Found 9 hits for monomerid = 50295549 Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
EBifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50295549
(4-(3-(pyridin-2-yl)-1,2,4-oxadiazol-5-yl)-N-(4-(tr...)Show SMILES FC(F)(F)c1ccc(NC(=O)N2CCC(CC2)c2nc(no2)-c2ccccn2)cc1 Show InChI InChI=1S/C20H18F3N5O2/c21-20(22,23)14-4-6-15(7-5-14)25-19(29)28-11-8-13(9-12-28)18-26-17(27-30-18)16-3-1-2-10-24-16/h1-7,10,13H,8-9,11-12H2,(H,25,29) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 7 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human sEH |
J Med Chem 52: 5009-12 (2010)
Article DOI: 10.1021/jm900725r BindingDB Entry DOI: 10.7270/Q2TX3G8W |
More data for this Ligand-Target Pair | |
Epoxide hydrolase 2
(Rattus norvegicus) | BDBM50295549
(4-(3-(pyridin-2-yl)-1,2,4-oxadiazol-5-yl)-N-(4-(tr...)Show SMILES FC(F)(F)c1ccc(NC(=O)N2CCC(CC2)c2nc(no2)-c2ccccn2)cc1 Show InChI InChI=1S/C20H18F3N5O2/c21-20(22,23)14-4-6-15(7-5-14)25-19(29)28-11-8-13(9-12-28)18-26-17(27-30-18)16-3-1-2-10-24-16/h1-7,10,13H,8-9,11-12H2,(H,25,29) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 17 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of rat sEH |
J Med Chem 52: 5009-12 (2010)
Article DOI: 10.1021/jm900725r BindingDB Entry DOI: 10.7270/Q2TX3G8W |
More data for this Ligand-Target Pair | |
EBifunctional epoxide hydrolase 2
(Homo sapiens (Human)) | BDBM50295549
(4-(3-(pyridin-2-yl)-1,2,4-oxadiazol-5-yl)-N-(4-(tr...)Show SMILES FC(F)(F)c1ccc(NC(=O)N2CCC(CC2)c2nc(no2)-c2ccccn2)cc1 Show InChI InChI=1S/C20H18F3N5O2/c21-20(22,23)14-4-6-15(7-5-14)25-19(29)28-11-8-13(9-12-28)18-26-17(27-30-18)16-3-1-2-10-24-16/h1-7,10,13H,8-9,11-12H2,(H,25,29) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 7 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human sEH in HEK293 cells assessed as conversion of 14,15-epoxyeicosatrienoic acid to 14,15-dihydroepoxyeicosatrienoic acid |
J Med Chem 52: 5009-12 (2010)
Article DOI: 10.1021/jm900725r BindingDB Entry DOI: 10.7270/Q2TX3G8W |
More data for this Ligand-Target Pair | |
Cytochrome P450 2C9
(Homo sapiens (Human)) | BDBM50295549
(4-(3-(pyridin-2-yl)-1,2,4-oxadiazol-5-yl)-N-(4-(tr...)Show SMILES FC(F)(F)c1ccc(NC(=O)N2CCC(CC2)c2nc(no2)-c2ccccn2)cc1 Show InChI InChI=1S/C20H18F3N5O2/c21-20(22,23)14-4-6-15(7-5-14)25-19(29)28-11-8-13(9-12-28)18-26-17(27-30-18)16-3-1-2-10-24-16/h1-7,10,13H,8-9,11-12H2,(H,25,29) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
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 CYP2C9 |
J Med Chem 52: 5009-12 (2010)
Article DOI: 10.1021/jm900725r BindingDB Entry DOI: 10.7270/Q2TX3G8W |
More data for this Ligand-Target Pair | |
Sodium channel protein type 5 subunit alpha
(Homo sapiens (Human)) | BDBM50295549
(4-(3-(pyridin-2-yl)-1,2,4-oxadiazol-5-yl)-N-(4-(tr...)Show SMILES FC(F)(F)c1ccc(NC(=O)N2CCC(CC2)c2nc(no2)-c2ccccn2)cc1 Show InChI InChI=1S/C20H18F3N5O2/c21-20(22,23)14-4-6-15(7-5-14)25-19(29)28-11-8-13(9-12-28)18-26-17(27-30-18)16-3-1-2-10-24-16/h1-7,10,13H,8-9,11-12H2,(H,25,29) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
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 Nav1.5 channel |
J Med Chem 52: 5009-12 (2010)
Article DOI: 10.1021/jm900725r BindingDB Entry DOI: 10.7270/Q2TX3G8W |
More data for this Ligand-Target Pair | |
Cytochrome P450 3A4
(Homo sapiens (Human)) | BDBM50295549
(4-(3-(pyridin-2-yl)-1,2,4-oxadiazol-5-yl)-N-(4-(tr...)Show SMILES FC(F)(F)c1ccc(NC(=O)N2CCC(CC2)c2nc(no2)-c2ccccn2)cc1 Show InChI InChI=1S/C20H18F3N5O2/c21-20(22,23)14-4-6-15(7-5-14)25-19(29)28-11-8-13(9-12-28)18-26-17(27-30-18)16-3-1-2-10-24-16/h1-7,10,13H,8-9,11-12H2,(H,25,29) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
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 CYP3A4 |
J Med Chem 52: 5009-12 (2010)
Article DOI: 10.1021/jm900725r BindingDB Entry DOI: 10.7270/Q2TX3G8W |
More data for this Ligand-Target Pair | |
Calcium channel (Type L)
(Homo sapiens (Human)) | BDBM50295549
(4-(3-(pyridin-2-yl)-1,2,4-oxadiazol-5-yl)-N-(4-(tr...)Show SMILES FC(F)(F)c1ccc(NC(=O)N2CCC(CC2)c2nc(no2)-c2ccccn2)cc1 Show InChI InChI=1S/C20H18F3N5O2/c21-20(22,23)14-4-6-15(7-5-14)25-19(29)28-11-8-13(9-12-28)18-26-17(27-30-18)16-3-1-2-10-24-16/h1-7,10,13H,8-9,11-12H2,(H,25,29) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of Cav 1.2 channel |
J Med Chem 52: 5009-12 (2010)
Article DOI: 10.1021/jm900725r BindingDB Entry DOI: 10.7270/Q2TX3G8W |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50295549
(4-(3-(pyridin-2-yl)-1,2,4-oxadiazol-5-yl)-N-(4-(tr...)Show SMILES FC(F)(F)c1ccc(NC(=O)N2CCC(CC2)c2nc(no2)-c2ccccn2)cc1 Show InChI InChI=1S/C20H18F3N5O2/c21-20(22,23)14-4-6-15(7-5-14)25-19(29)28-11-8-13(9-12-28)18-26-17(27-30-18)16-3-1-2-10-24-16/h1-7,10,13H,8-9,11-12H2,(H,25,29) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 8.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of IKr channel |
J Med Chem 52: 5009-12 (2010)
Article DOI: 10.1021/jm900725r BindingDB Entry DOI: 10.7270/Q2TX3G8W |
More data for this Ligand-Target Pair | |
Cytochrome P450 2D6
(Homo sapiens (Human)) | BDBM50295549
(4-(3-(pyridin-2-yl)-1,2,4-oxadiazol-5-yl)-N-(4-(tr...)Show SMILES FC(F)(F)c1ccc(NC(=O)N2CCC(CC2)c2nc(no2)-c2ccccn2)cc1 Show InChI InChI=1S/C20H18F3N5O2/c21-20(22,23)14-4-6-15(7-5-14)25-19(29)28-11-8-13(9-12-28)18-26-17(27-30-18)16-3-1-2-10-24-16/h1-7,10,13H,8-9,11-12H2,(H,25,29) | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
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 CYP2D6 |
J Med Chem 52: 5009-12 (2010)
Article DOI: 10.1021/jm900725r BindingDB Entry DOI: 10.7270/Q2TX3G8W |
More data for this Ligand-Target Pair | |