BDBM50204522 7-phenyl-1-(5-(4-(trifluoromethyl)pyridin-2-yl)oxazol-2-yl)heptan-1-one::CHEMBL220556

SMILES: FC(F)(F)c1ccnc(c1)-c1cnc(o1)C(=O)CCCCCCc1ccccc1

InChI Key: InChIKey=WSTXCZKZJBJXQK-UHFFFAOYSA-N

Data: 1 KI  3 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 4 hits for monomerid = 50204522   

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))	BDBM50204522 (7-phenyl-1-(5-(4-(trifluoromethyl)pyridin-2-yl)oxa...) Show SMILES FC(F)(F)c1ccnc(c1)-c1cnc(o1)C(=O)CCCCCCc1ccccc1 Show InChI InChI=1S/C22H21F3N2O2/c23-22(24,25)17-12-13-26-18(14-17)20-15-27-21(29-20)19(28)11-7-2-1-4-8-16-9-5-3-6-10-16/h3,5-6,9-10,12-15H,1-2,4,7-8,11H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	3.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Scripps Research Institute Curated by ChEMBL					Assay Description Inhibition of rat recombinant FAAH expressed in Escherichia coli by [14C]oleamide breakdown				J Med Chem 50: 1058-68 (2007) Article DOI: 10.1021/jm0611509 BindingDB Entry DOI: 10.7270/Q26H4J6G
					More data for this Ligand-Target Pair
Fatty-acid amide hydrolase 1 (Homo sapiens (Human))	BDBM50204522 (7-phenyl-1-(5-(4-(trifluoromethyl)pyridin-2-yl)oxa...) Show SMILES FC(F)(F)c1ccnc(c1)-c1cnc(o1)C(=O)CCCCCCc1ccccc1 Show InChI InChI=1S/C22H21F3N2O2/c23-22(24,25)17-12-13-26-18(14-17)20-15-27-21(29-20)19(28)11-7-2-1-4-8-16-9-5-3-6-10-16/h3,5-6,9-10,12-15H,1-2,4,7-8,11H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.5	n/a	n/a	n/a	n/a	n/a	n/a
The Scripps Research Institute Curated by ChEMBL					Assay Description Inhibition of rat recombinant FAAH expressed in Escherichia coli by [14C]oleamide breakdown				J Med Chem 50: 1058-68 (2007) Article DOI: 10.1021/jm0611509 BindingDB Entry DOI: 10.7270/Q26H4J6G
					More data for this Ligand-Target Pair
Acyl-CoA: cholesterol acyltransferase (ACAT) (Homo sapiens (Human))	BDBM50204522 (7-phenyl-1-(5-(4-(trifluoromethyl)pyridin-2-yl)oxa...) Show SMILES FC(F)(F)c1ccnc(c1)-c1cnc(o1)C(=O)CCCCCCc1ccccc1 Show InChI InChI=1S/C22H21F3N2O2/c23-22(24,25)17-12-13-26-18(14-17)20-15-27-21(29-20)19(28)11-7-2-1-4-8-16-9-5-3-6-10-16/h3,5-6,9-10,12-15H,1-2,4,7-8,11H2	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
The Scripps Research Institute Curated by ChEMBL					Assay Description Inhibition of TGH				J Med Chem 50: 1058-68 (2007) Article DOI: 10.1021/jm0611509 BindingDB Entry DOI: 10.7270/Q26H4J6G
					More data for this Ligand-Target Pair
Neutral cholesterol ester hydrolase 1 (Homo sapiens (Human))	BDBM50204522 (7-phenyl-1-(5-(4-(trifluoromethyl)pyridin-2-yl)oxa...) Show SMILES FC(F)(F)c1ccnc(c1)-c1cnc(o1)C(=O)CCCCCCc1ccccc1 Show InChI InChI=1S/C22H21F3N2O2/c23-22(24,25)17-12-13-26-18(14-17)20-15-27-21(29-20)19(28)11-7-2-1-4-8-16-9-5-3-6-10-16/h3,5-6,9-10,12-15H,1-2,4,7-8,11H2	KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
The Scripps Research Institute Curated by ChEMBL					Assay Description Inhibition of KIAA1363				J Med Chem 50: 1058-68 (2007) Article DOI: 10.1021/jm0611509 BindingDB Entry DOI: 10.7270/Q26H4J6G
					More data for this Ligand-Target Pair