Compile Data Set for Download or QSAR

Found 23 hits Enz. Inhib. hit(s) with all data for entry = 50029750   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/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))	BDBM50287527 (6-(2-Isopropyl-benzenesulfonyl)-5-nitro-quinolin-8...) Show SMILES CC(C)c1ccccc1S(=O)(=O)c1cc(N)c2ncccc2c1[N+]([O-])=O Show InChI InChI=1S/C18H17N3O4S/c1-11(2)12-6-3-4-8-15(12)26(24,25)16-10-14(19)17-13(7-5-9-20-17)18(16)21(22)23/h3-11H,19H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article	48	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287536 (6-(2-Fluoro-benzenesulfonyl)-5-nitro-quinolin-8-yl...) Show SMILES Nc1cc(c([N+]([O-])=O)c2cccnc12)S(=O)(=O)c1ccccc1F Show InChI InChI=1S/C15H10FN3O4S/c16-10-5-1-2-6-12(10)24(22,23)13-8-11(17)14-9(4-3-7-18-14)15(13)19(20)21/h1-8H,17H2	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	58	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287529 (6-(2-Chloro-benzenesulfonyl)-5-nitro-quinolin-8-yl...) Show SMILES Nc1cc(c([N+]([O-])=O)c2cccnc12)S(=O)(=O)c1ccccc1Cl Show InChI InChI=1S/C15H10ClN3O4S/c16-10-5-1-2-6-12(10)24(22,23)13-8-11(17)14-9(4-3-7-18-14)15(13)19(20)21/h1-8H,17H2	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	93	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287541 (5-Nitro-6-(toluene-2-sulfonyl)-quinolin-8-ylamine ...) Show SMILES Cc1ccccc1S(=O)(=O)c1cc(N)c2ncccc2c1[N+]([O-])=O Show InChI InChI=1S/C16H13N3O4S/c1-10-5-2-3-7-13(10)24(22,23)14-9-12(17)15-11(6-4-8-18-15)16(14)19(20)21/h2-9H,17H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	119	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287538 (6-(2-Ethyl-benzenesulfonyl)-5-nitro-quinolin-8-yla...) Show SMILES CCc1ccccc1S(=O)(=O)c1cc(N)c2ncccc2c1[N+]([O-])=O Show InChI InChI=1S/C17H15N3O4S/c1-2-11-6-3-4-8-14(11)25(23,24)15-10-13(18)16-12(7-5-9-19-16)17(15)20(21)22/h3-10H,2,18H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	129	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287534 (6-(2-Bromo-benzenesulfonyl)-5-nitro-quinolin-8-yla...) Show SMILES Nc1cc(c([N+]([O-])=O)c2cccnc12)S(=O)(=O)c1ccccc1Br Show InChI InChI=1S/C15H10BrN3O4S/c16-10-5-1-2-6-12(10)24(22,23)13-8-11(17)14-9(4-3-7-18-14)15(13)19(20)21/h1-8H,17H2	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	234	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287526 (6-(4-Amino-benzenesulfonyl)-5-nitro-quinolin-8-yla...) Show SMILES Nc1ccc(cc1)S(=O)(=O)c1cc(N)c2ncccc2c1[N+]([O-])=O Show InChI InChI=1S/C15H12N4O4S/c16-9-3-5-10(6-4-9)24(22,23)13-8-12(17)14-11(2-1-7-18-14)15(13)19(20)21/h1-8H,16-17H2	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	282	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287539 (6-Benzenesulfonyl-5-nitro-quinolin-8-ylamine | CHE...) Show SMILES Nc1cc(c([N+]([O-])=O)c2cccnc12)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C15H11N3O4S/c16-12-9-13(23(21,22)10-5-2-1-3-6-10)15(18(19)20)11-7-4-8-17-14(11)12/h1-9H,16H2	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	297	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287530 (5-Nitro-6-(toluene-4-sulfonyl)-quinolin-8-ylamine ...) Show SMILES Cc1ccc(cc1)S(=O)(=O)c1cc(N)c2ncccc2c1[N+]([O-])=O Show InChI InChI=1S/C16H13N3O4S/c1-10-4-6-11(7-5-10)24(22,23)14-9-13(17)15-12(3-2-8-18-15)16(14)19(20)21/h2-9H,17H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	594	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287525 (6-(3-Chloro-benzenesulfonyl)-5-nitro-quinolin-8-yl...) Show SMILES Nc1cc(c([N+]([O-])=O)c2cccnc12)S(=O)(=O)c1cccc(Cl)c1 Show InChI InChI=1S/C15H10ClN3O4S/c16-9-3-1-4-10(7-9)24(22,23)13-8-12(17)14-11(5-2-6-18-14)15(13)19(20)21/h1-8H,17H2	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	892	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287528 (6-(4-Methoxy-benzenesulfonyl)-5-nitro-quinolin-8-y...) Show SMILES COc1ccc(cc1)S(=O)(=O)c1cc(N)c2ncccc2c1[N+]([O-])=O Show InChI InChI=1S/C16H13N3O5S/c1-24-10-4-6-11(7-5-10)25(22,23)14-9-13(17)15-12(3-2-8-18-15)16(14)19(20)21/h2-9H,17H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	1.14E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287533 (6-(4-Amino-benzenesulfinyl)-5-nitro-quinolin-8-yla...) Show SMILES Nc1ccc(cc1)S(=O)c1cc(N)c2ncccc2c1[N+]([O-])=O Show InChI InChI=1S/C15H12N4O3S/c16-9-3-5-10(6-4-9)23(22)13-8-12(17)14-11(2-1-7-18-14)15(13)19(20)21/h1-8H,16-17H2	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	1.25E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287532 (6-(4-Chloro-benzenesulfonyl)-5-nitro-quinolin-8-yl...) Show SMILES Nc1cc(c([N+]([O-])=O)c2cccnc12)S(=O)(=O)c1ccc(Cl)cc1 Show InChI InChI=1S/C15H10ClN3O4S/c16-9-3-5-10(6-4-9)24(22,23)13-8-12(17)14-11(2-1-7-18-14)15(13)19(20)21/h1-8H,17H2	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	1.75E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287540 (CHEMBL54289 | N-(8-Amino-5-nitro-quinolin-6-yl)-be...) Show SMILES Nc1cc(NS(=O)(=O)c2ccccc2)c([N+]([O-])=O)c2cccnc12 Show InChI InChI=1S/C15H12N4O4S/c16-12-9-13(18-24(22,23)10-5-2-1-3-6-10)15(19(20)21)11-7-4-8-17-14(11)12/h1-9,18H,16H2	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287537 (6-(4-Amino-phenylsulfanyl)-5-nitro-quinolin-8-ylam...) Show SMILES Nc1ccc(Sc2cc(N)c3ncccc3c2[N+]([O-])=O)cc1 Show InChI InChI=1S/C15H12N4O2S/c16-9-3-5-10(6-4-9)22-13-8-12(17)14-11(2-1-7-18-14)15(13)19(20)21/h1-8H,16-17H2	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287535 (4-(5-Nitro-quinoline-6-sulfonyl)-phenylamine | CHE...) Show SMILES Nc1ccc(cc1)S(=O)(=O)c1ccc2ncccc2c1[N+]([O-])=O Show InChI InChI=1S/C15H11N3O4S/c16-10-3-5-11(6-4-10)23(21,22)14-8-7-13-12(2-1-9-17-13)15(14)18(19)20/h1-9H,16H2	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287531 ((6-Benzenesulfonyl-5-nitro-quinolin-8-yl)-methyl-a...) Show SMILES CNc1cc(c([N+]([O-])=O)c2cccnc12)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C16H13N3O4S/c1-17-13-10-14(24(22,23)11-6-3-2-4-7-11)16(19(20)21)12-8-5-9-18-15(12)13/h2-10,17H,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 2 (RAT)	BDBM50287526 (6-(4-Amino-benzenesulfonyl)-5-nitro-quinolin-8-yla...) Show SMILES Nc1ccc(cc1)S(=O)(=O)c1cc(N)c2ncccc2c1[N+]([O-])=O Show InChI InChI=1S/C15H12N4O4S/c16-9-3-5-10(6-4-9)24(22,23)13-8-12(17)14-11(2-1-7-18-14)15(13)19(20)21/h1-8H,16-17H2	PDB Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y2 (NPY2) receptor from rat hippocampi.				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287524 (6-(4-Amino-benzenesulfonyl)-quinolin-8-ylamine | C...) Show SMILES Nc1ccc(cc1)S(=O)(=O)c1cc(N)c2ncccc2c1 Show InChI InChI=1S/C15H13N3O2S/c16-11-3-5-12(6-4-11)21(19,20)13-8-10-2-1-7-18-15(10)14(17)9-13/h1-9H,16-17H2	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287542 (6-Methanesulfonyl-5-nitro-quinolin-8-ylamine | CHE...) Show SMILES CS(=O)(=O)c1cc(N)c2ncccc2c1[N+]([O-])=O Show InChI InChI=1S/C10H9N3O4S/c1-18(16,17)8-5-7(11)9-6(3-2-4-12-9)10(8)13(14)15/h2-5H,11H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287522 (6-(4-Amino-benzenesulfonyl)-quinoline-5,8-diamine ...) Show SMILES Nc1ccc(cc1)S(=O)(=O)c1cc(N)c2ncccc2c1N Show InChI InChI=1S/C15H14N4O2S/c16-9-3-5-10(6-4-9)22(20,21)13-8-12(17)15-11(14(13)18)2-1-7-19-15/h1-8H,16-18H2	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (Homo sapiens (Human))	BDBM50287523 (6-Benzenesulfonyl-8-methyl-5-nitro-quinoline | CHE...) Show SMILES Cc1cc(c([N+]([O-])=O)c2cccnc12)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C16H12N2O4S/c1-11-10-14(23(21,22)12-6-3-2-4-7-12)16(18(19)20)13-8-5-9-17-15(11)13/h2-10H,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y1 (NPY1) receptor from SK-N-MC membranes using [125I]-PYY as radioligand				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 2 (RAT)	BDBM50287527 (6-(2-Isopropyl-benzenesulfonyl)-5-nitro-quinolin-8...) Show SMILES CC(C)c1ccccc1S(=O)(=O)c1cc(N)c2ncccc2c1[N+]([O-])=O Show InChI InChI=1S/C18H17N3O4S/c1-11(2)12-6-3-4-8-15(12)26(24,25)16-10-14(19)17-13(7-5-9-20-17)18(16)21(22)23/h3-11H,19H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for binding affinity against neuropeptide Y2 (NPY2) receptor from rat hippocampi.				Bioorg Med Chem Lett 6: 1809-1814 (1996) Article DOI: 10.1016/0960-894X(96)00319-8 BindingDB Entry DOI: 10.7270/Q2M045FM
					More data for this Ligand-Target Pair