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Compile Data Set for Download or QSAR

Found 41 hits with Last Name = 'mostofi' and Initial = 'm'   
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
Cholinesterase


(Equus caballus (Horse))		BDBM50275270
PNG
(CHEMBL4126207)
Show SMILES COc1cccc(c1)C1CC(=Nc2ccccc2S1)c1cc2cc(Br)ccc2o1 |c:11|
Show InChI InChI=1S/C24H18BrNO2S/c1-27-18-6-4-5-15(12-18)24-14-20(26-19-7-2-3-8-23(19)29-24)22-13-16-11-17(25)9-10-21(16)28-22/h2-13,24H,14H2,1H3
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 100n/an/an/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Mixed-type inhibition of equine serum BChE using varying levels of butyrylthiocholine iodide as substrate pretreated for 10 mins followed by substrat...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		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 23n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair		3D
3D Structure (crystal)
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		BDBM50131762
PNG
(CHEMBL3633865)
Show SMILES [Br-].COc1cccc2cc(oc12)C(=O)\C=C\c1ccc[n+](Cc2ccccc2Br)c1
Show InChI InChI=1S/C24H19BrNO3.BrH/c1-28-22-10-4-8-18-14-23(29-24(18)22)21(27)12-11-17-6-5-13-26(15-17)16-19-7-2-3-9-20(19)25;/h2-15H,16H2,1H3;1H/q+1;/p-1/b12-11+;
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n/an/a 27n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		BDBM50131771
PNG
(CHEMBL3633525)
Show SMILES [Br-].Brc1ccccc1C[n+]1cccc(\C=C\C(=O)c2cc3ccccc3o2)c1
Show InChI InChI=1S/C23H17BrNO2.BrH/c24-20-9-3-1-8-19(20)16-25-13-5-6-17(15-25)11-12-21(26)23-14-18-7-2-4-10-22(18)27-23;/h1-15H,16H2;1H/q+1;/p-1/b12-11+;
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n/an/a 35n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		BDBM50131718
PNG
(CHEMBL3633870)
Show SMILES [Br-].Brc1ccccc1C[n+]1ccc(\C=C\C(=O)c2cc3ccccc3o2)cc1
Show InChI InChI=1S/C23H17BrNO2.BrH/c24-20-7-3-1-6-19(20)16-25-13-11-17(12-14-25)9-10-21(26)23-15-18-5-2-4-8-22(18)27-23;/h1-15H,16H2;1H/q+1;/p-1/b10-9+;
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n/an/a 41n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		BDBM50131772
PNG
(CHEMBL3633524)
Show SMILES [Br-].O=C(\C=C\c1ccc[n+](Cc2ccccc2)c1)c1cc2ccccc2o1
Show InChI InChI=1S/C23H18NO2.BrH/c25-21(23-15-20-10-4-5-11-22(20)26-23)13-12-19-9-6-14-24(17-19)16-18-7-2-1-3-8-18;/h1-15,17H,16H2;1H/q+1;/p-1/b13-12+;
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n/an/a 58n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		BDBM50131758
PNG
(CHEMBL3633869)
Show SMILES [Br-].O=C(\C=C\c1cc[n+](Cc2ccccc2)cc1)c1cc2ccccc2o1
Show InChI InChI=1S/C23H18NO2.BrH/c25-21(23-16-20-8-4-5-9-22(20)26-23)11-10-18-12-14-24(15-13-18)17-19-6-2-1-3-7-19;/h1-16H,17H2;1H/q+1;/p-1/b11-10+;
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n/an/a 64n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		BDBM50131770
PNG
(CHEMBL3633857)
Show SMILES [Br-].Brc1ccc(C[n+]2cccc(\C=C\C(=O)c3cc4ccccc4o3)c2)cc1
Show InChI InChI=1S/C23H17BrNO2.BrH/c24-20-10-7-18(8-11-20)16-25-13-3-4-17(15-25)9-12-21(26)23-14-19-5-1-2-6-22(19)27-23;/h1-15H,16H2;1H/q+1;/p-1/b12-9+;
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n/an/a 357n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		BDBM50131764
PNG
(CHEMBL3633863)
Show SMILES [Cl-].Clc1ccc(C[n+]2cccc(\C=C\C(=O)c3cc4cc(Br)ccc4o3)c2)cc1Cl
Show InChI InChI=1S/C23H15BrCl2NO2.ClH/c24-18-5-8-22-17(11-18)12-23(29-22)21(28)7-4-15-2-1-9-27(13-15)14-16-3-6-19(25)20(26)10-16;/h1-13H,14H2;1H/q+1;/p-1/b7-4+;
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n/an/a 786n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		BDBM50131759
PNG
(CHEMBL3633868)
Show SMILES [Cl-].COc1cccc2cc(oc12)C(=O)\C=C\c1ccc[n+](Cc2cccc(Cl)c2Cl)c1
Show InChI InChI=1S/C24H18Cl2NO3.ClH/c1-29-21-9-3-6-17-13-22(30-24(17)21)20(28)11-10-16-5-4-12-27(14-16)15-18-7-2-8-19(25)23(18)26;/h2-14H,15H2,1H3;1H/q+1;/p-1/b11-10+;
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n/an/a 985n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275270
PNG
(CHEMBL4126207)
Show SMILES COc1cccc(c1)C1CC(=Nc2ccccc2S1)c1cc2cc(Br)ccc2o1 |c:11|
Show InChI InChI=1S/C24H18BrNO2S/c1-27-18-6-4-5-15(12-18)24-14-20(26-19-7-2-3-8-23(19)29-24)22-13-16-11-17(25)9-10-21(16)28-22/h2-13,24H,14H2,1H3
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n/an/a 1.00E+3n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275230
PNG
(CHEMBL4126049)
Show SMILES COc1ccc(cc1)C1CC(=Nc2ccccc2S1)c1cc2cc(Br)ccc2o1 |c:11|
Show InChI InChI=1S/C24H18BrNO2S/c1-27-18-9-6-15(7-10-18)24-14-20(26-19-4-2-3-5-23(19)29-24)22-13-16-12-17(25)8-11-21(16)28-22/h2-13,24H,14H2,1H3
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n/an/a 1.00E+3n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275269
PNG
(CHEMBL4129504)
Show SMILES COc1ccccc1C1CC(=Nc2ccccc2S1)c1cc2cc(Br)ccc2o1 |c:11|
Show InChI InChI=1S/C24H18BrNO2S/c1-27-21-8-4-2-6-17(21)24-14-19(26-18-7-3-5-9-23(18)29-24)22-13-15-12-16(25)10-11-20(15)28-22/h2-13,24H,14H2,1H3
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n/an/a 1.80E+3n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		BDBM50131767
PNG
(CHEMBL3633860)
Show SMILES [Br-].Brc1ccc2oc(cc2c1)C(=O)\C=C\c1ccc[n+](Cc2ccccc2Br)c1
Show InChI InChI=1S/C23H16Br2NO2.BrH/c24-19-8-10-22-18(12-19)13-23(28-22)21(27)9-7-16-4-3-11-26(14-16)15-17-5-1-2-6-20(17)25;/h1-14H,15H2;1H/q+1;/p-1/b9-7+;
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n/an/a 2.15E+3n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275253
PNG
(CHEMBL4130033)
Show SMILES COc1cccc2cc(oc12)C1=Nc2ccccc2SC(C1)c1ccccc1 |t:13|
Show InChI InChI=1S/C24H19NO2S/c1-26-20-12-7-10-17-14-21(27-24(17)20)19-15-23(16-8-3-2-4-9-16)28-22-13-6-5-11-18(22)25-19/h2-14,23H,15H2,1H3
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n/an/a 2.50E+3n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Cholinesterase


(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 2.63E+3n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		BDBM50131765
PNG
(CHEMBL3633862)
Show SMILES [Cl-].Clc1cccc(C[n+]2cccc(\C=C\C(=O)c3cc4cc(Br)ccc4o3)c2)c1Cl
Show InChI InChI=1S/C23H15BrCl2NO2.ClH/c24-18-7-9-21-17(11-18)12-22(29-21)20(28)8-6-15-3-2-10-27(13-15)14-16-4-1-5-19(25)23(16)26;/h1-13H,14H2;1H/q+1;/p-1/b8-6+;
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n/an/a 2.85E+3n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		BDBM50131717
PNG
(CHEMBL3633871)
Show SMILES [Cl-].Clc1cccc(C[n+]2ccc(\C=C\C(=O)c3cc4ccccc4o3)cc2)c1Cl
Show InChI InChI=1S/C23H16Cl2NO2.ClH/c24-19-6-3-5-18(23(19)25)15-26-12-10-16(11-13-26)8-9-20(27)22-14-17-4-1-2-7-21(17)28-22;/h1-14H,15H2;1H/q+1;/p-1/b9-8+;
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n/an/a 3.12E+3n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		BDBM50131763
PNG
(CHEMBL3633864)
Show SMILES [Br-].COc1cccc2cc(oc12)C(=O)\C=C\c1ccc[n+](Cc2ccccc2)c1
Show InChI InChI=1S/C24H20NO3.BrH/c1-27-22-11-5-10-20-15-23(28-24(20)22)21(26)13-12-19-9-6-14-25(17-19)16-18-7-3-2-4-8-18;/h2-15,17H,16H2,1H3;1H/q+1;/p-1/b13-12+;
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n/an/a 3.89E+3n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275245
PNG
(CHEMBL4126460)
Show SMILES COc1ccc(cc1)C1CC(=Nc2ccccc2S1)c1cc2ccccc2o1 |c:11|
Show InChI InChI=1S/C24H19NO2S/c1-26-18-12-10-16(11-13-18)24-15-20(25-19-7-3-5-9-23(19)28-24)22-14-17-6-2-4-8-21(17)27-22/h2-14,24H,15H2,1H3
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n/an/a 4.00E+3n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275244
PNG
(CHEMBL4127850)
Show SMILES COc1cccc(c1)C1CC(=Nc2ccccc2S1)c1cc2ccccc2o1 |c:11|
Show InChI InChI=1S/C24H19NO2S/c1-26-18-9-6-8-17(13-18)24-15-20(25-19-10-3-5-12-23(19)28-24)22-14-16-7-2-4-11-21(16)27-22/h2-14,24H,15H2,1H3
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n/an/a 4.10E+3n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275254
PNG
(CHEMBL4128663)
Show SMILES COc1cccc2cc(oc12)C1=Nc2ccccc2SC(C1)c1ccc(O)cc1 |t:13|
Show InChI InChI=1S/C24H19NO3S/c1-27-20-7-4-5-16-13-21(28-24(16)20)19-14-23(15-9-11-17(26)12-10-15)29-22-8-3-2-6-18(22)25-19/h2-13,23,26H,14H2,1H3
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n/an/a 4.10E+3n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275238
PNG
(CHEMBL4130145)
Show SMILES COc1ccccc1C1CC(=Nc2ccccc2S1)c1cc2ccccc2o1 |c:11|
Show InChI InChI=1S/C24H19NO2S/c1-26-21-12-6-3-9-17(21)24-15-19(25-18-10-4-7-13-23(18)28-24)22-14-16-8-2-5-11-20(16)27-22/h2-14,24H,15H2,1H3
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n/an/a 4.80E+3n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		BDBM50131768
PNG
(CHEMBL3633859)
Show SMILES [Br-].Brc1ccc2oc(cc2c1)C(=O)\C=C\c1ccc[n+](Cc2ccccc2)c1
Show InChI InChI=1S/C23H17BrNO2.BrH/c24-20-9-11-22-19(13-20)14-23(27-22)21(26)10-8-18-7-4-12-25(16-18)15-17-5-2-1-3-6-17;/h1-14,16H,15H2;1H/q+1;/p-1/b10-8+;
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n/an/a 5.41E+3n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		BDBM50131715
PNG
(CHEMBL3633872)
Show SMILES [Br-].Brc1ccc2oc(cc2c1)C(=O)\C=C\c1cc[n+](Cc2ccccc2)cc1
Show InChI InChI=1S/C23H17BrNO2.BrH/c24-20-7-9-22-19(14-20)15-23(27-22)21(26)8-6-17-10-12-25(13-11-17)16-18-4-2-1-3-5-18;/h1-15H,16H2;1H/q+1;/p-1/b8-6+;
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n/an/a 5.96E+3n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275268
PNG
(CHEMBL4129645)
Show SMILES Oc1ccc(cc1)C1CC(=Nc2ccccc2S1)c1cc2cc(Br)ccc2o1 |c:10|
Show InChI InChI=1S/C23H16BrNO2S/c24-16-7-10-20-15(11-16)12-21(27-20)19-13-23(14-5-8-17(26)9-6-14)28-22-4-2-1-3-18(22)25-19/h1-12,23,26H,13H2
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n/an/a 6.50E+3n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275255
PNG
(CHEMBL4128273)
Show SMILES Brc1ccc2oc(cc2c1)C1=Nc2ccccc2SC(C1)c1ccccc1 |t:12|
Show InChI InChI=1S/C23H16BrNOS/c24-17-10-11-20-16(12-17)13-21(26-20)19-14-23(15-6-2-1-3-7-15)27-22-9-5-4-8-18(22)25-19/h1-13,23H,14H2
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n/an/a 8.50E+3n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275271
PNG
(CHEMBL4127431)
Show SMILES Cc1ccc(cc1)C1CC(=Nc2ccccc2S1)c1cc2cc(Br)ccc2o1 |c:10|
Show InChI InChI=1S/C24H18BrNOS/c1-15-6-8-16(9-7-15)24-14-20(26-19-4-2-3-5-23(19)28-24)22-13-17-12-18(25)10-11-21(17)27-22/h2-13,24H,14H2,1H3
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n/an/a 8.50E+3n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		BDBM50131761
PNG
(CHEMBL3633866)
Show SMILES [Br-].COc1cccc2cc(oc12)C(=O)\C=C\c1ccc[n+](Cc2ccc(Br)cc2)c1
Show InChI InChI=1S/C24H19BrNO3.BrH/c1-28-22-6-2-5-19-14-23(29-24(19)22)21(27)12-9-17-4-3-13-26(15-17)16-18-7-10-20(25)11-8-18;/h2-15H,16H2,1H3;1H/q+1;/p-1/b12-9+;
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n/an/a 1.07E+4n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		BDBM50131760
PNG
(CHEMBL3633867)
Show SMILES [Cl-].COc1cccc2cc(oc12)C(=O)\C=C\c1ccc[n+](Cc2ccc(Cl)cc2)c1
Show InChI InChI=1S/C24H19ClNO3.ClH/c1-28-22-6-2-5-19-14-23(29-24(19)22)21(27)12-9-17-4-3-13-26(15-17)16-18-7-10-20(25)11-8-18;/h2-15H,16H2,1H3;1H/q+1;/p-1/b12-9+;
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n/an/a 1.12E+4n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275272
PNG
(CHEMBL4127288)
Show SMILES Fc1ccccc1C1CC(=Nc2ccccc2S1)c1cc2cc(Br)ccc2o1 |c:10|
Show InChI InChI=1S/C23H15BrFNOS/c24-15-9-10-20-14(11-15)12-21(27-20)19-13-23(16-5-1-2-6-17(16)25)28-22-8-4-3-7-18(22)26-19/h1-12,23H,13H2
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n/an/a 1.37E+4n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275237
PNG
(CHEMBL4126881)
Show SMILES Oc1ccc(cc1)C1CC(=Nc2ccccc2S1)c1cc2ccccc2o1 |c:10|
Show InChI InChI=1S/C23H17NO2S/c25-17-11-9-15(10-12-17)23-14-19(24-18-6-2-4-8-22(18)27-23)21-13-16-5-1-3-7-20(16)26-21/h1-13,23,25H,14H2
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n/an/a 1.40E+4n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275309
PNG
(CHEMBL4128803)
Show SMILES Brc1ccc2oc(cc2c1)C1=Nc2ccccc2SC(C1)c1cccc2ccccc12 |t:12|
Show InChI InChI=1S/C27H18BrNOS/c28-19-12-13-24-18(14-19)15-25(30-24)23-16-27(31-26-11-4-3-10-22(26)29-23)21-9-5-7-17-6-1-2-8-20(17)21/h1-15,27H,16H2
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n/an/a 1.70E+4n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275310
PNG
(CHEMBL4129157)
Show SMILES [O-][N+](=O)c1ccc2oc(cc2c1)C1=Nc2ccccc2SC(C1)c1ccccc1F |t:14|
Show InChI InChI=1S/C23H15FN2O3S/c24-17-6-2-1-5-16(17)23-13-19(25-18-7-3-4-8-22(18)30-23)21-12-14-11-15(26(27)28)9-10-20(14)29-21/h1-12,23H,13H2
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n/an/a 2.20E+4n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275231
PNG
(CHEMBL4127739)
Show SMILES Brc1ccc2oc(cc2c1)C1=Nc2ccccc2SC(C1)c1c[nH]c2ccccc12 |t:12|
Show InChI InChI=1S/C25H17BrN2OS/c26-16-9-10-22-15(11-16)12-23(29-22)21-13-25(30-24-8-4-3-7-20(24)28-21)18-14-27-19-6-2-1-5-17(18)19/h1-12,14,25,27H,13H2
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n/an/a 2.80E+4n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		BDBM50131769
PNG
(CHEMBL3633858)
Show SMILES [Br-].[O-][N+](=O)c1ccc(C[n+]2cccc(\C=C\C(=O)c3cc4ccccc4o3)c2)cc1
Show InChI InChI=1S/C23H17N2O4.BrH/c26-21(23-14-19-5-1-2-6-22(19)29-23)12-9-17-4-3-13-24(15-17)16-18-7-10-20(11-8-18)25(27)28;/h1-15H,16H2;1H/q+1;/p-1/b12-9+;
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n/an/a 2.92E+4n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Tetronarce californica (Pacific electric ray) (Tor...)		BDBM50131766
PNG
(CHEMBL3633861)
Show SMILES [Br-].Brc1ccc(C[n+]2cccc(\C=C\C(=O)c3cc4cc(Br)ccc4o3)c2)cc1
Show InChI InChI=1S/C23H16Br2NO2.BrH/c24-19-6-3-17(4-7-19)15-26-11-1-2-16(14-26)5-9-21(27)23-13-18-12-20(25)8-10-22(18)28-23;/h1-14H,15H2;1H/q+1;/p-1/b9-5+;
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n/an/a 3.10E+4n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of Torpedo californica AChE (type VI-S) using acetylthiocholine iodide as substrate assessed as 5-thio-2-nitrobenzoate anion formation pre...

Eur J Med Chem 103: 361-9 (2015)


Article DOI: 10.1016/j.ejmech.2015.08.061
BindingDB Entry DOI: 10.7270/Q2XK8HC1
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275311
PNG
(CHEMBL4129309)
Show SMILES [O-][N+](=O)c1ccc2oc(cc2c1)C1=Nc2ccccc2SC(C1)c1cccc2ccccc12 |t:14|
Show InChI InChI=1S/C27H18N2O3S/c30-29(31)19-12-13-24-18(14-19)15-25(32-24)23-16-27(33-26-11-4-3-10-22(26)28-23)21-9-5-7-17-6-1-2-8-20(17)21/h1-15,27H,16H2
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n/an/a 5.50E+4n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275247
PNG
(CHEMBL4127693)
Show SMILES C1C(Sc2ccccc2N=C1c1cc2ccccc2o1)c1c[nH]c2ccccc12 |c:10|
Show InChI InChI=1S/C25H18N2OS/c1-5-11-22-16(7-1)13-23(28-22)21-14-25(29-24-12-6-4-10-20(24)27-21)18-15-26-19-9-3-2-8-17(18)19/h1-13,15,25-26H,14H2
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n/an/a 6.00E+4n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275246
PNG
(CHEMBL4129086)
Show SMILES C1C(Sc2ccccc2N=C1c1cc2ccccc2o1)c1cccc2ccccc12 |c:10|
Show InChI InChI=1S/C27H19NOS/c1-3-11-20-18(8-1)10-7-12-21(20)27-17-23(28-22-13-4-6-15-26(22)30-27)25-16-19-9-2-5-14-24(19)29-25/h1-16,27H,17H2
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 6.30E+4n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50275236
PNG
(CHEMBL4127914)
Show SMILES [O-][N+](=O)c1ccc2oc(cc2c1)C1=Nc2ccccc2SC(C1)c1c[nH]c2ccccc12 |t:14|
Show InChI InChI=1S/C25H17N3O3S/c29-28(30)16-9-10-22-15(11-16)12-23(31-22)21-13-25(32-24-8-4-3-7-20(24)27-21)18-14-26-19-6-2-1-5-17(18)19/h1-12,14,25-26H,13H2
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 7.20E+4n/an/an/an/an/an/a



Alzahra University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate pretreated for 15 mins followed by substrate addition measured for 6 min...

Bioorg Med Chem 26: 3076-3095 (2018)


Article DOI: 10.1016/j.bmc.2018.02.049
BindingDB Entry DOI: 10.7270/Q2SF2ZPJ
More data for this
Ligand-Target Pair