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Compile Data Set for Download or QSAR

Found 45 hits with Last Name = 'gómez-cañas' 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
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM21281
PNG
((11R)-2-methyl-11-(morpholin-4-ylmethyl)-3-(naphth...)
Show SMILES Cc1c(C(=O)c2cccc3ccccc23)c2cccc3OC[C@@H](CN4CCOCC4)n1c23 |r|
Show InChI InChI=1S/C27H26N2O3/c1-18-25(27(30)22-9-4-7-19-6-2-3-8-21(19)22)23-10-5-11-24-26(23)29(18)20(17-32-24)16-28-12-14-31-15-13-28/h2-11,20H,12-17H2,1H3/t20-/m1/s1
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3.70n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM21278
PNG
(5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl...)
Show SMILES Cc1c(nn(c1-c1ccc(Cl)cc1)-c1ccc(Cl)cc1Cl)C(=O)NN1CCCCC1
Show InChI InChI=1S/C22H21Cl3N4O/c1-14-20(22(30)27-28-11-3-2-4-12-28)26-29(19-10-9-17(24)13-18(19)25)21(14)15-5-7-16(23)8-6-15/h5-10,13H,2-4,11-12H2,1H3,(H,27,30)
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7.30n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM21281
PNG
((11R)-2-methyl-11-(morpholin-4-ylmethyl)-3-(naphth...)
Show SMILES Cc1c(C(=O)c2cccc3ccccc23)c2cccc3OC[C@@H](CN4CCOCC4)n1c23 |r|
Show InChI InChI=1S/C27H26N2O3/c1-18-25(27(30)22-9-4-7-19-6-2-3-8-21(19)22)23-10-5-11-24-26(23)29(18)20(17-32-24)16-28-12-14-31-15-13-28/h2-11,20H,12-17H2,1H3/t20-/m1/s1
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46n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50431807
PNG
(CHEMBL2347041)
Show SMILES CCCCCc1cc(-c2ccc(Cl)cc2)n(n1)-c1ccc(Cl)cc1Cl
Show InChI InChI=1S/C20H19Cl3N2/c1-2-3-4-5-17-13-20(14-6-8-15(21)9-7-14)25(24-17)19-11-10-16(22)12-18(19)23/h6-13H,2-5H2,1H3
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458n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50147009
PNG
(5-(4-Chloro-phenyl)-1-(2,4-dichloro-phenyl)-3-hexy...)
Show SMILES CCCCCCc1nc(-c2ccc(Cl)cc2)n(n1)-c1ccc(Cl)cc1Cl
Show InChI InChI=1S/C20H20Cl3N3/c1-2-3-4-5-6-19-24-20(14-7-9-15(21)10-8-14)26(25-19)18-12-11-16(22)13-17(18)23/h7-13H,2-6H2,1H3
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829n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50431808
PNG
(CHEMBL2347040)
Show SMILES CCCCCc1cc(-c2ccccc2)n(n1)-c1ccccc1
Show InChI InChI=1S/C20H22N2/c1-2-3-6-13-18-16-20(17-11-7-4-8-12-17)22(21-18)19-14-9-5-10-15-19/h4-5,7-12,14-16H,2-3,6,13H2,1H3
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2.94E+3n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50147009
PNG
(5-(4-Chloro-phenyl)-1-(2,4-dichloro-phenyl)-3-hexy...)
Show SMILES CCCCCCc1nc(-c2ccc(Cl)cc2)n(n1)-c1ccc(Cl)cc1Cl
Show InChI InChI=1S/C20H20Cl3N3/c1-2-3-4-5-6-19-24-20(14-7-9-15(21)10-8-14)26(25-19)18-12-11-16(22)13-17(18)23/h7-13H,2-6H2,1H3
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3.08E+3n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50431803
PNG
(CHEMBL2347045)
Show SMILES O=C(NN1CCCCC1)c1cc(-c2ccccc2)n(n1)-c1ccccc1
Show InChI InChI=1S/C21H22N4O/c26-21(23-24-14-8-3-9-15-24)19-16-20(17-10-4-1-5-11-17)25(22-19)18-12-6-2-7-13-18/h1-2,4-7,10-13,16H,3,8-9,14-15H2,(H,23,26)
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4.59E+3n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50431808
PNG
(CHEMBL2347040)
Show SMILES CCCCCc1cc(-c2ccccc2)n(n1)-c1ccccc1
Show InChI InChI=1S/C20H22N2/c1-2-3-6-13-18-16-20(17-11-7-4-8-12-17)22(21-18)19-14-9-5-10-15-19/h4-5,7-12,14-16H,2-3,6,13H2,1H3
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6.16E+3n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50431800
PNG
(CHEMBL2347048)
Show SMILES Cc1c(nn(c1-c1ccccc1)-c1ccccc1)C(=O)NN1CCCCC1
Show InChI InChI=1S/C22H24N4O/c1-17-20(22(27)24-25-15-9-4-10-16-25)23-26(19-13-7-3-8-14-19)21(17)18-11-5-2-6-12-18/h2-3,5-8,11-14H,4,9-10,15-16H2,1H3,(H,24,27)
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9.69E+3n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50431804
PNG
(CHEMBL2347044)
Show SMILES CCCCCCCCCCCCCCCCNC(=O)c1cc(-c2ccccc2)n(n1)-c1ccccc1
Show InChI InChI=1S/C32H45N3O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-21-26-33-32(36)30-27-31(28-22-17-15-18-23-28)35(34-30)29-24-19-16-20-25-29/h15-20,22-25,27H,2-14,21,26H2,1H3,(H,33,36)
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>1.00E+4n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50431798
PNG
(CHEMBL2347050)
Show SMILES CCCCCCCCCCCCCCCCNC(=O)c1nc(-c2ccc(Cl)cc2)n(n1)-c1ccc(Cl)cc1
Show InChI InChI=1S/C31H42Cl2N4O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-24-34-31(38)29-35-30(25-16-18-26(32)19-17-25)37(36-29)28-22-20-27(33)21-23-28/h16-23H,2-15,24H2,1H3,(H,34,38)
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>1.00E+4n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50431801
PNG
(CHEMBL2347047)
Show SMILES CCCCCCCCCCCCCCCCNC(=O)c1nn(c(c1C)-c1ccccc1)-c1ccccc1
Show InChI InChI=1S/C33H47N3O/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-22-27-34-33(37)31-28(2)32(29-23-18-16-19-24-29)36(35-31)30-25-20-17-21-26-30/h16-21,23-26H,3-15,22,27H2,1-2H3,(H,34,37)
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>1.00E+4n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50431801
PNG
(CHEMBL2347047)
Show SMILES CCCCCCCCCCCCCCCCNC(=O)c1nn(c(c1C)-c1ccccc1)-c1ccccc1
Show InChI InChI=1S/C33H47N3O/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-22-27-34-33(37)31-28(2)32(29-23-18-16-19-24-29)36(35-31)30-25-20-17-21-26-30/h16-21,23-26H,3-15,22,27H2,1-2H3,(H,34,37)
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>1.00E+4n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50431798
PNG
(CHEMBL2347050)
Show SMILES CCCCCCCCCCCCCCCCNC(=O)c1nc(-c2ccc(Cl)cc2)n(n1)-c1ccc(Cl)cc1
Show InChI InChI=1S/C31H42Cl2N4O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-24-34-31(38)29-35-30(25-16-18-26(32)19-17-25)37(36-29)28-22-20-27(33)21-23-28/h16-23H,2-15,24H2,1H3,(H,34,38)
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>1.00E+4n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50431800
PNG
(CHEMBL2347048)
Show SMILES Cc1c(nn(c1-c1ccccc1)-c1ccccc1)C(=O)NN1CCCCC1
Show InChI InChI=1S/C22H24N4O/c1-17-20(22(27)24-25-15-9-4-10-16-25)23-26(19-13-7-3-8-14-19)21(17)18-11-5-2-6-12-18/h2-3,5-8,11-14H,4,9-10,15-16H2,1H3,(H,24,27)
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1.82E+4n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50431803
PNG
(CHEMBL2347045)
Show SMILES O=C(NN1CCCCC1)c1cc(-c2ccccc2)n(n1)-c1ccccc1
Show InChI InChI=1S/C21H22N4O/c26-21(23-24-14-8-3-9-15-24)19-16-20(17-10-4-1-5-11-17)25(22-19)18-12-6-2-7-13-18/h1-2,4-7,10-13,16H,3,8-9,14-15H2,(H,23,26)
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2.79E+4n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50431807
PNG
(CHEMBL2347041)
Show SMILES CCCCCc1cc(-c2ccc(Cl)cc2)n(n1)-c1ccc(Cl)cc1Cl
Show InChI InChI=1S/C20H19Cl3N2/c1-2-3-4-5-17-13-20(14-6-8-15(21)9-7-14)25(24-17)19-11-10-16(22)12-18(19)23/h6-13H,2-5H2,1H3
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>4.00E+4n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50431806
PNG
(CHEMBL2347042)
Show SMILES CCCCCCc1cc(-c2ccc(Cl)cc2)n(n1)-c1ccc(Cl)cc1Cl
Show InChI InChI=1S/C21H21Cl3N2/c1-2-3-4-5-6-18-14-21(15-7-9-16(22)10-8-15)26(25-18)20-12-11-17(23)13-19(20)24/h7-14H,2-6H2,1H3
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>4.00E+4n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50431805
PNG
(CHEMBL2347043)
Show SMILES CCCCCCCC\C=C/CCCCCCCCNC(=O)c1cc(-c2ccccc2)n(n1)-c1ccccc1
Show InChI InChI=1S/C34H47N3O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-23-28-35-34(38)32-29-33(30-24-19-17-20-25-30)37(36-32)31-26-21-18-22-27-31/h9-10,17-22,24-27,29H,2-8,11-16,23,28H2,1H3,(H,35,38)/b10-9-
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>4.00E+4n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50431804
PNG
(CHEMBL2347044)
Show SMILES CCCCCCCCCCCCCCCCNC(=O)c1cc(-c2ccccc2)n(n1)-c1ccccc1
Show InChI InChI=1S/C32H45N3O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-21-26-33-32(36)30-27-31(28-22-17-15-18-23-28)35(34-30)29-24-19-16-20-25-29/h15-20,22-25,27H,2-14,21,26H2,1H3,(H,33,36)
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>4.00E+4n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50431802
PNG
(CHEMBL2347046)
Show SMILES CCCCCCCC\C=C/CCCCCCCCNC(=O)c1nn(c(c1C)-c1ccccc1)-c1ccccc1
Show InChI InChI=1S/C35H49N3O/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-24-29-36-35(39)33-30(2)34(31-25-20-18-21-26-31)38(37-33)32-27-22-19-23-28-32/h10-11,18-23,25-28H,3-9,12-17,24,29H2,1-2H3,(H,36,39)/b11-10-
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Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50431799
PNG
(CHEMBL2347049)
Show SMILES CCCCCCCC\C=C/CCCCCCCCNC(=O)c1nc(-c2ccc(Cl)cc2)n(n1)-c1ccc(Cl)cc1
Show InChI InChI=1S/C33H44Cl2N4O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-26-36-33(40)31-37-32(27-18-20-28(34)21-19-27)39(38-31)30-24-22-29(35)23-25-30/h9-10,18-25H,2-8,11-17,26H2,1H3,(H,36,40)/b10-9-
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Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50431806
PNG
(CHEMBL2347042)
Show SMILES CCCCCCc1cc(-c2ccc(Cl)cc2)n(n1)-c1ccc(Cl)cc1Cl
Show InChI InChI=1S/C21H21Cl3N2/c1-2-3-4-5-6-18-14-21(15-7-9-16(22)10-8-15)26(25-18)20-12-11-17(23)13-19(20)24/h7-14H,2-6H2,1H3
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Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50431805
PNG
(CHEMBL2347043)
Show SMILES CCCCCCCC\C=C/CCCCCCCCNC(=O)c1cc(-c2ccccc2)n(n1)-c1ccccc1
Show InChI InChI=1S/C34H47N3O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-23-28-35-34(38)32-29-33(30-24-19-17-20-25-30)37(36-32)31-26-21-18-22-27-31/h9-10,17-22,24-27,29H,2-8,11-16,23,28H2,1H3,(H,35,38)/b10-9-
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Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50431802
PNG
(CHEMBL2347046)
Show SMILES CCCCCCCC\C=C/CCCCCCCCNC(=O)c1nn(c(c1C)-c1ccccc1)-c1ccccc1
Show InChI InChI=1S/C35H49N3O/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-24-29-36-35(39)33-30(2)34(31-25-20-18-21-26-31)38(37-33)32-27-22-19-23-28-32/h10-11,18-23,25-28H,3-9,12-17,24,29H2,1-2H3,(H,36,39)/b11-10-
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Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50431799
PNG
(CHEMBL2347049)
Show SMILES CCCCCCCC\C=C/CCCCCCCCNC(=O)c1nc(-c2ccc(Cl)cc2)n(n1)-c1ccc(Cl)cc1
Show InChI InChI=1S/C33H44Cl2N4O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-26-36-33(40)31-37-32(27-18-20-28(34)21-19-27)39(38-31)30-24-22-29(35)23-25-30/h9-10,18-25H,2-8,11-17,26H2,1H3,(H,36,40)/b10-9-
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Instituto de Qu£mica M£dica

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor after 90 mins by liquid scintillation spectrophotometer analysis


Bioorg Med Chem 21: 1708-16 (2013)


Article DOI: 10.1016/j.bmc.2013.01.055
BindingDB Entry DOI: 10.7270/Q2MG7QW1
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50447027
PNG
(CHEMBL3116284)
Show SMILES C(Cn1nc(OCc2cccc3ccccc23)c2ccccc12)N1CCCCC1
Show InChI InChI=1S/C25H27N3O/c1-6-15-27(16-7-1)17-18-28-24-14-5-4-13-23(24)25(26-28)29-19-21-11-8-10-20-9-2-3-12-22(20)21/h2-5,8-14H,1,6-7,15-19H2
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n/an/a 910n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's method


Eur J Med Chem 73: 56-72 (2014)


Article DOI: 10.1016/j.ejmech.2013.11.026
BindingDB Entry DOI: 10.7270/Q2474CC8
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50447026
PNG
(CHEMBL3116286)
Show SMILES C(Cn1nc(OCc2ccc3ccccc3c2)c2ccccc12)N1CCCCC1
Show InChI InChI=1S/C25H27N3O/c1-6-14-27(15-7-1)16-17-28-24-11-5-4-10-23(24)25(26-28)29-19-20-12-13-21-8-2-3-9-22(21)18-20/h2-5,8-13,18H,1,6-7,14-17,19H2
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n/an/a 1.40E+3n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's method


Eur J Med Chem 73: 56-72 (2014)


Article DOI: 10.1016/j.ejmech.2013.11.026
BindingDB Entry DOI: 10.7270/Q2474CC8
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50447015
PNG
(CHEMBL3116300)
Show SMILES Nc1ccc2n(CCN3CCCCC3)nc(OCc3ccc4ccccc4c3)c2c1
Show InChI InChI=1S/C25H28N4O/c26-22-10-11-24-23(17-22)25(27-29(24)15-14-28-12-4-1-5-13-28)30-18-19-8-9-20-6-2-3-7-21(20)16-19/h2-3,6-11,16-17H,1,4-5,12-15,18,26H2
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n/an/a 1.50E+3n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's method


Eur J Med Chem 73: 56-72 (2014)


Article DOI: 10.1016/j.ejmech.2013.11.026
BindingDB Entry DOI: 10.7270/Q2474CC8
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50447020
PNG
(CHEMBL3116294)
Show SMILES [O-][N+](=O)c1ccc2n(CCN3CCCCC3)nc(OCc3ccc4ccccc4c3)c2c1
Show InChI InChI=1S/C25H26N4O3/c30-29(31)22-10-11-24-23(17-22)25(26-28(24)15-14-27-12-4-1-5-13-27)32-18-19-8-9-20-6-2-3-7-21(20)16-19/h2-3,6-11,16-17H,1,4-5,12-15,18H2
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n/an/a 2.07E+3n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's method


Eur J Med Chem 73: 56-72 (2014)


Article DOI: 10.1016/j.ejmech.2013.11.026
BindingDB Entry DOI: 10.7270/Q2474CC8
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50447030
PNG
(CHEMBL3116280)
Show SMILES COc1ccc(COc2nn(CCN(C(C)C)C(C)C)c3ccccc23)cc1
Show InChI InChI=1S/C23H31N3O2/c1-17(2)25(18(3)4)14-15-26-22-9-7-6-8-21(22)23(24-26)28-16-19-10-12-20(27-5)13-11-19/h6-13,17-18H,14-16H2,1-5H3
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n/an/a 2.28E+3n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's method


Eur J Med Chem 73: 56-72 (2014)


Article DOI: 10.1016/j.ejmech.2013.11.026
BindingDB Entry DOI: 10.7270/Q2474CC8
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(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 2.50E+3n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's method


Eur J Med Chem 73: 56-72 (2014)


Article DOI: 10.1016/j.ejmech.2013.11.026
BindingDB Entry DOI: 10.7270/Q2474CC8
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50447028
PNG
(CHEMBL3116283)
Show SMILES C(Cn1nc(OCc2cccc3ccccc23)c2ccccc12)N1CCCC1
Show InChI InChI=1S/C24H25N3O/c1-2-11-21-19(8-1)9-7-10-20(21)18-28-24-22-12-3-4-13-23(22)27(25-24)17-16-26-14-5-6-15-26/h1-4,7-13H,5-6,14-18H2
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n/an/a 6.70E+3n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's method


Eur J Med Chem 73: 56-72 (2014)


Article DOI: 10.1016/j.ejmech.2013.11.026
BindingDB Entry DOI: 10.7270/Q2474CC8
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50447021
PNG
(CHEMBL3116293)
Show SMILES CCCCCn1nc(OCc2ccc3ccccc3c2)c2cc(ccc12)[N+]([O-])=O
Show InChI InChI=1S/C23H23N3O3/c1-2-3-6-13-25-22-12-11-20(26(27)28)15-21(22)23(24-25)29-16-17-9-10-18-7-4-5-8-19(18)14-17/h4-5,7-12,14-15H,2-3,6,13,16H2,1H3
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n/an/a>1.00E+4n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's method


Eur J Med Chem 73: 56-72 (2014)


Article DOI: 10.1016/j.ejmech.2013.11.026
BindingDB Entry DOI: 10.7270/Q2474CC8
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50447022
PNG
(CHEMBL3116289)
Show SMILES CCCCCn1nc(OCc2ccc(OC)cc2)c2cc(ccc12)[N+]([O-])=O
Show InChI InChI=1S/C20H23N3O4/c1-3-4-5-12-22-19-11-8-16(23(24)25)13-18(19)20(21-22)27-14-15-6-9-17(26-2)10-7-15/h6-11,13H,3-5,12,14H2,1-2H3
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n/an/a>1.00E+4n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's method


Eur J Med Chem 73: 56-72 (2014)


Article DOI: 10.1016/j.ejmech.2013.11.026
BindingDB Entry DOI: 10.7270/Q2474CC8
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50447023
PNG
(CHEMBL1973869)
Show SMILES [O-][N+](=O)c1ccc2n(Cc3ccccc3)nc(OCc3ccccc3)c2c1
Show InChI InChI=1S/C21H17N3O3/c25-24(26)18-11-12-20-19(13-18)21(27-15-17-9-5-2-6-10-17)22-23(20)14-16-7-3-1-4-8-16/h1-13H,14-15H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's method


Eur J Med Chem 73: 56-72 (2014)


Article DOI: 10.1016/j.ejmech.2013.11.026
BindingDB Entry DOI: 10.7270/Q2474CC8
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50447024
PNG
(CHEMBL3116288)
Show SMILES [O-][N+](=O)c1ccc2n(Cc3ccccc3)nc(OCC3CCCCC3)c2c1
Show InChI InChI=1S/C21H23N3O3/c25-24(26)18-11-12-20-19(13-18)21(27-15-17-9-5-2-6-10-17)22-23(20)14-16-7-3-1-4-8-16/h1,3-4,7-8,11-13,17H,2,5-6,9-10,14-15H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's method


Eur J Med Chem 73: 56-72 (2014)


Article DOI: 10.1016/j.ejmech.2013.11.026
BindingDB Entry DOI: 10.7270/Q2474CC8
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50447018
PNG
(CHEMBL3116296)
Show SMILES [O-][N+](=O)c1ccc2n(Cc3ccccc3)nc(OCc3ccc4ccccc4c3)c2c1
Show InChI InChI=1S/C25H19N3O3/c29-28(30)22-12-13-24-23(15-22)25(26-27(24)16-18-6-2-1-3-7-18)31-17-19-10-11-20-8-4-5-9-21(20)14-19/h1-15H,16-17H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's method


Eur J Med Chem 73: 56-72 (2014)


Article DOI: 10.1016/j.ejmech.2013.11.026
BindingDB Entry DOI: 10.7270/Q2474CC8
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50447016
PNG
(CHEMBL3116298)
Show SMILES Nc1ccc2n(Cc3ccccc3)nc(OCc3ccccc3)c2c1
Show InChI InChI=1S/C21H19N3O/c22-18-11-12-20-19(13-18)21(25-15-17-9-5-2-6-10-17)23-24(20)14-16-7-3-1-4-8-16/h1-13H,14-15,22H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's method


Eur J Med Chem 73: 56-72 (2014)


Article DOI: 10.1016/j.ejmech.2013.11.026
BindingDB Entry DOI: 10.7270/Q2474CC8
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50447029
PNG
(CHEMBL3116281)
Show SMILES COc1ccc(COc2nn(Cc3ccc(OC)cc3)c3ccccc23)cc1
Show InChI InChI=1S/C23H22N2O3/c1-26-19-11-7-17(8-12-19)15-25-22-6-4-3-5-21(22)23(24-25)28-16-18-9-13-20(27-2)14-10-18/h3-14H,15-16H2,1-2H3
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n/an/a>1.00E+4n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's method


Eur J Med Chem 73: 56-72 (2014)


Article DOI: 10.1016/j.ejmech.2013.11.026
BindingDB Entry DOI: 10.7270/Q2474CC8
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50447031
PNG
(CHEMBL3116278)
Show SMILES C(Oc1nn(CC2CCCCC2)c2ccccc12)C1CCCCC1
Show InChI InChI=1S/C21H30N2O/c1-3-9-17(10-4-1)15-23-20-14-8-7-13-19(20)21(22-23)24-16-18-11-5-2-6-12-18/h7-8,13-14,17-18H,1-6,9-12,15-16H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's method


Eur J Med Chem 73: 56-72 (2014)


Article DOI: 10.1016/j.ejmech.2013.11.026
BindingDB Entry DOI: 10.7270/Q2474CC8
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50447017
PNG
(CHEMBL3116297)
Show SMILES [O-][N+](=O)c1ccc2n(Cc3ccc4ccccc4c3)nc(OCc3ccc4ccccc4c3)c2c1
Show InChI InChI=1S/C29H21N3O3/c33-32(34)26-13-14-28-27(17-26)29(35-19-21-10-12-23-6-2-4-8-25(23)16-21)30-31(28)18-20-9-11-22-5-1-3-7-24(22)15-20/h1-17H,18-19H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's method


Eur J Med Chem 73: 56-72 (2014)


Article DOI: 10.1016/j.ejmech.2013.11.026
BindingDB Entry DOI: 10.7270/Q2474CC8
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50447019
PNG
(CHEMBL3116295)
Show SMILES [O-][N+](=O)c1ccc2n(CCN3CCOCC3)nc(OCc3ccc4ccccc4c3)c2c1
Show InChI InChI=1S/C24H24N4O4/c29-28(30)21-7-8-23-22(16-21)24(25-27(23)10-9-26-11-13-31-14-12-26)32-17-18-5-6-19-3-1-2-4-20(19)15-18/h1-8,15-16H,9-14,17H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's method


Eur J Med Chem 73: 56-72 (2014)


Article DOI: 10.1016/j.ejmech.2013.11.026
BindingDB Entry DOI: 10.7270/Q2474CC8
More data for this
Ligand-Target Pair
Butyrylcholinesterase (BuChE)


(Equus caballus (Horse))
BDBM50447025
PNG
(CHEMBL3116287)
Show SMILES CCCCCOc1nn(CCCCC)c2ccc(cc12)[N+]([O-])=O
Show InChI InChI=1S/C17H25N3O3/c1-3-5-7-11-19-16-10-9-14(20(21)22)13-15(16)17(18-19)23-12-8-6-4-2/h9-10,13H,3-8,11-12H2,1-2H3
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n/an/a>1.00E+4n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (CSIC)

Curated by ChEMBL


Assay Description
Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's method


Eur J Med Chem 73: 56-72 (2014)


Article DOI: 10.1016/j.ejmech.2013.11.026
BindingDB Entry DOI: 10.7270/Q2474CC8
More data for this
Ligand-Target Pair