null

SMILES: CN(C)C1CCN(CCc2c(COc3ccc(Br)cc3CO)sc3ccccc23)CC1

InChI Key: InChIKey=VSDGMNFJZBSRSC-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50075231   

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
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50075231 ((5-Bromo-2-{3-[2-(4-dimethylamino-piperidin-1-yl)-...) Show SMILES CN(C)C1CCN(CCc2c(COc3ccc(Br)cc3CO)sc3ccccc23)CC1 Show InChI InChI=1S/C25H31BrN2O2S/c1-27(2)20-9-12-28(13-10-20)14-11-22-21-5-3-4-6-24(21)31-25(22)17-30-23-8-7-19(26)15-18(23)16-29/h3-8,15,20,29H,9-14,16-17H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	15	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Ability to displace [125I]-pPYY from AV12 cell line stably transfected with cloned human neuropeptide Y receptor type 1.				Bioorg Med Chem Lett 9: 475-80 (1999) BindingDB Entry DOI: 10.7270/Q2K35ST3
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50075231 ((5-Bromo-2-{3-[2-(4-dimethylamino-piperidin-1-yl)-...) Show SMILES CN(C)C1CCN(CCc2c(COc3ccc(Br)cc3CO)sc3ccccc23)CC1 Show InChI InChI=1S/C25H31BrN2O2S/c1-27(2)20-9-12-28(13-10-20)14-11-22-21-5-3-4-6-24(21)31-25(22)17-30-23-8-7-19(26)15-18(23)16-29/h3-8,15,20,29H,9-14,16-17H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.20E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Ability to displace [125I]-pPYY from AV12 cell line stably transfected with cloned human neuropeptide Y receptor type 1.				Bioorg Med Chem Lett 9: 475-80 (1999) BindingDB Entry DOI: 10.7270/Q2K35ST3
					More data for this Ligand-Target Pair