null

SMILES: C[C@H]([C@@H](O)c1ccccc1)N(C)C(=O)Nc1ccc(Oc2cccc(c2)[N+]([O-])=O)cc1

InChI Key: InChIKey=BGRKYPKEPNKVGH-OPAMFIHVSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50101559   

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 5 (Homo sapiens (Human))	BDBM50101559 (1-(2-Hydroxy-1-methyl-2-phenyl-ethyl)-1-methyl-3-[...) Show SMILES C[C@H]([C@@H](O)c1ccccc1)N(C)C(=O)Nc1ccc(Oc2cccc(c2)[N+]([O-])=O)cc1 Show InChI InChI=1S/C23H23N3O5/c1-16(22(27)17-7-4-3-5-8-17)25(2)23(28)24-18-11-13-20(14-12-18)31-21-10-6-9-19(15-21)26(29)30/h3-16,22,27H,1-2H3,(H,24,28)/t16-,22-/m1/s1	KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	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 Y5 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))	BDBM50101559 (1-(2-Hydroxy-1-methyl-2-phenyl-ethyl)-1-methyl-3-[...) Show SMILES C[C@H]([C@@H](O)c1ccccc1)N(C)C(=O)Nc1ccc(Oc2cccc(c2)[N+]([O-])=O)cc1 Show InChI InChI=1S/C23H23N3O5/c1-16(22(27)17-7-4-3-5-8-17)25(2)23(28)24-18-11-13-20(14-12-18)31-21-10-6-9-19(15-21)26(29)30/h3-16,22,27H,1-2H3,(H,24,28)/t16-,22-/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
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50101559 (1-(2-Hydroxy-1-methyl-2-phenyl-ethyl)-1-methyl-3-[...) Show SMILES C[C@H]([C@@H](O)c1ccccc1)N(C)C(=O)Nc1ccc(Oc2cccc(c2)[N+]([O-])=O)cc1 Show InChI InChI=1S/C23H23N3O5/c1-16(22(27)17-7-4-3-5-8-17)25(2)23(28)24-18-11-13-20(14-12-18)31-21-10-6-9-19(15-21)26(29)30/h3-16,22,27H,1-2H3,(H,24,28)/t16-,22-/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