Compile Data Set for Download or QSAR

Found 3 hits Enz. Inhib. hit(s) with Target = 'Bifunctional epoxide hydrolase 2' and Ligand = 'BDBM50268320'   

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))	BDBM50268320 ((+/-)-6-fluoro-N-((trans)-2-phenylcyclopropyl)spir...) Show SMILES Fc1ccc2OC3(CCN(CC3)C(=O)N[C@H]3C[C@@H]3c3ccccc3)CCc2c1 |r| Show InChI InChI=1S/C23H25FN2O2/c24-18-6-7-21-17(14-18)8-9-23(28-21)10-12-26(13-11-23)22(27)25-20-15-19(20)16-4-2-1-3-5-16/h1-7,14,19-20H,8-13,15H2,(H,25,27)/t19-,20+/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	<1	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibition of human soluble epoxide hydrolase				Bioorg Med Chem Lett 19: 3398-404 (2009) Article DOI: 10.1016/j.bmcl.2009.05.036 BindingDB Entry DOI: 10.7270/Q20C4VP7
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50268320 ((+/-)-6-fluoro-N-((trans)-2-phenylcyclopropyl)spir...) Show SMILES Fc1ccc2OC3(CCN(CC3)C(=O)N[C@H]3C[C@@H]3c3ccccc3)CCc2c1 |r| Show InChI InChI=1S/C23H25FN2O2/c24-18-6-7-21-17(14-18)8-9-23(28-21)10-12-26(13-11-23)22(27)25-20-15-19(20)16-4-2-1-3-5-16/h1-7,14,19-20H,8-13,15H2,(H,25,27)/t19-,20+/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibition of human soluble epoxide hydrolase				Bioorg Med Chem Lett 19: 3398-404 (2009) Article DOI: 10.1016/j.bmcl.2009.05.036 BindingDB Entry DOI: 10.7270/Q20C4VP7
					More data for this Ligand-Target Pair
Bifunctional epoxide hydrolase 2 (Rattus norvegicus)	BDBM50268320 ((+/-)-6-fluoro-N-((trans)-2-phenylcyclopropyl)spir...) Show SMILES Fc1ccc2OC3(CCN(CC3)C(=O)N[C@H]3C[C@@H]3c3ccccc3)CCc2c1 |r| Show InChI InChI=1S/C23H25FN2O2/c24-18-6-7-21-17(14-18)8-9-23(28-21)10-12-26(13-11-23)22(27)25-20-15-19(20)16-4-2-1-3-5-16/h1-7,14,19-20H,8-13,15H2,(H,25,27)/t19-,20+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	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 rat soluble epoxide hydrolase				Bioorg Med Chem Lett 19: 3398-404 (2009) Article DOI: 10.1016/j.bmcl.2009.05.036 BindingDB Entry DOI: 10.7270/Q20C4VP7
					More data for this Ligand-Target Pair