Compile Data Set for Download or QSAR

Found 3 hits of ic50 data for polymerid = 49000837   

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 (RAT)	BDBM50065468 (2-(4-Chloro-phenoxymethyl)-4-(3-piperidin-1-yl-pro...) Show SMILES Clc1ccc(OCc2nc3c(OCCCN4CCCCC4)cccc3n2CCCC2CCCNC2)cc1 Show InChI InChI=1S/C30H41ClN4O2/c31-25-12-14-26(15-13-25)37-23-29-33-30-27(35(29)20-6-9-24-8-5-16-32-22-24)10-4-11-28(30)36-21-7-19-34-17-2-1-3-18-34/h4,10-15,24,32H,1-3,5-9,16-23H2	PDB Reactome pathway UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.70	n/a	n/a	n/a	n/a	n/a	n/a
The R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description The compound was tested for the binding affinity against Neuropeptide Y receptor type 1 in rat				J Med Chem 42: 181-201 (1999) Article DOI: 10.1021/jm980521l BindingDB Entry DOI: 10.7270/Q2T43S8P
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (RAT)	BDBM50073048 (2-[4-(2-Oxo-2,3-dihydro-benzoimidazol-1-yl)-piperi...) Show SMILES O=C(CN1CCC(CC1)n1c2ccccc2[nH]c1=O)Nc1ccc2C(=O)c3ccccc3-c2c1 Show InChI InChI=1S/C27H24N4O3/c32-25(28-17-9-10-21-22(15-17)19-5-1-2-6-20(19)26(21)33)16-30-13-11-18(12-14-30)31-24-8-4-3-7-23(24)29-27(31)34/h1-10,15,18H,11-14,16H2,(H,28,32)(H,29,34)	PDB Reactome pathway UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	>5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
The R. W. Johnson Pharmaceutical Research Institute Curated by ChEMBL					Assay Description The compound was tested for the binding affinity against NPY1 (Neuropeptide Y receptor type 1)				J Med Chem 42: 181-201 (1999) Article DOI: 10.1021/jm980521l BindingDB Entry DOI: 10.7270/Q2T43S8P
					More data for this Ligand-Target Pair
Neuropeptide Y receptor type 1 (RAT)	BDBM50478529 (CHEMBL518564) Show SMILES [Na;v0+].[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-c1cc(-[#8]S([#8-])(=O)=O)ccc1-[#8] Show InChI InChI=1S/C31H46O5S/c1-24(2)11-7-12-25(3)13-8-14-26(4)15-9-16-27(5)17-10-18-28(6)19-20-29-23-30(21-22-31(29)32)36-37(33,34)35/h11,13,15,17,19,21-23,32H,7-10,12,14,16,18,20H2,1-6H3,(H,33,34,35)/p-1/b25-13+,26-15+,27-17+,28-19+	PDB Reactome pathway UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article	n/a	n/a	9.19E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Displacement of [3H]NPY from neuropeptide Y receptor in rat cerebral cortices				Citation and Details Article DOI: 10.1021/np50123a017 BindingDB Entry DOI: 10.7270/Q2514219
					More data for this Ligand-Target Pair