Compile Data Set for Download or QSAR

Found 3 hits of ki data for polymerid = 50002911,50003466   

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
Beta-xylosidase (Thermoanaerobacter saccharolyticum)	BDBM50182802 (5-(dimethylamino)-N-(6-((3R,4r,5S)-3,4,5-trihydrox...) Show SMILES CN(C)c1cccc2c(cccc12)S(=O)(=O)NCCCCCCN1C[C@H](O)[C@@H](O)[C@H](O)C1 Show InChI InChI=1S/C23H35N3O5S/c1-25(2)19-11-7-10-18-17(19)9-8-12-22(18)32(30,31)24-13-5-3-4-6-14-26-15-20(27)23(29)21(28)16-26/h7-12,20-21,23-24,27-29H,3-6,13-16H2,1-2H3/t20-,21+,23+	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.60E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Technische Universität Graz Curated by ChEMBL					Assay Description Inhibition of Thermoanaerobacterium saccharolyticum beta-xylosidase				Bioorg Med Chem Lett 16: 2067-70 (2006) Article DOI: 10.1016/j.bmcl.2006.01.095 BindingDB Entry DOI: 10.7270/Q26Q1WV2
					More data for this Ligand-Target Pair
Beta-xylosidase (Thermoanaerobacter saccharolyticum)	BDBM50182798 ((3R,4r,5S)-piperidine-3,4,5-triol | 1,5-Dideoxy-1,...) Show SMILES O[C@H]1CNC[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C5H11NO3/c7-3-1-6-2-4(8)5(3)9/h3-9H,1-2H2/t3-,4+,5+	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	2.06E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Technische Universität Graz Curated by ChEMBL					Assay Description Inhibition of Thermoanaerobacterium saccharolyticum beta-xylosidase				Bioorg Med Chem Lett 16: 2067-70 (2006) Article DOI: 10.1016/j.bmcl.2006.01.095 BindingDB Entry DOI: 10.7270/Q26Q1WV2
					More data for this Ligand-Target Pair
Exo-1,4-beta-xylosidase xlnD (Aspergillus niger)	BDBM50096896 (2-phenyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)tet...) Show SMILES N\C(Cc1ccccc1)=[NH+]/C1OC(CO)C(O)C(O)C1O Show InChI InChI=1S/C14H20N2O5/c15-10(6-8-4-2-1-3-5-8)16-14-13(20)12(19)11(18)9(7-17)21-14/h1-5,9,11-14,17-20H,6-7H2,(H2,15,16)/p+1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto University Curated by ChEMBL					Assay Description Compound was evaluated for the selective and competitive inhibition of Beta-xylosidase from A. pulverulentus				Bioorg Med Chem Lett 11: 467-70 (2001) BindingDB Entry DOI: 10.7270/Q2R210N1
					More data for this Ligand-Target Pair