Found 68 hits of Enzyme Inhibition Constant Data Target/Host
(Institution) | Ligand | Target/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 | pH | Temp
°C |
|---|
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301869
(7-(2-(trifluoromethyl)phenyl)-N-(4-(trifluoromethy...)Show SMILES FC(F)(F)c1ccc(Nc2noc3c(cccc23)-c2ccccc2C(F)(F)F)cc1 Show InChI InChI=1S/C21H12F6N2O/c22-20(23,24)12-8-10-13(11-9-12)28-19-16-6-3-5-15(18(16)30-29-19)14-4-1-2-7-17(14)21(25,26)27/h1-11H,(H,28,29) | PDB
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| n/a | n/a | 4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301856
(7-(trifluoromethyl)-N-(4-(trifluoromethyl)phenyl)b...)Show InChI InChI=1S/C15H8F6N2O/c16-14(17,18)8-4-6-9(7-5-8)22-13-10-2-1-3-11(15(19,20)21)12(10)24-23-13/h1-7H,(H,22,23) | PDB
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| n/a | n/a | 4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301871
(7-(1H-indol-5-yl)-N-(4-(trifluoromethyl)phenyl)ben...)Show SMILES FC(F)(F)c1ccc(Nc2noc3c(cccc23)-c2ccc3[nH]ccc3c2)cc1 Show InChI InChI=1S/C22H14F3N3O/c23-22(24,25)15-5-7-16(8-6-15)27-21-18-3-1-2-17(20(18)29-28-21)13-4-9-19-14(12-13)10-11-26-19/h1-12,26H,(H,27,28) | PDB
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| n/a | n/a | 8 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301859
(6-(2-(trifluoromethyl)phenyl)-N-(4-(trifluoromethy...)Show SMILES FC(F)(F)c1ccc(Nc2noc3cc(ccc23)-c2ccccc2C(F)(F)F)cc1 Show InChI InChI=1S/C21H12F6N2O/c22-20(23,24)13-6-8-14(9-7-13)28-19-16-10-5-12(11-18(16)30-29-19)15-3-1-2-4-17(15)21(25,26)27/h1-11H,(H,28,29) | PDB
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| n/a | n/a | 8 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301870
(7-(3-(trifluoromethyl)phenyl)-N-(4-(trifluoromethy...)Show SMILES FC(F)(F)c1ccc(Nc2noc3c(cccc23)-c2cccc(c2)C(F)(F)F)cc1 Show InChI InChI=1S/C21H12F6N2O/c22-20(23,24)13-7-9-15(10-8-13)28-19-17-6-2-5-16(18(17)30-29-19)12-3-1-4-14(11-12)21(25,26)27/h1-11H,(H,28,29) | PDB
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| n/a | n/a | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301857
(6-(trifluoromethyl)-N-(4-(trifluoromethyl)phenyl)b...)Show InChI InChI=1S/C15H8F6N2O/c16-14(17,18)8-1-4-10(5-2-8)22-13-11-6-3-9(15(19,20)21)7-12(11)24-23-13/h1-7H,(H,22,23) | PDB
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| n/a | n/a | 18 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301867
(6-(pyridin-4-yl)-N-(4-(trifluoromethyl)phenyl)benz...)Show SMILES FC(F)(F)c1ccc(Nc2noc3cc(ccc23)-c2ccncc2)cc1 Show InChI InChI=1S/C19H12F3N3O/c20-19(21,22)14-2-4-15(5-3-14)24-18-16-6-1-13(11-17(16)26-25-18)12-7-9-23-10-8-12/h1-11H,(H,24,25) | PDB
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| n/a | n/a | 19 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301872
(7-(trifluoromethyl)-N-(4-(trifluoromethyl)phenyl)i...)Show InChI InChI=1S/C14H7F6N3O/c15-13(16,17)7-1-3-8(4-2-7)22-12-9-5-6-21-11(14(18,19)20)10(9)24-23-12/h1-6H,(H,22,23) | PDB
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| n/a | n/a | 19 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301860
(6-(isoquinolin-5-yl)-N-(4-(trifluoromethyl)phenyl)...)Show SMILES FC(F)(F)c1ccc(Nc2noc3cc(ccc23)-c2cccc3cnccc23)cc1 Show InChI InChI=1S/C23H14F3N3O/c24-23(25,26)16-5-7-17(8-6-16)28-22-20-9-4-14(12-21(20)30-29-22)18-3-1-2-15-13-27-11-10-19(15)18/h1-13H,(H,28,29) | PDB
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| n/a | n/a | 19 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301866
(6-(pyridin-3-yl)-N-(4-(trifluoromethyl)phenyl)benz...)Show SMILES FC(F)(F)c1ccc(Nc2noc3cc(ccc23)-c2cccnc2)cc1 Show InChI InChI=1S/C19H12F3N3O/c20-19(21,22)14-4-6-15(7-5-14)24-18-16-8-3-12(10-17(16)26-25-18)13-2-1-9-23-11-13/h1-11H,(H,24,25) | PDB
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| n/a | n/a | 20 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301866
(6-(pyridin-3-yl)-N-(4-(trifluoromethyl)phenyl)benz...)Show SMILES FC(F)(F)c1ccc(Nc2noc3cc(ccc23)-c2cccnc2)cc1 Show InChI InChI=1S/C19H12F3N3O/c20-19(21,22)14-4-6-15(7-5-14)24-18-16-8-3-12(10-17(16)26-25-18)13-2-1-9-23-11-13/h1-11H,(H,24,25) | PDB
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| n/a | n/a | 23 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301873
(CHEMBL576719 | N-(4-(trifluoromethyl)phenyl)benzo[...)Show InChI InChI=1S/C14H9F3N2O/c15-14(16,17)9-5-7-10(8-6-9)18-13-11-3-1-2-4-12(11)20-19-13/h1-8H,(H,18,19) | PDB
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| n/a | n/a | 25 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301893
(CHEMBL578566 | N-(4-(trifluoromethyl)phenyl)isoxaz...)Show InChI InChI=1S/C13H8F3N3O/c14-13(15,16)8-3-5-9(6-4-8)18-11-10-2-1-7-17-12(10)20-19-11/h1-7H,(H,18,19) | PDB
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| n/a | n/a | 27 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301860
(6-(isoquinolin-5-yl)-N-(4-(trifluoromethyl)phenyl)...)Show SMILES FC(F)(F)c1ccc(Nc2noc3cc(ccc23)-c2cccc3cnccc23)cc1 Show InChI InChI=1S/C23H14F3N3O/c24-23(25,26)16-5-7-17(8-6-16)28-22-20-9-4-14(12-21(20)30-29-22)18-3-1-2-15-13-27-11-10-19(15)18/h1-13H,(H,28,29) | PDB
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| n/a | n/a | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301894
(CHEMBL578770 | N-(4-(trifluoromethyl)phenyl)isoxaz...)Show InChI InChI=1S/C13H8F3N3O/c14-13(15,16)8-1-3-9(4-2-8)18-12-10-5-6-17-7-11(10)20-19-12/h1-7H,(H,18,19) | PDB
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| n/a | n/a | 31 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301858
(5-(trifluoromethyl)-N-(4-(trifluoromethyl)phenyl)b...)Show InChI InChI=1S/C15H8F6N2O/c16-14(17,18)8-1-4-10(5-2-8)22-13-11-7-9(15(19,20)21)3-6-12(11)24-23-13/h1-7H,(H,22,23) | PDB
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| n/a | n/a | 40 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301871
(7-(1H-indol-5-yl)-N-(4-(trifluoromethyl)phenyl)ben...)Show SMILES FC(F)(F)c1ccc(Nc2noc3c(cccc23)-c2ccc3[nH]ccc3c2)cc1 Show InChI InChI=1S/C22H14F3N3O/c23-22(24,25)15-5-7-16(8-6-15)27-21-18-3-1-2-17(20(18)29-28-21)13-4-9-19-14(12-13)10-11-26-19/h1-12,26H,(H,27,28) | PDB
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| n/a | n/a | 41 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301865
(6-(2-fluorophenyl)-N-(4-(trifluoromethyl)phenyl)be...)Show SMILES Fc1ccccc1-c1ccc2c(Nc3ccc(cc3)C(F)(F)F)noc2c1 Show InChI InChI=1S/C20H12F4N2O/c21-17-4-2-1-3-15(17)12-5-10-16-18(11-12)27-26-19(16)25-14-8-6-13(7-9-14)20(22,23)24/h1-11H,(H,25,26) | PDB
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| n/a | n/a | 55 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301867
(6-(pyridin-4-yl)-N-(4-(trifluoromethyl)phenyl)benz...)Show SMILES FC(F)(F)c1ccc(Nc2noc3cc(ccc23)-c2ccncc2)cc1 Show InChI InChI=1S/C19H12F3N3O/c20-19(21,22)14-2-4-15(5-3-14)24-18-16-6-1-13(11-17(16)26-25-18)12-7-9-23-10-8-12/h1-11H,(H,24,25) | PDB
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| n/a | n/a | 58 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301874
(CHEMBL578048 | N-(4-(trifluoromethoxy)phenyl)benzo...)Show InChI InChI=1S/C14H9F3N2O2/c15-14(16,17)20-10-7-5-9(6-8-10)18-13-11-3-1-2-4-12(11)21-19-13/h1-8H,(H,18,19) | PDB
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| n/a | n/a | 60 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301861
(6-(1H-indol-5-yl)-N-(4-(trifluoromethyl)phenyl)ben...)Show SMILES FC(F)(F)c1ccc(Nc2noc3cc(ccc23)-c2ccc3[nH]ccc3c2)cc1 Show InChI InChI=1S/C22H14F3N3O/c23-22(24,25)16-3-5-17(6-4-16)27-21-18-7-1-14(12-20(18)29-28-21)13-2-8-19-15(11-13)9-10-26-19/h1-12,26H,(H,27,28) | PDB
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| n/a | n/a | 70 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301859
(6-(2-(trifluoromethyl)phenyl)-N-(4-(trifluoromethy...)Show SMILES FC(F)(F)c1ccc(Nc2noc3cc(ccc23)-c2ccccc2C(F)(F)F)cc1 Show InChI InChI=1S/C21H12F6N2O/c22-20(23,24)13-6-8-14(9-7-13)28-19-16-10-5-12(11-18(16)30-29-19)15-3-1-2-4-17(15)21(25,26)27/h1-11H,(H,28,29) | PDB
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| n/a | n/a | 70 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301868
(6-(3-methylpyridin-2-yl)-N-(4-(trifluoromethyl)phe...)Show SMILES Cc1cccnc1-c1ccc2c(Nc3ccc(cc3)C(F)(F)F)noc2c1 Show InChI InChI=1S/C20H14F3N3O/c1-12-3-2-10-24-18(12)13-4-9-16-17(11-13)27-26-19(16)25-15-7-5-14(6-8-15)20(21,22)23/h2-11H,1H3,(H,25,26) | PDB
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| n/a | n/a | 70 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301863
(7-(trifluoromethyl)-N-(6-(trifluoromethyl)pyridin-...)Show InChI InChI=1S/C14H7F6N3O/c15-13(16,17)9-3-1-2-8-11(9)24-23-12(8)22-7-4-5-10(21-6-7)14(18,19)20/h1-6H,(H,22,23) | PDB
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| n/a | n/a | 74 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301873
(CHEMBL576719 | N-(4-(trifluoromethyl)phenyl)benzo[...)Show InChI InChI=1S/C14H9F3N2O/c15-14(16,17)9-5-7-10(8-6-9)18-13-11-3-1-2-4-12(11)20-19-13/h1-8H,(H,18,19) | PDB
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| n/a | n/a | 76 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301861
(6-(1H-indol-5-yl)-N-(4-(trifluoromethyl)phenyl)ben...)Show SMILES FC(F)(F)c1ccc(Nc2noc3cc(ccc23)-c2ccc3[nH]ccc3c2)cc1 Show InChI InChI=1S/C22H14F3N3O/c23-22(24,25)16-3-5-17(6-4-16)27-21-18-7-1-14(12-20(18)29-28-21)13-2-8-19-15(11-13)9-10-26-19/h1-12,26H,(H,27,28) | PDB
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| n/a | n/a | 77 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301869
(7-(2-(trifluoromethyl)phenyl)-N-(4-(trifluoromethy...)Show SMILES FC(F)(F)c1ccc(Nc2noc3c(cccc23)-c2ccccc2C(F)(F)F)cc1 Show InChI InChI=1S/C21H12F6N2O/c22-20(23,24)12-8-10-13(11-9-12)28-19-16-6-3-5-15(18(16)30-29-19)14-4-1-2-7-17(14)21(25,26)27/h1-11H,(H,28,29) | PDB
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| n/a | n/a | 79 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301865
(6-(2-fluorophenyl)-N-(4-(trifluoromethyl)phenyl)be...)Show SMILES Fc1ccccc1-c1ccc2c(Nc3ccc(cc3)C(F)(F)F)noc2c1 Show InChI InChI=1S/C20H12F4N2O/c21-17-4-2-1-3-15(17)12-5-10-16-18(11-12)27-26-19(16)25-14-8-6-13(7-9-14)20(22,23)24/h1-11H,(H,25,26) | PDB
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| n/a | n/a | 91 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301856
(7-(trifluoromethyl)-N-(4-(trifluoromethyl)phenyl)b...)Show InChI InChI=1S/C15H8F6N2O/c16-14(17,18)8-4-6-9(7-5-8)22-13-10-2-1-3-11(15(19,20)21)12(10)24-23-13/h1-7H,(H,22,23) | PDB
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| n/a | n/a | 127 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301870
(7-(3-(trifluoromethyl)phenyl)-N-(4-(trifluoromethy...)Show SMILES FC(F)(F)c1ccc(Nc2noc3c(cccc23)-c2cccc(c2)C(F)(F)F)cc1 Show InChI InChI=1S/C21H12F6N2O/c22-20(23,24)13-7-9-15(10-8-13)28-19-17-6-2-5-16(18(17)30-29-19)12-3-1-4-14(11-12)21(25,26)27/h1-11H,(H,28,29) | PDB
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| n/a | n/a | 130 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301875
(CHEMBL585011 | N-(3-(trifluoromethoxy)phenyl)benzo...)Show InChI InChI=1S/C14H9F3N2O2/c15-14(16,17)20-10-5-3-4-9(8-10)18-13-11-6-1-2-7-12(11)21-19-13/h1-8H,(H,18,19) | PDB
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| n/a | n/a | 160 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301875
(CHEMBL585011 | N-(3-(trifluoromethoxy)phenyl)benzo...)Show InChI InChI=1S/C14H9F3N2O2/c15-14(16,17)20-10-5-3-4-9(8-10)18-13-11-6-1-2-7-12(11)21-19-13/h1-8H,(H,18,19) | PDB
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| n/a | n/a | 160 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301874
(CHEMBL578048 | N-(4-(trifluoromethoxy)phenyl)benzo...)Show InChI InChI=1S/C14H9F3N2O2/c15-14(16,17)20-10-7-5-9(6-8-10)18-13-11-3-1-2-4-12(11)21-19-13/h1-8H,(H,18,19) | PDB
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| n/a | n/a | 170 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301876
(CHEMBL578782 | N-(biphenyl-4-yl)benzo[d]isoxazol-3...)Show InChI InChI=1S/C19H14N2O/c1-2-6-14(7-3-1)15-10-12-16(13-11-15)20-19-17-8-4-5-9-18(17)22-21-19/h1-13H,(H,20,21) | PDB
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| n/a | n/a | 170 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301868
(6-(3-methylpyridin-2-yl)-N-(4-(trifluoromethyl)phe...)Show SMILES Cc1cccnc1-c1ccc2c(Nc3ccc(cc3)C(F)(F)F)noc2c1 Show InChI InChI=1S/C20H14F3N3O/c1-12-3-2-10-24-18(12)13-4-9-16-17(11-13)27-26-19(16)25-15-7-5-14(6-8-15)20(21,22)23/h2-11H,1H3,(H,25,26) | PDB
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| n/a | n/a | 290 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301872
(7-(trifluoromethyl)-N-(4-(trifluoromethyl)phenyl)i...)Show InChI InChI=1S/C14H7F6N3O/c15-13(16,17)7-1-3-8(4-2-7)22-12-9-5-6-21-11(14(18,19)20)10(9)24-23-12/h1-6H,(H,22,23) | PDB
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| n/a | n/a | 300 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301895
(CHEMBL585010 | N-(4-(trifluoromethyl)phenyl)isoxaz...)Show InChI InChI=1S/C13H8F3N3O/c14-13(15,16)8-1-3-9(4-2-8)18-12-10-7-17-6-5-11(10)20-19-12/h1-7H,(H,18,19) | PDB
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| n/a | n/a | 340 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301864
(6-(3-(trifluoromethyl)phenyl)-N-(4-(trifluoromethy...)Show SMILES FC(F)(F)c1ccc(Nc2noc3cc(ccc23)-c2cccc(c2)C(F)(F)F)cc1 Show InChI InChI=1S/C21H12F6N2O/c22-20(23,24)14-5-7-16(8-6-14)28-19-17-9-4-13(11-18(17)30-29-19)12-2-1-3-15(10-12)21(25,26)27/h1-11H,(H,28,29) | PDB
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| n/a | n/a | 470 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301864
(6-(3-(trifluoromethyl)phenyl)-N-(4-(trifluoromethy...)Show SMILES FC(F)(F)c1ccc(Nc2noc3cc(ccc23)-c2cccc(c2)C(F)(F)F)cc1 Show InChI InChI=1S/C21H12F6N2O/c22-20(23,24)14-5-7-16(8-6-14)28-19-17-9-4-13(11-18(17)30-29-19)12-2-1-3-15(10-12)21(25,26)27/h1-11H,(H,28,29) | PDB
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| n/a | n/a | 570 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301876
(CHEMBL578782 | N-(biphenyl-4-yl)benzo[d]isoxazol-3...)Show InChI InChI=1S/C19H14N2O/c1-2-6-14(7-3-1)15-10-12-16(13-11-15)20-19-17-8-4-5-9-18(17)22-21-19/h1-13H,(H,20,21) | PDB
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| n/a | n/a | 740 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301855
(CHEMBL565960 | N-(naphthalen-1-yl)benzo[d]isoxazol...)Show InChI InChI=1S/C17H12N2O/c1-2-8-13-12(6-1)7-5-10-15(13)18-17-14-9-3-4-11-16(14)20-19-17/h1-11H,(H,18,19) | PDB
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| n/a | n/a | 840 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301853
(CHEMBL565950 | N-(biphenyl-3-yl)benzo[d]isoxazol-3...)Show InChI InChI=1S/C19H14N2O/c1-2-7-14(8-3-1)15-9-6-10-16(13-15)20-19-17-11-4-5-12-18(17)22-21-19/h1-13H,(H,20,21) | PDB
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| n/a | n/a | 960 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301897
(CHEMBL578380 | N-(2-(trifluoromethyl)phenyl)benzo[...)Show InChI InChI=1S/C14H9F3N2O/c15-14(16,17)10-6-2-3-7-11(10)18-13-9-5-1-4-8-12(9)20-19-13/h1-8H,(H,18,19) | PDB
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| n/a | n/a | 960 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301896
(CHEMBL578781 | N-(4-(trifluoromethyl)phenyl)isoxaz...)Show InChI InChI=1S/C13H8F3N3O/c14-13(15,16)8-3-5-9(6-4-8)18-12-11-10(20-19-12)2-1-7-17-11/h1-7H,(H,18,19) | PDB
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| n/a | n/a | 1.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301854
(CHEMBL577471 | N-(naphthalen-2-yl)benzo[d]isoxazol...)Show InChI InChI=1S/C17H12N2O/c1-2-6-13-11-14(10-9-12(13)5-1)18-17-15-7-3-4-8-16(15)20-19-17/h1-11H,(H,18,19) | PDB
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| n/a | n/a | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301889
(CHEMBL572182 | N-(4-(trifluoromethyl)benzyl)benzo[...)Show InChI InChI=1S/C15H11F3N2O/c16-15(17,18)11-7-5-10(6-8-11)9-19-14-12-3-1-2-4-13(12)21-20-14/h1-8H,9H2,(H,19,20) | PDB
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| n/a | n/a | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301856
(7-(trifluoromethyl)-N-(4-(trifluoromethyl)phenyl)b...)Show InChI InChI=1S/C15H8F6N2O/c16-14(17,18)8-4-6-9(7-5-8)22-13-10-2-1-3-11(15(19,20)21)12(10)24-23-13/h1-7H,(H,22,23) | PDB
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| n/a | n/a | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH assessed as DHET production in presence of 10% human serum |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301858
(5-(trifluoromethyl)-N-(4-(trifluoromethyl)phenyl)b...)Show InChI InChI=1S/C15H8F6N2O/c16-14(17,18)8-1-4-10(5-2-8)22-13-11-7-9(15(19,20)21)3-6-12(11)24-23-13/h1-7H,(H,22,23) | PDB
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| n/a | n/a | 1.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301886
(CHEMBL579018 | N-phenyl-5-(trifluoromethyl)-1,3,4-...)Show InChI InChI=1S/C9H6F3N3O/c10-9(11,12)7-14-15-8(16-7)13-6-4-2-1-3-5-6/h1-5H,(H,13,15) | PDB
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| n/a | n/a | 2.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301887
(CHEMBL568223 | N-(4-(trifluoromethyl)phenyl)benzo[...)Show InChI InChI=1S/C14H9F3N2S/c15-14(16,17)9-5-7-10(8-6-9)18-13-11-3-1-2-4-12(11)20-19-13/h1-8H,(H,18,19) | PDB
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| n/a | n/a | 2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301863
(7-(trifluoromethyl)-N-(6-(trifluoromethyl)pyridin-...)Show InChI InChI=1S/C14H7F6N3O/c15-13(16,17)9-3-1-2-8-11(9)24-23-12(8)22-7-4-5-10(21-6-7)14(18,19)20/h1-6H,(H,22,23) | PDB
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| n/a | n/a | 3.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301855
(CHEMBL565960 | N-(naphthalen-1-yl)benzo[d]isoxazol...)Show InChI InChI=1S/C17H12N2O/c1-2-8-13-12(6-1)7-5-10-15(13)18-17-14-9-3-4-11-16(14)20-19-17/h1-11H,(H,18,19) | PDB
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| n/a | n/a | 4.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301878
(5-phenyl-N-(4-(trifluoromethyl)benzyl)isoxazol-3-a...)Show InChI InChI=1S/C17H13F3N2O/c18-17(19,20)14-8-6-12(7-9-14)11-21-16-10-15(23-22-16)13-4-2-1-3-5-13/h1-10H,11H2,(H,21,22) | PDB
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| n/a | n/a | 4.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301898
(CHEMBL578771 | N-(2-(trifluoromethoxy)phenyl)benzo...)Show InChI InChI=1S/C14H9F3N2O2/c15-14(16,17)20-12-8-4-2-6-10(12)18-13-9-5-1-3-7-11(9)21-19-13/h1-8H,(H,18,19) | PDB
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| n/a | n/a | 5.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301891
(CHEMBL576254 | N-benzylbenzo[d]oxazol-2-amine)Show InChI InChI=1S/C14H12N2O/c1-2-6-11(7-3-1)10-15-14-16-12-8-4-5-9-13(12)17-14/h1-9H,10H2,(H,15,16) | PDB
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| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301862
(7-(trifluoromethyl)-N-(5-(trifluoromethyl)pyridin-...)Show InChI InChI=1S/C14H7F6N3O/c15-13(16,17)7-4-5-10(21-6-7)22-12-8-2-1-3-9(14(18,19)20)11(8)24-23-12/h1-6H,(H,21,22,23) | PDB
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| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301885
(5-benzyl-N-phenyl-1,3,4-oxadiazol-2-amine | CHEMBL...)Show InChI InChI=1S/C15H13N3O/c1-3-7-12(8-4-1)11-14-17-18-15(19-14)16-13-9-5-2-6-10-13/h1-10H,11H2,(H,16,18) | PDB
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| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301884
(CHEMBL577043 | N,5-dibenzyl-1,3,4-oxadiazol-2-amin...)Show InChI InChI=1S/C16H15N3O/c1-3-7-13(8-4-1)11-15-18-19-16(20-15)17-12-14-9-5-2-6-10-14/h1-10H,11-12H2,(H,17,19) | PDB
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| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301888
(CHEMBL579041 | N-(4-(trifluoromethyl)phenyl)-1H-in...)Show InChI InChI=1S/C14H10F3N3/c15-14(16,17)9-5-7-10(8-6-9)18-13-11-3-1-2-4-12(11)19-20-13/h1-8H,(H2,18,19,20) | PDB
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| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301882
(6-phenyl-N-(3-(trifluoromethyl)benzyl)pyrimidin-4-...)Show InChI InChI=1S/C18H14F3N3/c19-18(20,21)15-8-4-5-13(9-15)11-22-17-10-16(23-12-24-17)14-6-2-1-3-7-14/h1-10,12H,11H2,(H,22,23,24) | PDB
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| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301883
(CHEMBL568745 | N-benzyl-5-phenyl-1,3,4-oxadiazol-2...)Show InChI InChI=1S/C15H13N3O/c1-3-7-12(8-4-1)11-16-15-18-17-14(19-15)13-9-5-2-6-10-13/h1-10H,11H2,(H,16,18) | PDB
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| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301890
(CHEMBL565734 | N-benzylbenzo[d]thiazol-2-amine)Show InChI InChI=1S/C14H12N2S/c1-2-6-11(7-3-1)10-15-14-16-12-8-4-5-9-13(12)17-14/h1-9H,10H2,(H,15,16) | PDB
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| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301881
(CHEMBL568744 | N-benzyl-5-phenylpyrazin-2-amine)Show InChI InChI=1S/C17H15N3/c1-3-7-14(8-4-1)11-19-17-13-18-16(12-20-17)15-9-5-2-6-10-15/h1-10,12-13H,11H2,(H,19,20) | PDB
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Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Rattus norvegicus) | BDBM50301862
(7-(trifluoromethyl)-N-(5-(trifluoromethyl)pyridin-...)Show InChI InChI=1S/C14H7F6N3O/c15-13(16,17)7-4-5-10(21-6-7)22-12-8-2-1-3-9(14(18,19)20)11(8)24-23-12/h1-6H,(H,21,22,23) | PDB
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| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of rat sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301879
(CHEMBL501669 | N-(5-Phenylpyridin-2-yl)benzylamine...)Show InChI InChI=1S/C18H16N2/c1-3-7-15(8-4-1)13-19-18-12-11-17(14-20-18)16-9-5-2-6-10-16/h1-12,14H,13H2,(H,19,20) | PDB
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| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301892
(CHEMBL584810 | N-benzylquinoxalin-2-amine)Show InChI InChI=1S/C15H13N3/c1-2-6-12(7-3-1)10-17-15-11-16-13-8-4-5-9-14(13)18-15/h1-9,11H,10H2,(H,17,18) | PDB
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Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301877
(5-phenyl-N-(4-(trifluoromethyl)phenyl)isoxazol-3-a...)Show InChI InChI=1S/C16H11F3N2O/c17-16(18,19)12-6-8-13(9-7-12)20-15-10-14(22-21-15)11-4-2-1-3-5-11/h1-10H,(H,20,21) | PDB
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AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
Bifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50301880
(CHEMBL579017 | N-benzyl-4-phenylpyridin-2-amine)Show InChI InChI=1S/C18H16N2/c1-3-7-15(8-4-1)14-20-18-13-17(11-12-19-18)16-9-5-2-6-10-16/h1-13H,14H2,(H,19,20) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of human sEH |
Bioorg Med Chem Lett 19: 5716-21 (2009)
Article DOI: 10.1016/j.bmcl.2009.08.006
BindingDB Entry DOI: 10.7270/Q2Z0388B |
More data for this
Ligand-Target Pair | |
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