null

SMILES: C[C@H]([C@@H](O)c1ccccc1)N(C)C(=O)Nc1ccc(Oc2ccc(C)c(C)c2)cc1

InChI Key: InChIKey=GDLDMMQGPKEHMY-NTKDMRAZSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50101542   

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))	BDBM50101542 (3-[4-(3,4-Dimethyl-phenoxy)-phenyl]-1-(2-hydroxy-1...) Show SMILES C[C@H]([C@@H](O)c1ccccc1)N(C)C(=O)Nc1ccc(Oc2ccc(C)c(C)c2)cc1 Show InChI InChI=1S/C25H28N2O3/c1-17-10-13-23(16-18(17)2)30-22-14-11-21(12-15-22)26-25(29)27(4)19(3)24(28)20-8-6-5-7-9-20/h5-16,19,24,28H,1-4H3,(H,26,29)/t19-,24-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Amgen Inc. Curated by ChEMBL					Assay Description Inhibitory activity tested against Human Neuropeptide Y1 Receptor.				J Med Chem 44: 2344-56 (2001) BindingDB Entry DOI: 10.7270/Q2DV1J56
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 2 (Homo sapiens (Human))	BDBM50101542 (3-[4-(3,4-Dimethyl-phenoxy)-phenyl]-1-(2-hydroxy-1...) Show SMILES C[C@H]([C@@H](O)c1ccccc1)N(C)C(=O)Nc1ccc(Oc2ccc(C)c(C)c2)cc1 Show InChI InChI=1S/C25H28N2O3/c1-17-10-13-23(16-18(17)2)30-22-14-11-21(12-15-22)26-25(29)27(4)19(3)24(28)20-8-6-5-7-9-20/h5-16,19,24,28H,1-4H3,(H,26,29)/t19-,24-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Amgen Inc. Curated by ChEMBL					Assay Description Inhibitory activity tested against Human Neuropeptide Y2 Receptor.				J Med Chem 44: 2344-56 (2001) BindingDB Entry DOI: 10.7270/Q2DV1J56
					More data for this Ligand-Target Pair