BDBM50204527 6-(2-(7-phenylheptanoyl)oxazol-5-yl)pyrimidine-2,4(1H,3H)-dione::CHEMBL220687

SMILES: O=C(CCCCCCc1ccccc1)c1ncc(o1)-c1cc(=O)[nH]c(=O)[nH]1

InChI Key: InChIKey=MCKAMZSBTSLCAF-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 = 50204527   

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))	BDBM50204527 (6-(2-(7-phenylheptanoyl)oxazol-5-yl)pyrimidine-2,4...) Show SMILES O=C(CCCCCCc1ccccc1)c1ncc(o1)-c1cc(=O)[nH]c(=O)[nH]1 Show InChI InChI=1S/C20H21N3O4/c24-16(11-7-2-1-4-8-14-9-5-3-6-10-14)19-21-13-17(27-19)15-12-18(25)23-20(26)22-15/h3,5-6,9-10,12-13H,1-2,4,7-8,11H2,(H2,22,23,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	12	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))	BDBM50204527 (6-(2-(7-phenylheptanoyl)oxazol-5-yl)pyrimidine-2,4...) Show SMILES O=C(CCCCCCc1ccccc1)c1ncc(o1)-c1cc(=O)[nH]c(=O)[nH]1 Show InChI InChI=1S/C20H21N3O4/c24-16(11-7-2-1-4-8-14-9-5-3-6-10-14)19-21-13-17(27-19)15-12-18(25)23-20(26)22-15/h3,5-6,9-10,12-13H,1-2,4,7-8,11H2,(H2,22,23,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	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))	BDBM50204527 (6-(2-(7-phenylheptanoyl)oxazol-5-yl)pyrimidine-2,4...) Show SMILES O=C(CCCCCCc1ccccc1)c1ncc(o1)-c1cc(=O)[nH]c(=O)[nH]1 Show InChI InChI=1S/C20H21N3O4/c24-16(11-7-2-1-4-8-14-9-5-3-6-10-14)19-21-13-17(27-19)15-12-18(25)23-20(26)22-15/h3,5-6,9-10,12-13H,1-2,4,7-8,11H2,(H2,22,23,25,26)	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.00E+4	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))	BDBM50204527 (6-(2-(7-phenylheptanoyl)oxazol-5-yl)pyrimidine-2,4...) Show SMILES O=C(CCCCCCc1ccccc1)c1ncc(o1)-c1cc(=O)[nH]c(=O)[nH]1 Show InChI InChI=1S/C20H21N3O4/c24-16(11-7-2-1-4-8-14-9-5-3-6-10-14)19-21-13-17(27-19)15-12-18(25)23-20(26)22-15/h3,5-6,9-10,12-13H,1-2,4,7-8,11H2,(H2,22,23,25,26)	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