BDBM50222866 6-(4-chlorophenyl)-3-[(1-isopropylpiperidin-3-yl)methyl]-quinazolin-4(3H)-one::CHEMBL245128

SMILES: CC(C)N1CCC[C@H](Cn2cnc3ccc(cc3c2=O)-c2ccc(Cl)cc2)C1

InChI Key: InChIKey=RFABPDMYZRHJJM-KRWDZBQOSA-N

Data: 2 KI  1 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 3 hits for monomerid = 50222866   

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
Ghrelin receptor (Ovis aries)	BDBM50222866 (6-(4-chlorophenyl)-3-[(1-isopropylpiperidin-3-yl)m...) Show SMILES CC(C)N1CCC[C@H](Cn2cnc3ccc(cc3c2=O)-c2ccc(Cl)cc2)C1 Show InChI InChI=1S/C23H26ClN3O/c1-16(2)26-11-3-4-17(13-26)14-27-15-25-22-10-7-19(12-21(22)23(27)28)18-5-8-20(24)9-6-18/h5-10,12,15-17H,3-4,11,13-14H2,1-2H3/t17-/m0/s1	PDB KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	440	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Bayer Pharmaceuticals Corporation Curated by ChEMBL					Assay Description Displacement of [125I]ghrelin from ovine recombinant GHSR1a expressed in HEK293F cells after 6 hrs by scintillation proximity assay				J Med Chem 50: 5202-16 (2007) Article DOI: 10.1021/jm070071+ BindingDB Entry DOI: 10.7270/Q2WH2QT2
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2C (Homo sapiens (Human))	BDBM50222866 (6-(4-chlorophenyl)-3-[(1-isopropylpiperidin-3-yl)m...) Show SMILES CC(C)N1CCC[C@H](Cn2cnc3ccc(cc3c2=O)-c2ccc(Cl)cc2)C1 Show InChI InChI=1S/C23H26ClN3O/c1-16(2)26-11-3-4-17(13-26)14-27-15-25-22-10-7-19(12-21(22)23(27)28)18-5-8-20(24)9-6-18/h5-10,12,15-17H,3-4,11,13-14H2,1-2H3/t17-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Bayer Pharmaceuticals Corporation Curated by ChEMBL					Assay Description Displacement of [125I]DIO from 5HT2c receptor				J Med Chem 50: 5202-16 (2007) Article DOI: 10.1021/jm070071+ BindingDB Entry DOI: 10.7270/Q2WH2QT2
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50222866 (6-(4-chlorophenyl)-3-[(1-isopropylpiperidin-3-yl)m...) Show SMILES CC(C)N1CCC[C@H](Cn2cnc3ccc(cc3c2=O)-c2ccc(Cl)cc2)C1 Show InChI InChI=1S/C23H26ClN3O/c1-16(2)26-11-3-4-17(13-26)14-27-15-25-22-10-7-19(12-21(22)23(27)28)18-5-8-20(24)9-6-18/h5-10,12,15-17H,3-4,11,13-14H2,1-2H3/t17-/m0/s1	PDB UniProtKB/SwissProt UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	200	n/a	n/a	n/a	n/a	n/a	n/a
Bayer Pharmaceuticals Corporation Curated by ChEMBL					Assay Description Inhibition of CYP2D6				J Med Chem 50: 5202-16 (2007) Article DOI: 10.1021/jm070071+ BindingDB Entry DOI: 10.7270/Q2WH2QT2
					More data for this Ligand-Target Pair