrac...)
Show SMILES COc1ccc2CN(C)CC[C@@]34C=C[C@H](O)C[C@@H]3Oc1c24 |r,c:12|
Show InChI InChI=1S/C17H21NO3/c1-18-8-7-17-6-5-12(19)9-14(17)21-16-13(20-2)4-3-11(10-18)15(16)17/h3-6,12,14,19H,7-10H2,1-2H3/t12-,14-,17-/m0/s1
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n/an/a 3.80E+3n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50319978
PNG
(CHEMBL1084210 | N-(naphthalen-1-ylmethyl)-2-(pyrro...)
Show SMILES C(Nc1ccnc(n1)N1CCCC1)c1cccc2ccccc12
Show InChI InChI=1S/C19H20N4/c1-2-9-17-15(6-1)7-5-8-16(17)14-21-18-10-11-20-19(22-18)23-12-3-4-13-23/h1-2,5-11H,3-4,12-14H2,(H,20,21,22)
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n/an/a 5.50E+3n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50319970
PNG
(CHEMBL1086014 | N-benzyl-2-thiomorpholinopyrimidin...)
Show SMILES C(Nc1ccnc(n1)N1CCSCC1)c1ccccc1
Show InChI InChI=1S/C15H18N4S/c1-2-4-13(5-3-1)12-17-14-6-7-16-15(18-14)19-8-10-20-11-9-19/h1-7H,8-12H2,(H,16,17,18)
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n/an/a 6.10E+3n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50342162
PNG
(CHEMBL1766020 | N-Benzyl-2-(4-isopropylpiperidin-1...)
Show SMILES CC(C)C1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C19H26N4/c1-15(2)17-9-12-23(13-10-17)19-20-11-8-18(22-19)21-14-16-6-4-3-5-7-16/h3-8,11,15,17H,9-10,12-14H2,1-2H3,(H,20,21,22)
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n/an/a 6.50E+3n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50342156
PNG
(CHEMBL1766144 | N-Benzyl-2-[4-(4-fluorobenzyl)pipe...)
Show SMILES Fc1ccc(CN2CCN(CC2)c2nccc(NCc3ccccc3)n2)cc1
Show InChI InChI=1S/C22H24FN5/c23-20-8-6-19(7-9-20)17-27-12-14-28(15-13-27)22-24-11-10-21(26-22)25-16-18-4-2-1-3-5-18/h1-11H,12-17H2,(H,24,25,26)
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n/an/a 7.30E+3n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50342145
PNG
(CHEMBL1766018 | N-Benzyl-2-(4-cyclohexylpiperazin-...)
Show SMILES C(Nc1ccnc(n1)N1CCN(CC1)C1CCCCC1)c1ccccc1
Show InChI InChI=1S/C21H29N5/c1-3-7-18(8-4-1)17-23-20-11-12-22-21(24-20)26-15-13-25(14-16-26)19-9-5-2-6-10-19/h1,3-4,7-8,11-12,19H,2,5-6,9-10,13-17H2,(H,22,23,24)
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n/an/a 7.60E+3n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50342154
PNG
(CHEMBL1766146 | N4-Benzyl-N2-(1-benzylpiperidin-4-...)
Show SMILES C(Nc1ccnc(NC2CCN(Cc3ccccc3)CC2)n1)c1ccccc1
Show InChI InChI=1S/C23H27N5/c1-3-7-19(8-4-1)17-25-22-11-14-24-23(27-22)26-21-12-15-28(16-13-21)18-20-9-5-2-6-10-20/h1-11,14,21H,12-13,15-18H2,(H2,24,25,26,27)
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n/an/a 8.20E+3n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50319968
PNG
(CHEMBL1085780 | N-benzyl-2-(pyrrolidin-1-yl)pyrimi...)
Show SMILES C(Nc1ccnc(n1)N1CCCC1)c1ccccc1
Show InChI InChI=1S/C15H18N4/c1-2-6-13(7-3-1)12-17-14-8-9-16-15(18-14)19-10-4-5-11-19/h1-3,6-9H,4-5,10-12H2,(H,16,17,18)
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n/an/a 8.70E+3n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50319977
PNG
(2-(4-methylpiperidin-1-yl)-N-phenethylpyrimidin-4-...)
Show SMILES CC1CCN(CC1)c1nccc(NCCc2ccccc2)n1
Show InChI InChI=1S/C18H24N4/c1-15-9-13-22(14-10-15)18-20-12-8-17(21-18)19-11-7-16-5-3-2-4-6-16/h2-6,8,12,15H,7,9-11,13-14H2,1H3,(H,19,20,21)
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n/an/a 8.80E+3n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50319978
PNG
(CHEMBL1084210 | N-(naphthalen-1-ylmethyl)-2-(pyrro...)
Show SMILES C(Nc1ccnc(n1)N1CCCC1)c1cccc2ccccc12
Show InChI InChI=1S/C19H20N4/c1-2-9-17-15(6-1)7-5-8-16(17)14-21-18-10-11-20-19(22-18)23-12-3-4-13-23/h1-2,5-11H,3-4,12-14H2,(H,20,21,22)
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n/an/a 8.90E+3n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50319973
PNG
(CHEMBL1082978 | N-phenethyl-2-(pyrrolidin-1-yl)pyr...)
Show SMILES C(Cc1ccccc1)Nc1ccnc(n1)N1CCCC1
Show InChI InChI=1S/C16H20N4/c1-2-6-14(7-3-1)8-10-17-15-9-11-18-16(19-15)20-12-4-5-13-20/h1-3,6-7,9,11H,4-5,8,10,12-13H2,(H,17,18,19)
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n/an/a 9.80E+3n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50342158
PNG
(CHEMBL1766142 | N-Benzyl-2-[4-(4-chlorobenzyl)pipe...)
Show SMILES Clc1ccc(CN2CCN(CC2)c2nccc(NCc3ccccc3)n2)cc1
Show InChI InChI=1S/C22H24ClN5/c23-20-8-6-19(7-9-20)17-27-12-14-28(15-13-27)22-24-11-10-21(26-22)25-16-18-4-2-1-3-5-18/h1-11H,12-17H2,(H,24,25,26)
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n/an/a 1.07E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50342154
PNG
(CHEMBL1766146 | N4-Benzyl-N2-(1-benzylpiperidin-4-...)
Show SMILES C(Nc1ccnc(NC2CCN(Cc3ccccc3)CC2)n1)c1ccccc1
Show InChI InChI=1S/C23H27N5/c1-3-7-19(8-4-1)17-25-22-11-14-24-23(27-22)26-21-12-15-28(16-13-21)18-20-9-5-2-6-10-20/h1-11,14,21H,12-13,15-18H2,(H2,24,25,26,27)
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n/an/a 1.24E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50342153
PNG
(4-[4-(benzylamino)pyrimidin-2-yl]thiomorpholine-1-...)
Show SMILES O=S1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C15H18N4OS/c20-21-10-8-19(9-11-21)15-16-7-6-14(18-15)17-12-13-4-2-1-3-5-13/h1-7H,8-12H2,(H,16,17,18)
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n/an/a 1.26E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM10404
PNG
((1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetrac...)
Show SMILES COc1ccc2CN(C)CC[C@@]34C=C[C@H](O)C[C@@H]3Oc1c24 |r,c:12|
Show InChI InChI=1S/C17H21NO3/c1-18-8-7-17-6-5-12(19)9-14(17)21-16-13(20-2)4-3-11(10-18)15(16)17/h3-6,12,14,19H,7-10H2,1-2H3/t12-,14-,17-/m0/s1
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n/an/a 1.26E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50319980
PNG
(CHEMBL1084212 | N-(naphthalen-1-ylmethyl)-2-thiomo...)
Show SMILES C(Nc1ccnc(n1)N1CCSCC1)c1cccc2ccccc12
Show InChI InChI=1S/C19H20N4S/c1-2-7-17-15(4-1)5-3-6-16(17)14-21-18-8-9-20-19(22-18)23-10-12-24-13-11-23/h1-9H,10-14H2,(H,20,21,22)
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n/an/a 1.28E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50319973
PNG
(CHEMBL1082978 | N-phenethyl-2-(pyrrolidin-1-yl)pyr...)
Show SMILES C(Cc1ccccc1)Nc1ccnc(n1)N1CCCC1
Show InChI InChI=1S/C16H20N4/c1-2-6-14(7-3-1)8-10-17-15-9-11-18-16(19-15)20-12-4-5-13-20/h1-3,6-7,9,11H,4-5,8,10,12-13H2,(H,17,18,19)
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n/an/a 1.38E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50319969
PNG
(CHEMBL1085781 | N-benzyl-2-morpholinopyrimidin-4-a...)
Show SMILES C(Nc1ccnc(n1)N1CCOCC1)c1ccccc1
Show InChI InChI=1S/C15H18N4O/c1-2-4-13(5-3-1)12-17-14-6-7-16-15(18-14)19-8-10-20-11-9-19/h1-7H,8-12H2,(H,16,17,18)
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n/an/a 1.40E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50342162
PNG
(CHEMBL1766020 | N-Benzyl-2-(4-isopropylpiperidin-1...)
Show SMILES CC(C)C1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C19H26N4/c1-15(2)17-9-12-23(13-10-17)19-20-11-8-18(22-19)21-14-16-6-4-3-5-7-16/h3-8,11,15,17H,9-10,12-14H2,1-2H3,(H,20,21,22)
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n/an/a 1.42E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50342157
PNG
(CHEMBL1766143 | N-Benzyl-2-[4-(4-bromobenzyl)piper...)
Show SMILES Brc1ccc(CN2CCN(CC2)c2nccc(NCc3ccccc3)n2)cc1
Show InChI InChI=1S/C22H24BrN5/c23-20-8-6-19(7-9-20)17-27-12-14-28(15-13-27)22-24-11-10-21(26-22)25-16-18-4-2-1-3-5-18/h1-11H,12-17H2,(H,24,25,26)
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n/an/a 1.43E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50319979
PNG
(2-morpholino-N-(naphthalen-1-ylmethyl)pyrimidin-4-...)
Show SMILES C(Nc1ccnc(n1)N1CCOCC1)c1cccc2ccccc12
Show InChI InChI=1S/C19H20N4O/c1-2-7-17-15(4-1)5-3-6-16(17)14-21-18-8-9-20-19(22-18)23-10-12-24-13-11-23/h1-9H,10-14H2,(H,20,21,22)
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n/an/a 1.47E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50342161
PNG
(CHEMBL1766139 | N-Benzyl-2-(4-propylpiperazin-1-yl...)
Show SMILES CCCN1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C18H25N5/c1-2-10-22-11-13-23(14-12-22)18-19-9-8-17(21-18)20-15-16-6-4-3-5-7-16/h3-9H,2,10-15H2,1H3,(H,19,20,21)
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n/an/a 1.53E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50342151
PNG
(CHEMBL1766149 | N-benzyl-2-(piperazin-1-yl)pyrimid...)
Show SMILES C(Nc1ccnc(n1)N1CCNCC1)c1ccccc1
Show InChI InChI=1S/C15H19N5/c1-2-4-13(5-3-1)12-18-14-6-7-17-15(19-14)20-10-8-16-9-11-20/h1-7,16H,8-12H2,(H,17,18,19)
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n/an/a 1.55E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50342147
PNG
(1-[4-(4-(Benzylamino)pyrimidin-2-yl)piperazin-1-yl...)
Show SMILES CC(=O)N1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C17H21N5O/c1-14(23)21-9-11-22(12-10-21)17-18-8-7-16(20-17)19-13-15-5-3-2-4-6-15/h2-8H,9-13H2,1H3,(H,18,19,20)
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n/an/a 1.66E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50319981
PNG
(2-(4-methylpiperazin-1-yl)-N-(naphthalen-1-ylmethy...)
Show SMILES CN1CCN(CC1)c1nccc(NCc2cccc3ccccc23)n1
Show InChI InChI=1S/C20H23N5/c1-24-11-13-25(14-12-24)20-21-10-9-19(23-20)22-15-17-7-4-6-16-5-2-3-8-18(16)17/h2-10H,11-15H2,1H3,(H,21,22,23)
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n/an/a 1.75E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50319977
PNG
(2-(4-methylpiperidin-1-yl)-N-phenethylpyrimidin-4-...)
Show SMILES CC1CCN(CC1)c1nccc(NCCc2ccccc2)n1
Show InChI InChI=1S/C18H24N4/c1-15-9-13-22(14-10-15)18-20-12-8-17(21-18)19-11-7-16-5-3-2-4-6-16/h2-6,8,12,15H,7,9-11,13-14H2,1H3,(H,19,20,21)
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n/an/a 1.77E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50319972
PNG
(CHEMBL1082977 | N-benzyl-2-(4-methylpiperidin-1-yl...)
Show SMILES CC1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C17H22N4/c1-14-8-11-21(12-9-14)17-18-10-7-16(20-17)19-13-15-5-3-2-4-6-15/h2-7,10,14H,8-9,11-13H2,1H3,(H,18,19,20)
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n/an/a 1.84E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50342146
PNG
(CHEMBL1766017 | tert-Butyl 4-[4-(Benzylamino)pyrim...)
Show SMILES CC(C)(C)OC(=O)N1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C20H27N5O2/c1-20(2,3)27-19(26)25-13-11-24(12-14-25)18-21-10-9-17(23-18)22-15-16-7-5-4-6-8-16/h4-10H,11-15H2,1-3H3,(H,21,22,23)
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n/an/a 1.88E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50319974
PNG
(2-morpholino-N-phenethylpyrimidin-4-amine | CHEMBL...)
Show SMILES C(Cc1ccccc1)Nc1ccnc(n1)N1CCOCC1
Show InChI InChI=1S/C16H20N4O/c1-2-4-14(5-3-1)6-8-17-15-7-9-18-16(19-15)20-10-12-21-13-11-20/h1-5,7,9H,6,8,10-13H2,(H,17,18,19)
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n/an/a 1.97E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50342150
PNG
(1-[4-(4-(Phenethylamino)pyrimidin-2-yl)piperazin-1...)
Show SMILES CC(=O)N1CCN(CC1)c1nccc(NCCc2ccccc2)n1
Show InChI InChI=1S/C18H23N5O/c1-15(24)22-11-13-23(14-12-22)18-20-10-8-17(21-18)19-9-7-16-5-3-2-4-6-16/h2-6,8,10H,7,9,11-14H2,1H3,(H,19,20,21)
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n/an/a 1.99E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50342158
PNG
(CHEMBL1766142 | N-Benzyl-2-[4-(4-chlorobenzyl)pipe...)
Show SMILES Clc1ccc(CN2CCN(CC2)c2nccc(NCc3ccccc3)n2)cc1
Show InChI InChI=1S/C22H24ClN5/c23-20-8-6-19(7-9-20)17-27-12-14-28(15-13-27)22-24-11-10-21(26-22)25-16-18-4-2-1-3-5-18/h1-11H,12-17H2,(H,24,25,26)
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n/an/a 2.02E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50319976
PNG
(2-(4-methylpiperazin-1-yl)-N-phenethylpyrimidin-4-...)
Show SMILES CN1CCN(CC1)c1nccc(NCCc2ccccc2)n1
Show InChI InChI=1S/C17H23N5/c1-21-11-13-22(14-12-21)17-19-10-8-16(20-17)18-9-7-15-5-3-2-4-6-15/h2-6,8,10H,7,9,11-14H2,1H3,(H,18,19,20)
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n/an/a 2.04E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50342156
PNG
(CHEMBL1766144 | N-Benzyl-2-[4-(4-fluorobenzyl)pipe...)
Show SMILES Fc1ccc(CN2CCN(CC2)c2nccc(NCc3ccccc3)n2)cc1
Show InChI InChI=1S/C22H24FN5/c23-20-8-6-19(7-9-20)17-27-12-14-28(15-13-27)22-24-11-10-21(26-22)25-16-18-4-2-1-3-5-18/h1-11H,12-17H2,(H,24,25,26)
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n/an/a 2.16E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50342145
PNG
(CHEMBL1766018 | N-Benzyl-2-(4-cyclohexylpiperazin-...)
Show SMILES C(Nc1ccnc(n1)N1CCN(CC1)C1CCCCC1)c1ccccc1
Show InChI InChI=1S/C21H29N5/c1-3-7-18(8-4-1)17-23-20-11-12-22-21(24-20)26-15-13-25(14-16-26)19-9-5-2-6-10-19/h1,3-4,7-8,11-12,19H,2,5-6,9-10,13-17H2,(H,22,23,24)
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n/an/a 2.29E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50319970
PNG
(CHEMBL1086014 | N-benzyl-2-thiomorpholinopyrimidin...)
Show SMILES C(Nc1ccnc(n1)N1CCSCC1)c1ccccc1
Show InChI InChI=1S/C15H18N4S/c1-2-4-13(5-3-1)12-17-14-6-7-16-15(18-14)19-8-10-20-11-9-19/h1-7H,8-12H2,(H,16,17,18)
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n/an/a 2.32E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50342152
PNG
(4-[4-(benzylamino)pyrimidin-2-yl]thiomorpholine-1,...)
Show SMILES O=S1(=O)CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C15H18N4O2S/c20-22(21)10-8-19(9-11-22)15-16-7-6-14(18-15)17-12-13-4-2-1-3-5-13/h1-7H,8-12H2,(H,16,17,18)
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n/an/a 2.42E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50319971
PNG
(CHEMBL1084808 | N-benzyl-2-(4-methylpiperazin-1-yl...)
Show SMILES CN1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C16H21N5/c1-20-9-11-21(12-10-20)16-17-8-7-15(19-16)18-13-14-5-3-2-4-6-14/h2-8H,9-13H2,1H3,(H,17,18,19)
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n/an/a 2.49E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50342163
PNG
(CHEMBL1766019 | N-Benzyl-2-(4-isopropylpiperazin-1...)
Show SMILES CC(C)N1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C18H25N5/c1-15(2)22-10-12-23(13-11-22)18-19-9-8-17(21-18)20-14-16-6-4-3-5-7-16/h3-9,15H,10-14H2,1-2H3,(H,19,20,21)
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n/an/a 2.50E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50342157
PNG
(CHEMBL1766143 | N-Benzyl-2-[4-(4-bromobenzyl)piper...)
Show SMILES Brc1ccc(CN2CCN(CC2)c2nccc(NCc3ccccc3)n2)cc1
Show InChI InChI=1S/C22H24BrN5/c23-20-8-6-19(7-9-20)17-27-12-14-28(15-13-27)22-24-11-10-21(26-22)25-16-18-4-2-1-3-5-18/h1-11H,12-17H2,(H,24,25,26)
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n/an/a 2.55E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50342149
PNG
(2-(4-Methylpiperidin-1-yl)-N-(naphth-1-ylmethyl)py...)
Show SMILES CC1CCN(CC1)c1nccc(NCc2cccc3ccccc23)n1
Show InChI InChI=1S/C21H24N4/c1-16-10-13-25(14-11-16)21-22-12-9-20(24-21)23-15-18-7-4-6-17-5-2-3-8-19(17)18/h2-9,12,16H,10-11,13-15H2,1H3,(H,22,23,24)
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n/an/a 2.58E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50319975
PNG
(CHEMBL1082979 | N-phenethyl-2-thiomorpholinopyrimi...)
Show SMILES C(Cc1ccccc1)Nc1ccnc(n1)N1CCSCC1
Show InChI InChI=1S/C16H20N4S/c1-2-4-14(5-3-1)6-8-17-15-7-9-18-16(19-15)20-10-12-21-13-11-20/h1-5,7,9H,6,8,10-13H2,(H,17,18,19)
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n/an/a 2.64E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50319968
PNG
(CHEMBL1085780 | N-benzyl-2-(pyrrolidin-1-yl)pyrimi...)
Show SMILES C(Nc1ccnc(n1)N1CCCC1)c1ccccc1
Show InChI InChI=1S/C15H18N4/c1-2-6-13(7-3-1)12-17-14-8-9-16-15(18-14)19-10-4-5-11-19/h1-3,6-9H,4-5,10-12H2,(H,16,17,18)
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n/an/a 2.64E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50342160
PNG
(2-[4-(4-(Benzylamino)pyrimidin-2-yl)piperazin-1-yl...)
Show SMILES OCCN1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C17H23N5O/c23-13-12-21-8-10-22(11-9-21)17-18-7-6-16(20-17)19-14-15-4-2-1-3-5-15/h1-7,23H,8-14H2,(H,18,19,20)
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n/an/a 2.64E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50342159
PNG
(CHEMBL1766141 | N-Benzyl-2-[4-(2-methoxyethyl)pipe...)
Show SMILES COCCN1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C18H25N5O/c1-24-14-13-22-9-11-23(12-10-22)18-19-8-7-17(21-18)20-15-16-5-3-2-4-6-16/h2-8H,9-15H2,1H3,(H,19,20,21)
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n/an/a 2.67E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50319979
PNG
(2-morpholino-N-(naphthalen-1-ylmethyl)pyrimidin-4-...)
Show SMILES C(Nc1ccnc(n1)N1CCOCC1)c1cccc2ccccc12
Show InChI InChI=1S/C19H20N4O/c1-2-7-17-15(4-1)5-3-6-16(17)14-21-18-8-9-20-19(22-18)23-10-12-24-13-11-23/h1-9H,10-14H2,(H,20,21,22)
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n/an/a 2.80E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50342155
PNG
(CHEMBL1766145 | N-Benzyl-2-[4-(4-trifluoromethylbe...)
Show SMILES FC(F)(F)c1ccc(CN2CCN(CC2)c2nccc(NCc3ccccc3)n2)cc1
Show InChI InChI=1S/C23H24F3N5/c24-23(25,26)20-8-6-19(7-9-20)17-30-12-14-31(15-13-30)22-27-11-10-21(29-22)28-16-18-4-2-1-3-5-18/h1-11H,12-17H2,(H,27,28,29)
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n/an/a 2.88E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50319980
PNG
(CHEMBL1084212 | N-(naphthalen-1-ylmethyl)-2-thiomo...)
Show SMILES C(Nc1ccnc(n1)N1CCSCC1)c1cccc2ccccc12
Show InChI InChI=1S/C19H20N4S/c1-2-7-17-15(4-1)5-3-6-16(17)14-21-18-8-9-20-19(22-18)23-10-12-24-13-11-23/h1-9H,10-14H2,(H,20,21,22)
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n/an/a 3.47E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50342161
PNG
(CHEMBL1766139 | N-Benzyl-2-(4-propylpiperazin-1-yl...)
Show SMILES CCCN1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C18H25N5/c1-2-10-22-11-13-23(14-12-22)18-19-9-8-17(21-18)20-15-16-6-4-3-5-7-16/h3-9H,2,10-15H2,1H3,(H,19,20,21)
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n/an/a 5.99E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50319969
PNG
(CHEMBL1085781 | N-benzyl-2-morpholinopyrimidin-4-a...)
Show SMILES C(Nc1ccnc(n1)N1CCOCC1)c1ccccc1
Show InChI InChI=1S/C15H18N4O/c1-2-4-13(5-3-1)12-17-14-6-7-16-15(18-14)19-8-10-20-11-9-19/h1-7H,8-12H2,(H,16,17,18)
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n/an/a 6.83E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50319975
PNG
(CHEMBL1082979 | N-phenethyl-2-thiomorpholinopyrimi...)
Show SMILES C(Cc1ccccc1)Nc1ccnc(n1)N1CCSCC1
Show InChI InChI=1S/C16H20N4S/c1-2-4-14(5-3-1)6-8-17-15-7-9-18-16(19-15)20-10-12-21-13-11-20/h1-5,7,9H,6,8,10-13H2,(H,17,18,19)
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n/an/a>1.00E+5n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50319976
PNG
(2-(4-methylpiperazin-1-yl)-N-phenethylpyrimidin-4-...)
Show SMILES CN1CCN(CC1)c1nccc(NCCc2ccccc2)n1
Show InChI InChI=1S/C17H23N5/c1-21-11-13-22(14-12-21)17-19-10-8-16(20-17)18-9-7-15-5-3-2-4-6-15/h2-6,8,10H,7,9,11-14H2,1H3,(H,18,19,20)
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n/an/a>1.00E+5n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50342150
PNG
(1-[4-(4-(Phenethylamino)pyrimidin-2-yl)piperazin-1...)
Show SMILES CC(=O)N1CCN(CC1)c1nccc(NCCc2ccccc2)n1
Show InChI InChI=1S/C18H23N5O/c1-15(24)22-11-13-23(14-12-22)18-20-10-8-17(21-18)19-9-7-16-5-3-2-4-6-16/h2-6,8,10H,7,9,11-14H2,1H3,(H,19,20,21)
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n/an/a>1.00E+5n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50342159
PNG
(CHEMBL1766141 | N-Benzyl-2-[4-(2-methoxyethyl)pipe...)
Show SMILES COCCN1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C18H25N5O/c1-24-14-13-22-9-11-23(12-10-22)18-19-8-7-17(21-18)20-15-16-5-3-2-4-6-16/h2-8H,9-15H2,1H3,(H,19,20,21)
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n/an/a>1.00E+5n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50342151
PNG
(CHEMBL1766149 | N-benzyl-2-(piperazin-1-yl)pyrimid...)
Show SMILES C(Nc1ccnc(n1)N1CCNCC1)c1ccccc1
Show InChI InChI=1S/C15H19N5/c1-2-4-13(5-3-1)12-18-14-6-7-17-15(19-14)20-10-8-16-9-11-20/h1-7,16H,8-12H2,(H,17,18,19)
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n/an/a>1.00E+5n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50319974
PNG
(2-morpholino-N-phenethylpyrimidin-4-amine | CHEMBL...)
Show SMILES C(Cc1ccccc1)Nc1ccnc(n1)N1CCOCC1
Show InChI InChI=1S/C16H20N4O/c1-2-4-14(5-3-1)6-8-17-15-7-9-18-16(19-15)20-10-12-21-13-11-20/h1-5,7,9H,6,8,10-13H2,(H,17,18,19)
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n/an/a>1.00E+5n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50342155
PNG
(CHEMBL1766145 | N-Benzyl-2-[4-(4-trifluoromethylbe...)
Show SMILES FC(F)(F)c1ccc(CN2CCN(CC2)c2nccc(NCc3ccccc3)n2)cc1
Show InChI InChI=1S/C23H24F3N5/c24-23(25,26)20-8-6-19(7-9-20)17-30-12-14-31(15-13-30)22-27-11-10-21(29-22)28-16-18-4-2-1-3-5-18/h1-11H,12-17H2,(H,27,28,29)
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n/an/a>1.00E+5n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50342146
PNG
(CHEMBL1766017 | tert-Butyl 4-[4-(Benzylamino)pyrim...)
Show SMILES CC(C)(C)OC(=O)N1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C20H27N5O2/c1-20(2,3)27-19(26)25-13-11-24(12-14-25)18-21-10-9-17(23-18)22-15-16-7-5-4-6-8-16/h4-10H,11-15H2,1-3H3,(H,21,22,23)
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n/an/a>1.00E+5n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50319971
PNG
(CHEMBL1084808 | N-benzyl-2-(4-methylpiperazin-1-yl...)
Show SMILES CN1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C16H21N5/c1-20-9-11-21(12-10-20)16-17-8-7-15(19-16)18-13-14-5-3-2-4-6-14/h2-8H,9-13H2,1H3,(H,17,18,19)
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n/an/a>1.00E+5n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50342160
PNG
(2-[4-(4-(Benzylamino)pyrimidin-2-yl)piperazin-1-yl...)
Show SMILES OCCN1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C17H23N5O/c23-13-12-21-8-10-22(11-9-21)17-18-7-6-16(20-17)19-14-15-4-2-1-3-5-15/h1-7,23H,8-14H2,(H,18,19,20)
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n/an/a>1.00E+5n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50342147
PNG
(1-[4-(4-(Benzylamino)pyrimidin-2-yl)piperazin-1-yl...)
Show SMILES CC(=O)N1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C17H21N5O/c1-14(23)21-9-11-22(12-10-21)17-18-8-7-16(20-17)19-13-15-5-3-2-4-6-15/h2-8H,9-13H2,1H3,(H,18,19,20)
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n/an/a>1.00E+5n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50342153
PNG
(4-[4-(benzylamino)pyrimidin-2-yl]thiomorpholine-1-...)
Show SMILES O=S1CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C15H18N4OS/c20-21-10-8-19(9-11-21)15-16-7-6-14(18-15)17-12-13-4-2-1-3-5-13/h1-7H,8-12H2,(H,16,17,18)
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n/an/a>1.00E+5n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50342152
PNG
(4-[4-(benzylamino)pyrimidin-2-yl]thiomorpholine-1,...)
Show SMILES O=S1(=O)CCN(CC1)c1nccc(NCc2ccccc2)n1
Show InChI InChI=1S/C15H18N4O2S/c20-22(21)10-8-19(9-11-22)15-16-7-6-14(18-15)17-12-13-4-2-1-3-5-13/h1-7H,8-12H2,(H,16,17,18)
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n/an/a>1.00E+5n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem 19: 2269-81 (2011)


Article DOI: 10.1016/j.bmc.2011.02.030
BindingDB Entry DOI: 10.7270/Q2Q240JH
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%