BDBM50217445 CHEMBL397669::cis-1-adamantan-1-yl-3-(4-methoxycyclohexyl)urea

SMILES: O=C(N[C@H]1CC[C@@H](CC1)OCC1CCCCC1)NC12CC3CC(CC(C3)C1)C2

InChI Key: InChIKey=IWFDYFIMYQSEQD-OPPLEYLWSA-N

Data: 2 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50217445   

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))	BDBM50217445 (CHEMBL397669 | cis-1-adamantan-1-yl-3-(4-methoxycy...) Show SMILES O=C(N[C@H]1CC[C@@H](CC1)OCC1CCCCC1)NC12CC3CC(CC(C3)C1)C2 |wU:6.9,wD:3.2,TLB:17:18:21.20.25:23,THB:19:20:23:27.18.26,19:18:21.20.25:23,26:18:21:25.24.23,26:24:21:27.19.18,17:18:21:25.24.23,(-5.73,-20.09,;-4.9,-21.4,;-3.36,-21.34,;-2.65,-19.97,;-1.1,-19.92,;-.39,-18.56,;-1.2,-17.26,;-2.74,-17.31,;-3.47,-18.68,;-.48,-15.9,;1.06,-15.84,;1.78,-14.48,;3.32,-14.43,;4.04,-13.07,;3.23,-11.76,;1.69,-11.82,;.96,-13.18,;-5.62,-22.76,;-7.16,-22.82,;-8.17,-24.1,;-9.58,-23.54,;-11.08,-23.96,;-9.88,-22.68,;-9.89,-21.19,;-8.54,-20.72,;-9.59,-21.95,;-7.15,-21.29,;-8.56,-23.17,)| Show InChI InChI=1S/C24H40N2O2/c27-23(26-24-13-18-10-19(14-24)12-20(11-18)15-24)25-21-6-8-22(9-7-21)28-16-17-4-2-1-3-5-17/h17-22H,1-16H2,(H2,25,26,27)/t18?,19?,20?,21-,22-,24?	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.80	n/a	n/a	n/a	n/a	n/a	n/a
Colorado State University Curated by ChEMBL					Assay Description Inhibition of human recombinant soluble epoxide hydrolase using CMNPC as substrate assessed as appearance of 6-methoxy-2-naphthaldehyde after 10 mins...				Bioorg Med Chem 20: 3255-62 (2012) Article DOI: 10.1016/j.bmc.2012.03.058 BindingDB Entry DOI: 10.7270/Q28W3FB2
					More data for this Ligand-Target Pair
EBifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50217445 (CHEMBL397669 | cis-1-adamantan-1-yl-3-(4-methoxycy...) Show SMILES O=C(N[C@H]1CC[C@@H](CC1)OCC1CCCCC1)NC12CC3CC(CC(C3)C1)C2 |wU:6.9,wD:3.2,TLB:17:18:21.20.25:23,THB:19:20:23:27.18.26,19:18:21.20.25:23,26:18:21:25.24.23,26:24:21:27.19.18,17:18:21:25.24.23,(-5.73,-20.09,;-4.9,-21.4,;-3.36,-21.34,;-2.65,-19.97,;-1.1,-19.92,;-.39,-18.56,;-1.2,-17.26,;-2.74,-17.31,;-3.47,-18.68,;-.48,-15.9,;1.06,-15.84,;1.78,-14.48,;3.32,-14.43,;4.04,-13.07,;3.23,-11.76,;1.69,-11.82,;.96,-13.18,;-5.62,-22.76,;-7.16,-22.82,;-8.17,-24.1,;-9.58,-23.54,;-11.08,-23.96,;-9.88,-22.68,;-9.89,-21.19,;-8.54,-20.72,;-9.59,-21.95,;-7.15,-21.29,;-8.56,-23.17,)| Show InChI InChI=1S/C24H40N2O2/c27-23(26-24-13-18-10-19(14-24)12-20(11-18)15-24)25-21-6-8-22(9-7-21)28-16-17-4-2-1-3-5-17/h17-22H,1-16H2,(H2,25,26,27)/t18?,19?,20?,21-,22-,24?	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
University of California-Davis Curated by ChEMBL					Assay Description Inhibition of human recombinant soluble epoxide hydrolase				J Med Chem 50: 3825-40 (2007) Article DOI: 10.1021/jm070270t BindingDB Entry DOI: 10.7270/Q2TQ62BW
					More data for this Ligand-Target Pair