BDBM50204524 7-phenyl-1-(5-(piperidine-1-carbonyl)oxazol-2-yl)heptan-1-one::CHEMBL376417

SMILES: O=C(CCCCCCc1ccccc1)c1ncc(o1)C(=O)N1CCCCC1

InChI Key: InChIKey=FZYNDZPFUPHGRM-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 = 50204524   

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))	BDBM50204524 (7-phenyl-1-(5-(piperidine-1-carbonyl)oxazol-2-yl)h...) Show SMILES O=C(CCCCCCc1ccccc1)c1ncc(o1)C(=O)N1CCCCC1 Show InChI InChI=1S/C22H28N2O3/c25-19(14-8-2-1-5-11-18-12-6-3-7-13-18)21-23-17-20(27-21)22(26)24-15-9-4-10-16-24/h3,6-7,12-13,17H,1-2,4-5,8-11,14-16H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	8	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))	BDBM50204524 (7-phenyl-1-(5-(piperidine-1-carbonyl)oxazol-2-yl)h...) Show SMILES O=C(CCCCCCc1ccccc1)c1ncc(o1)C(=O)N1CCCCC1 Show InChI InChI=1S/C22H28N2O3/c25-19(14-8-2-1-5-11-18-12-6-3-7-13-18)21-23-17-20(27-21)22(26)24-15-9-4-10-16-24/h3,6-7,12-13,17H,1-2,4-5,8-11,14-16H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	450	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))	BDBM50204524 (7-phenyl-1-(5-(piperidine-1-carbonyl)oxazol-2-yl)h...) Show SMILES O=C(CCCCCCc1ccccc1)c1ncc(o1)C(=O)N1CCCCC1 Show InChI InChI=1S/C22H28N2O3/c25-19(14-8-2-1-5-11-18-12-6-3-7-13-18)21-23-17-20(27-21)22(26)24-15-9-4-10-16-24/h3,6-7,12-13,17H,1-2,4-5,8-11,14-16H2	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	8.00E+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))	BDBM50204524 (7-phenyl-1-(5-(piperidine-1-carbonyl)oxazol-2-yl)h...) Show SMILES O=C(CCCCCCc1ccccc1)c1ncc(o1)C(=O)N1CCCCC1 Show InChI InChI=1S/C22H28N2O3/c25-19(14-8-2-1-5-11-18-12-6-3-7-13-18)21-23-17-20(27-21)22(26)24-15-9-4-10-16-24/h3,6-7,12-13,17H,1-2,4-5,8-11,14-16H2	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