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PubMed code 22001085

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
Liver carboxylesterase


(Sus scrofa)		BDBM50358312
PNG
(CHEMBL1922541)
Show SMILES COC(=O)C(OP(C)(=O)OCC#C)C(F)(F)F
Show InChI InChI=1S/C8H10F3O5P/c1-4-5-15-17(3,13)16-6(7(12)14-2)8(9,10)11/h1,6H,5H2,2-3H3
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n/an/a 6.06E+3n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of pig liver carboxylesterase using p-nitrophenyl acetate as substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Liver carboxylesterase


(Sus scrofa)		BDBM50358311
PNG
(CHEMBL1922540)
Show SMILES CP(=O)(OCC#C)OC(C(F)(F)F)C(F)(F)F
Show InChI InChI=1S/C7H7F6O3P/c1-3-4-15-17(2,14)16-5(6(8,9)10)7(11,12)13/h1,5H,4H2,2H3
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n/an/a 2.31E+4n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of pig liver carboxylesterase using p-nitrophenyl acetate as substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50358312
PNG
(CHEMBL1922541)
Show SMILES COC(=O)C(OP(C)(=O)OCC#C)C(F)(F)F
Show InChI InChI=1S/C8H10F3O5P/c1-4-5-15-17(3,13)16-6(7(12)14-2)8(9,10)11/h1,6H,5H2,2-3H3
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n/an/a 2.89E+4n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of horse serum BChE incubated for 12 mins before addition of butyrylcholine iodide substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))		BDBM50358312
PNG
(CHEMBL1922541)
Show SMILES COC(=O)C(OP(C)(=O)OCC#C)C(F)(F)F
Show InChI InChI=1S/C8H10F3O5P/c1-4-5-15-17(3,13)16-6(7(12)14-2)8(9,10)11/h1,6H,5H2,2-3H3
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n/an/a 4.36E+4n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocyte AChE incubated for 12 mins before addition of acetylthiocholine iodide substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Liver carboxylesterase


(Sus scrofa)		BDBM50358315
PNG
(CHEMBL1922544)
Show SMILES CC[C@H](C)[C@@H](Cn1cc(COP(C)(=O)OC(C(F)(F)F)C(F)(F)F)nn1)NC(=O)CN(Cc1ccccc1)C(=O)C(F)(F)F |r|
Show InChI InChI=1S/C24H29F9N5O5P/c1-4-15(2)18(34-19(39)13-37(21(40)24(31,32)33)10-16-8-6-5-7-9-16)12-38-11-17(35-36-38)14-42-44(3,41)43-20(22(25,26)27)23(28,29)30/h5-9,11,15,18,20H,4,10,12-14H2,1-3H3,(H,34,39)/t15-,18+,44?/m0/s1
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n/an/a 6.39E+4n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of pig liver carboxylesterase using p-nitrophenyl acetate as substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))		BDBM50358311
PNG
(CHEMBL1922540)
Show SMILES CP(=O)(OCC#C)OC(C(F)(F)F)C(F)(F)F
Show InChI InChI=1S/C7H7F6O3P/c1-3-4-15-17(2,14)16-5(6(8,9)10)7(11,12)13/h1,5H,4H2,2H3
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n/an/a 6.50E+4n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocyte AChE incubated for 12 mins before addition of acetylthiocholine iodide substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Liver carboxylesterase


(Sus scrofa)		BDBM50358320
PNG
(CHEMBL1922549)
Show SMILES COC(=O)C(OP(C)(=O)OCc1cn(C[C@@H](NC(=O)CN(Cc2ccccc2)C(=O)[C@H](C)NC(=O)OC(C)(C)C)C(C)C)nn1)C(F)(F)F |r|
Show InChI InChI=1S/C30H44F3N6O9P/c1-19(2)23(16-39-15-22(36-37-39)18-46-49(8,44)48-25(27(42)45-7)30(31,32)33)35-24(40)17-38(14-21-12-10-9-11-13-21)26(41)20(3)34-28(43)47-29(4,5)6/h9-13,15,19-20,23,25H,14,16-18H2,1-8H3,(H,34,43)(H,35,40)/t20-,23+,25?,49?/m0/s1
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n/an/a 7.93E+4n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of pig liver carboxylesterase using p-nitrophenyl acetate as substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Liver carboxylesterase


(Sus scrofa)		BDBM50358318
PNG
(CHEMBL1922547)
Show SMILES CC(C)[C@@H](Cn1cc(COP(C)(=O)OC(C(F)(F)F)C(F)(F)F)nn1)NC(=O)CN(Cc1ccccc1)C(=O)C(F)(F)F |r|
Show InChI InChI=1S/C23H27F9N5O5P/c1-14(2)17(33-18(38)12-36(20(39)23(30,31)32)9-15-7-5-4-6-8-15)11-37-10-16(34-35-37)13-41-43(3,40)42-19(21(24,25)26)22(27,28)29/h4-8,10,14,17,19H,9,11-13H2,1-3H3,(H,33,38)/t17-,43?/m1/s1
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n/an/a 8.58E+4n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of pig liver carboxylesterase using p-nitrophenyl acetate as substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Liver carboxylesterase


(Sus scrofa)		BDBM50358316
PNG
(CHEMBL1922545)
Show SMILES CC(C)(N(Cc1ccccc1)C(=O)C(F)(F)F)C(=O)NCCn1cc(COP(C)(=O)OC(C(F)(F)F)C(F)(F)F)nn1
Show InChI InChI=1S/C22H25F9N5O5P/c1-19(2,36(18(38)22(29,30)31)11-14-7-5-4-6-8-14)17(37)32-9-10-35-12-15(33-34-35)13-40-42(3,39)41-16(20(23,24)25)21(26,27)28/h4-8,12,16H,9-11,13H2,1-3H3,(H,32,37)
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n/an/a 1.45E+5n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of pig liver carboxylesterase using p-nitrophenyl acetate as substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Liver carboxylesterase


(Sus scrofa)		BDBM50358319
PNG
(CHEMBL1922548)
Show SMILES COC(=O)C(OP(C)(=O)OCc1cn(C[C@@H](NC(=O)CN(Cc2ccccc2)C(=O)C(F)(F)F)C(C)C)nn1)C(F)(F)F |r|
Show InChI InChI=1S/C24H30F6N5O7P/c1-15(2)18(31-19(36)13-34(22(38)24(28,29)30)10-16-8-6-5-7-9-16)12-35-11-17(32-33-35)14-41-43(4,39)42-20(21(37)40-3)23(25,26)27/h5-9,11,15,18,20H,10,12-14H2,1-4H3,(H,31,36)/t18-,20?,43?/m1/s1
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n/an/a 1.58E+5n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of pig liver carboxylesterase using p-nitrophenyl acetate as substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Liver carboxylesterase


(Sus scrofa)		BDBM50358317
PNG
(CHEMBL1922546)
Show SMILES C[C@@H](Cn1cc(COP(C)(=O)OC(C(F)(F)F)C(F)(F)F)nn1)NC(=O)CN(Cc1ccccc1)C(=O)C(F)(F)F |r|
Show InChI InChI=1S/C21H23F9N5O5P/c1-13(31-16(36)11-34(18(37)21(28,29)30)9-14-6-4-3-5-7-14)8-35-10-15(32-33-35)12-39-41(2,38)40-17(19(22,23)24)20(25,26)27/h3-7,10,13,17H,8-9,11-12H2,1-2H3,(H,31,36)/t13-,41?/m0/s1
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n/an/a 1.82E+5n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of pig liver carboxylesterase using p-nitrophenyl acetate as substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50358317
PNG
(CHEMBL1922546)
Show SMILES C[C@@H](Cn1cc(COP(C)(=O)OC(C(F)(F)F)C(F)(F)F)nn1)NC(=O)CN(Cc1ccccc1)C(=O)C(F)(F)F |r|
Show InChI InChI=1S/C21H23F9N5O5P/c1-13(31-16(36)11-34(18(37)21(28,29)30)9-14-6-4-3-5-7-14)8-35-10-15(32-33-35)12-39-41(2,38)40-17(19(22,23)24)20(25,26)27/h3-7,10,13,17H,8-9,11-12H2,1-2H3,(H,31,36)/t13-,41?/m0/s1
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n/an/a 2.18E+5n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of horse serum BChE incubated for 12 mins before addition of butyrylcholine iodide substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50358311
PNG
(CHEMBL1922540)
Show SMILES CP(=O)(OCC#C)OC(C(F)(F)F)C(F)(F)F
Show InChI InChI=1S/C7H7F6O3P/c1-3-4-15-17(2,14)16-5(6(8,9)10)7(11,12)13/h1,5H,4H2,2H3
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n/an/a 2.49E+5n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of horse serum BChE incubated for 12 mins before addition of butyrylcholine iodide substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50358314
PNG
(CHEMBL1922543)
Show SMILES CC(C)[C@@H](Cn1cc(COP(C)(=O)OC(C(F)(F)F)C(F)(F)F)nn1)NC(=O)CN(Cc1ccccc1)C(=O)[C@H](C)NC(=O)OC(C)(C)C |r|
Show InChI InChI=1S/C29H41F6N6O7P/c1-18(2)22(15-41-14-21(38-39-41)17-46-49(7,45)48-25(28(30,31)32)29(33,34)35)37-23(42)16-40(13-20-11-9-8-10-12-20)24(43)19(3)36-26(44)47-27(4,5)6/h8-12,14,18-19,22,25H,13,15-17H2,1-7H3,(H,36,44)(H,37,42)/t19-,22+,49?/m0/s1
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n/an/a 5.95E+5n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of horse serum BChE incubated for 12 mins before addition of butyrylcholine iodide substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50358315
PNG
(CHEMBL1922544)
Show SMILES CC[C@H](C)[C@@H](Cn1cc(COP(C)(=O)OC(C(F)(F)F)C(F)(F)F)nn1)NC(=O)CN(Cc1ccccc1)C(=O)C(F)(F)F |r|
Show InChI InChI=1S/C24H29F9N5O5P/c1-4-15(2)18(34-19(39)13-37(21(40)24(31,32)33)10-16-8-6-5-7-9-16)12-38-11-17(35-36-38)14-42-44(3,41)43-20(22(25,26)27)23(28,29)30/h5-9,11,15,18,20H,4,10,12-14H2,1-3H3,(H,34,39)/t15-,18+,44?/m0/s1
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n/an/a 7.02E+5n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of horse serum BChE incubated for 12 mins before addition of butyrylcholine iodide substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50358316
PNG
(CHEMBL1922545)
Show SMILES CC(C)(N(Cc1ccccc1)C(=O)C(F)(F)F)C(=O)NCCn1cc(COP(C)(=O)OC(C(F)(F)F)C(F)(F)F)nn1
Show InChI InChI=1S/C22H25F9N5O5P/c1-19(2,36(18(38)22(29,30)31)11-14-7-5-4-6-8-14)17(37)32-9-10-35-12-15(33-34-35)13-40-42(3,39)41-16(20(23,24)25)21(26,27)28/h4-8,12,16H,9-11,13H2,1-3H3,(H,32,37)
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n/an/a 7.46E+5n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of horse serum BChE incubated for 12 mins before addition of butyrylcholine iodide substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50358313
PNG
(CHEMBL1922542)
Show SMILES CC[C@H](C)[C@H](NC(=O)OC(C)(C)C)C(=O)N(Cc1ccc(OC)cc1OC)C(C)(C)C(=O)N[C@@H](C)Cn1cc(COP(C)(=O)OC(C(F)(F)F)C(F)(F)F)nn1 |r|
Show InChI InChI=1S/C34H51F6N6O9P/c1-12-20(2)26(42-30(49)54-31(4,5)6)27(47)46(17-22-13-14-24(51-9)15-25(22)52-10)32(7,8)29(48)41-21(3)16-45-18-23(43-44-45)19-53-56(11,50)55-28(33(35,36)37)34(38,39)40/h13-15,18,20-21,26,28H,12,16-17,19H2,1-11H3,(H,41,48)(H,42,49)/t20-,21-,26-,56?/m0/s1
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n/an/a 7.77E+5n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of horse serum BChE incubated for 12 mins before addition of butyrylcholine iodide substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Liver carboxylesterase


(Sus scrofa)		BDBM50358314
PNG
(CHEMBL1922543)
Show SMILES CC(C)[C@@H](Cn1cc(COP(C)(=O)OC(C(F)(F)F)C(F)(F)F)nn1)NC(=O)CN(Cc1ccccc1)C(=O)[C@H](C)NC(=O)OC(C)(C)C |r|
Show InChI InChI=1S/C29H41F6N6O7P/c1-18(2)22(15-41-14-21(38-39-41)17-46-49(7,45)48-25(28(30,31)32)29(33,34)35)37-23(42)16-40(13-20-11-9-8-10-12-20)24(43)19(3)36-26(44)47-27(4,5)6/h8-12,14,18-19,22,25H,13,15-17H2,1-7H3,(H,36,44)(H,37,42)/t19-,22+,49?/m0/s1
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n/an/a 7.85E+5n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of pig liver carboxylesterase using p-nitrophenyl acetate as substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Liver carboxylesterase


(Sus scrofa)		BDBM50358313
PNG
(CHEMBL1922542)
Show SMILES CC[C@H](C)[C@H](NC(=O)OC(C)(C)C)C(=O)N(Cc1ccc(OC)cc1OC)C(C)(C)C(=O)N[C@@H](C)Cn1cc(COP(C)(=O)OC(C(F)(F)F)C(F)(F)F)nn1 |r|
Show InChI InChI=1S/C34H51F6N6O9P/c1-12-20(2)26(42-30(49)54-31(4,5)6)27(47)46(17-22-13-14-24(51-9)15-25(22)52-10)32(7,8)29(48)41-21(3)16-45-18-23(43-44-45)19-53-56(11,50)55-28(33(35,36)37)34(38,39)40/h13-15,18,20-21,26,28H,12,16-17,19H2,1-11H3,(H,41,48)(H,42,49)/t20-,21-,26-,56?/m0/s1
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n/an/a 8.25E+5n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of pig liver carboxylesterase using p-nitrophenyl acetate as substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50358320
PNG
(CHEMBL1922549)
Show SMILES COC(=O)C(OP(C)(=O)OCc1cn(C[C@@H](NC(=O)CN(Cc2ccccc2)C(=O)[C@H](C)NC(=O)OC(C)(C)C)C(C)C)nn1)C(F)(F)F |r|
Show InChI InChI=1S/C30H44F3N6O9P/c1-19(2)23(16-39-15-22(36-37-39)18-46-49(8,44)48-25(27(42)45-7)30(31,32)33)35-24(40)17-38(14-21-12-10-9-11-13-21)26(41)20(3)34-28(43)47-29(4,5)6/h9-13,15,19-20,23,25H,14,16-18H2,1-8H3,(H,34,43)(H,35,40)/t20-,23+,25?,49?/m0/s1
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n/an/a 9.60E+5n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of horse serum BChE incubated for 12 mins before addition of butyrylcholine iodide substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50358318
PNG
(CHEMBL1922547)
Show SMILES CC(C)[C@@H](Cn1cc(COP(C)(=O)OC(C(F)(F)F)C(F)(F)F)nn1)NC(=O)CN(Cc1ccccc1)C(=O)C(F)(F)F |r|
Show InChI InChI=1S/C23H27F9N5O5P/c1-14(2)17(33-18(38)12-36(20(39)23(30,31)32)9-15-7-5-4-6-8-15)11-37-10-16(34-35-37)13-41-43(3,40)42-19(21(24,25)26)22(27,28)29/h4-8,10,14,17,19H,9,11-13H2,1-3H3,(H,33,38)/t17-,43?/m1/s1
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n/an/a 1.10E+6n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of horse serum BChE incubated for 12 mins before addition of butyrylcholine iodide substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
Cholinesterase


(Equus caballus (Horse))		BDBM50358319
PNG
(CHEMBL1922548)
Show SMILES COC(=O)C(OP(C)(=O)OCc1cn(C[C@@H](NC(=O)CN(Cc2ccccc2)C(=O)C(F)(F)F)C(C)C)nn1)C(F)(F)F |r|
Show InChI InChI=1S/C24H30F6N5O7P/c1-15(2)18(31-19(36)13-34(22(38)24(28,29)30)10-16-8-6-5-7-9-16)12-35-11-17(32-33-35)14-41-43(4,39)42-20(21(37)40-3)23(25,26)27/h5-9,11,15,18,20H,10,12-14H2,1-4H3,(H,31,36)/t18-,20?,43?/m1/s1
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n/an/a 2.00E+6n/an/an/an/an/an/a



Moscow State University

Curated by ChEMBL


Assay Description
Inhibition of horse serum BChE incubated for 12 mins before addition of butyrylcholine iodide substrate by spectrophotometric analysis

Bioorg Med Chem Lett 21: 7216-8 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.030
BindingDB Entry DOI: 10.7270/Q2W66M65
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%