BDBM50454628 CHEMBL4217146

SMILES: OC(=O)c1ccc(O[C@H]2CC[C@@H](CC2)NC(=O)NC2CCCCC2)cc1

InChI Key: InChIKey=OVKYOOTTWMYNIV-SAABIXHNSA-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 = 50454628   

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
Fatty-acid amide hydrolase 1 (Homo sapiens (Human))	BDBM50454628 (CHEMBL4217146) Show SMILES OC(=O)c1ccc(O[C@H]2CC[C@@H](CC2)NC(=O)NC2CCCCC2)cc1 |r,wU:8.7,wD:11.14,(23.43,-6.87,;22.09,-7.64,;22.09,-9.18,;20.75,-6.87,;19.41,-7.63,;18.08,-6.86,;18.09,-5.32,;16.77,-4.55,;15.43,-5.32,;15.42,-6.86,;14.09,-7.62,;12.76,-6.85,;12.75,-5.31,;14.09,-4.54,;11.43,-7.62,;10.09,-6.85,;10.09,-5.31,;8.76,-7.62,;7.42,-6.86,;7.43,-5.32,;6.11,-4.55,;4.77,-5.32,;4.77,-6.86,;6.1,-7.63,;19.42,-4.55,;20.75,-5.32,)| Show InChI InChI=1S/C20H28N2O4/c23-19(24)14-6-10-17(11-7-14)26-18-12-8-16(9-13-18)22-20(25)21-15-4-2-1-3-5-15/h6-7,10-11,15-16,18H,1-5,8-9,12-13H2,(H,23,24)(H2,21,22,25)/t16-,18-	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	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
University of California Davis Curated by ChEMBL					Assay Description Inhibition of human FAAH expressed in baculovirus-infected High Five cells S9 fraction using OMP substrate by fluorescence based assay				Bioorg Med Chem Lett 28: 762-768 (2018) Article DOI: 10.1016/j.bmcl.2018.01.003 BindingDB Entry DOI: 10.7270/Q2PV6NZ4
					More data for this Ligand-Target Pair
EBifunctional epoxide hydrolase 2 (Homo sapiens (Human))	BDBM50454628 (CHEMBL4217146) Show SMILES OC(=O)c1ccc(O[C@H]2CC[C@@H](CC2)NC(=O)NC2CCCCC2)cc1 |r,wU:8.7,wD:11.14,(23.43,-6.87,;22.09,-7.64,;22.09,-9.18,;20.75,-6.87,;19.41,-7.63,;18.08,-6.86,;18.09,-5.32,;16.77,-4.55,;15.43,-5.32,;15.42,-6.86,;14.09,-7.62,;12.76,-6.85,;12.75,-5.31,;14.09,-4.54,;11.43,-7.62,;10.09,-6.85,;10.09,-5.31,;8.76,-7.62,;7.42,-6.86,;7.43,-5.32,;6.11,-4.55,;4.77,-5.32,;4.77,-6.86,;6.1,-7.63,;19.42,-4.55,;20.75,-5.32,)| Show InChI InChI=1S/C20H28N2O4/c23-19(24)14-6-10-17(11-7-14)26-18-12-8-16(9-13-18)22-20(25)21-15-4-2-1-3-5-15/h6-7,10-11,15-16,18H,1-5,8-9,12-13H2,(H,23,24)(H2,21,22,25)/t16-,18-	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6	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 expressed in baculovirus-infected High Five cells S9 fraction using CMNPC substrate by fluo...				Bioorg Med Chem Lett 28: 762-768 (2018) Article DOI: 10.1016/j.bmcl.2018.01.003 BindingDB Entry DOI: 10.7270/Q2PV6NZ4
					More data for this Ligand-Target Pair