BDBM50204479 3-(2-(7-phenylheptanoyl)oxazol-5-yl)benzamide::CHEMBL223406

SMILES: NC(=O)c1cccc(c1)-c1cnc(o1)C(=O)CCCCCCc1ccccc1

InChI Key: InChIKey=UDCOFTGPNZNXSW-UHFFFAOYSA-N

Data: 2 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 5 hits for monomerid = 50204479   

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))	BDBM50204479 (3-(2-(7-phenylheptanoyl)oxazol-5-yl)benzamide | CH...) Show SMILES NC(=O)c1cccc(c1)-c1cnc(o1)C(=O)CCCCCCc1ccccc1 Show InChI InChI=1S/C23H24N2O3/c24-22(27)19-13-8-12-18(15-19)21-16-25-23(28-21)20(26)14-7-2-1-4-9-17-10-5-3-6-11-17/h3,5-6,8,10-13,15-16H,1-2,4,7,9,14H2,(H2,24,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of FAAH				J Med Chem 51: 7327-43 (2009) Article DOI: 10.1021/jm800311k BindingDB Entry DOI: 10.7270/Q2J67HT8
					More data for this Ligand-Target Pair
Fatty-acid amide hydrolase 1 (Homo sapiens (Human))	BDBM50204479 (3-(2-(7-phenylheptanoyl)oxazol-5-yl)benzamide | CH...) Show SMILES NC(=O)c1cccc(c1)-c1cnc(o1)C(=O)CCCCCCc1ccccc1 Show InChI InChI=1S/C23H24N2O3/c24-22(27)19-13-8-12-18(15-19)21-16-25-23(28-21)20(26)14-7-2-1-4-9-17-10-5-3-6-11-17/h3,5-6,8,10-13,15-16H,1-2,4,7,9,14H2,(H2,24,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	6	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))	BDBM50204479 (3-(2-(7-phenylheptanoyl)oxazol-5-yl)benzamide | CH...) Show SMILES NC(=O)c1cccc(c1)-c1cnc(o1)C(=O)CCCCCCc1ccccc1 Show InChI InChI=1S/C23H24N2O3/c24-22(27)19-13-8-12-18(15-19)21-16-25-23(28-21)20(26)14-7-2-1-4-9-17-10-5-3-6-11-17/h3,5-6,8,10-13,15-16H,1-2,4,7,9,14H2,(H2,24,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.70E+3	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))	BDBM50204479 (3-(2-(7-phenylheptanoyl)oxazol-5-yl)benzamide | CH...) Show SMILES NC(=O)c1cccc(c1)-c1cnc(o1)C(=O)CCCCCCc1ccccc1 Show InChI InChI=1S/C23H24N2O3/c24-22(27)19-13-8-12-18(15-19)21-16-25-23(28-21)20(26)14-7-2-1-4-9-17-10-5-3-6-11-17/h3,5-6,8,10-13,15-16H,1-2,4,7,9,14H2,(H2,24,27)	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 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))	BDBM50204479 (3-(2-(7-phenylheptanoyl)oxazol-5-yl)benzamide | CH...) Show SMILES NC(=O)c1cccc(c1)-c1cnc(o1)C(=O)CCCCCCc1ccccc1 Show InChI InChI=1S/C23H24N2O3/c24-22(27)19-13-8-12-18(15-19)21-16-25-23(28-21)20(26)14-7-2-1-4-9-17-10-5-3-6-11-17/h3,5-6,8,10-13,15-16H,1-2,4,7,9,14H2,(H2,24,27)	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