Found 9 hits for monomerid = 50295546 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)) | BDBM50295546
![PNG](/data/jpeg/tenK5029/BindingDB_50295546.png) (CHEMBL551517 | N-(2-phenylcyclopropyl)-4-(3-(pyrim...)Show SMILES O=C(NC1CC1c1ccccc1)N1CCC(CC1)c1nc(no1)-c1ncccn1 Show InChI InChI=1S/C21H22N6O2/c28-21(24-17-13-16(17)14-5-2-1-3-6-14)27-11-7-15(8-12-27)20-25-19(26-29-20)18-22-9-4-10-23-18/h1-6,9-10,15-17H,7-8,11-13H2,(H,24,28) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 33 | 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) | BDBM50295546
![PNG](/data/jpeg/tenK5029/BindingDB_50295546.png) (CHEMBL551517 | N-(2-phenylcyclopropyl)-4-(3-(pyrim...)Show SMILES O=C(NC1CC1c1ccccc1)N1CCC(CC1)c1nc(no1)-c1ncccn1 Show InChI InChI=1S/C21H22N6O2/c28-21(24-17-13-16(17)14-5-2-1-3-6-14)27-11-7-15(8-12-27)20-25-19(26-29-20)18-22-9-4-10-23-18/h1-6,9-10,15-17H,7-8,11-13H2,(H,24,28) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 35 | 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)) | BDBM50295546
![PNG](/data/jpeg/tenK5029/BindingDB_50295546.png) (CHEMBL551517 | N-(2-phenylcyclopropyl)-4-(3-(pyrim...)Show SMILES O=C(NC1CC1c1ccccc1)N1CCC(CC1)c1nc(no1)-c1ncccn1 Show InChI InChI=1S/C21H22N6O2/c28-21(24-17-13-16(17)14-5-2-1-3-6-14)27-11-7-15(8-12-27)20-25-19(26-29-20)18-22-9-4-10-23-18/h1-6,9-10,15-17H,7-8,11-13H2,(H,24,28) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 187 | 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 | |
Epoxide hydrolase 1
(Homo sapiens (Human)) | BDBM50295546
![PNG](/data/jpeg/tenK5029/BindingDB_50295546.png) (CHEMBL551517 | N-(2-phenylcyclopropyl)-4-(3-(pyrim...)Show SMILES O=C(NC1CC1c1ccccc1)N1CCC(CC1)c1nc(no1)-c1ncccn1 Show InChI InChI=1S/C21H22N6O2/c28-21(24-17-13-16(17)14-5-2-1-3-6-14)27-11-7-15(8-12-27)20-25-19(26-29-20)18-22-9-4-10-23-18/h1-6,9-10,15-17H,7-8,11-13H2,(H,24,28) | KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human mEH |
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)) | BDBM50295546
![PNG](/data/jpeg/tenK5029/BindingDB_50295546.png) (CHEMBL551517 | N-(2-phenylcyclopropyl)-4-(3-(pyrim...)Show SMILES O=C(NC1CC1c1ccccc1)N1CCC(CC1)c1nc(no1)-c1ncccn1 Show InChI InChI=1S/C21H22N6O2/c28-21(24-17-13-16(17)14-5-2-1-3-6-14)27-11-7-15(8-12-27)20-25-19(26-29-20)18-22-9-4-10-23-18/h1-6,9-10,15-17H,7-8,11-13H2,(H,24,28) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| 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)) | BDBM50295546
![PNG](/data/jpeg/tenK5029/BindingDB_50295546.png) (CHEMBL551517 | N-(2-phenylcyclopropyl)-4-(3-(pyrim...)Show SMILES O=C(NC1CC1c1ccccc1)N1CCC(CC1)c1nc(no1)-c1ncccn1 Show InChI InChI=1S/C21H22N6O2/c28-21(24-17-13-16(17)14-5-2-1-3-6-14)27-11-7-15(8-12-27)20-25-19(26-29-20)18-22-9-4-10-23-18/h1-6,9-10,15-17H,7-8,11-13H2,(H,24,28) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| 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)) | BDBM50295546
![PNG](/data/jpeg/tenK5029/BindingDB_50295546.png) (CHEMBL551517 | N-(2-phenylcyclopropyl)-4-(3-(pyrim...)Show SMILES O=C(NC1CC1c1ccccc1)N1CCC(CC1)c1nc(no1)-c1ncccn1 Show InChI InChI=1S/C21H22N6O2/c28-21(24-17-13-16(17)14-5-2-1-3-6-14)27-11-7-15(8-12-27)20-25-19(26-29-20)18-22-9-4-10-23-18/h1-6,9-10,15-17H,7-8,11-13H2,(H,24,28) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >3.00E+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)) | BDBM50295546
![PNG](/data/jpeg/tenK5029/BindingDB_50295546.png) (CHEMBL551517 | N-(2-phenylcyclopropyl)-4-(3-(pyrim...)Show SMILES O=C(NC1CC1c1ccccc1)N1CCC(CC1)c1nc(no1)-c1ncccn1 Show InChI InChI=1S/C21H22N6O2/c28-21(24-17-13-16(17)14-5-2-1-3-6-14)27-11-7-15(8-12-27)20-25-19(26-29-20)18-22-9-4-10-23-18/h1-6,9-10,15-17H,7-8,11-13H2,(H,24,28) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >3.00E+4 | 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)) | BDBM50295546
![PNG](/data/jpeg/tenK5029/BindingDB_50295546.png) (CHEMBL551517 | N-(2-phenylcyclopropyl)-4-(3-(pyrim...)Show SMILES O=C(NC1CC1c1ccccc1)N1CCC(CC1)c1nc(no1)-c1ncccn1 Show InChI InChI=1S/C21H22N6O2/c28-21(24-17-13-16(17)14-5-2-1-3-6-14)27-11-7-15(8-12-27)20-25-19(26-29-20)18-22-9-4-10-23-18/h1-6,9-10,15-17H,7-8,11-13H2,(H,24,28) | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| 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 | |