BDBM50204523 1-(5-(4-aminopyridin-2-yl)oxazol-2-yl)-7-phenylheptan-1-one::CHEMBL220686

SMILES: Nc1ccnc(c1)-c1cnc(o1)C(=O)CCCCCCc1ccccc1

InChI Key: InChIKey=BJJKIYZDDJWPTF-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 = 50204523   

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))	BDBM50204523 (1-(5-(4-aminopyridin-2-yl)oxazol-2-yl)-7-phenylhep...) Show SMILES Nc1ccnc(c1)-c1cnc(o1)C(=O)CCCCCCc1ccccc1 Show InChI InChI=1S/C21H23N3O2/c22-17-12-13-23-18(14-17)20-15-24-21(26-20)19(25)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,(H2,22,23)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	25	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))	BDBM50204523 (1-(5-(4-aminopyridin-2-yl)oxazol-2-yl)-7-phenylhep...) Show SMILES Nc1ccnc(c1)-c1cnc(o1)C(=O)CCCCCCc1ccccc1 Show InChI InChI=1S/C21H23N3O2/c22-17-12-13-23-18(14-17)20-15-24-21(26-20)19(25)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,(H2,22,23)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	340	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
Neutral cholesterol ester hydrolase 1 (Homo sapiens (Human))	BDBM50204523 (1-(5-(4-aminopyridin-2-yl)oxazol-2-yl)-7-phenylhep...) Show SMILES Nc1ccnc(c1)-c1cnc(o1)C(=O)CCCCCCc1ccccc1 Show InChI InChI=1S/C21H23N3O2/c22-17-12-13-23-18(14-17)20-15-24-21(26-20)19(25)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,(H2,22,23)	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
Acyl-CoA: cholesterol acyltransferase (ACAT) (Homo sapiens (Human))	BDBM50204523 (1-(5-(4-aminopyridin-2-yl)oxazol-2-yl)-7-phenylhep...) Show SMILES Nc1ccnc(c1)-c1cnc(o1)C(=O)CCCCCCc1ccccc1 Show InChI InChI=1S/C21H23N3O2/c22-17-12-13-23-18(14-17)20-15-24-21(26-20)19(25)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,(H2,22,23)	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.40E+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