Compile Data Set for Download or QSAR

Found 2 hits of kd for UniProtKB: A0A024RAV7   

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
Potassium channel, inwardly rectifying, subfamily J, member 11/Sulfonylurea receptor 2 (Homo sapiens-HUMAN)	BDBM50099576 (1-(4-Imidazol-1-yl-benzoyl)-cyclobutanecarbothioic...) Show SMILES CNC(=S)C1(CCC1)C(=O)c1ccc(cc1)-n1ccnc1 Show InChI InChI=1S/C16H17N3OS/c1-17-15(21)16(7-2-8-16)14(20)12-3-5-13(6-4-12)19-10-9-18-11-19/h3-6,9-11H,2,7-8H2,1H3,(H,17,21)	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	n/a	5.20E+3	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of SUR2B/Kir6.2				J Med Chem 44: 1627-53 (2001) Article DOI: 10.1021/jm000484+ BindingDB Entry DOI: 10.7270/Q218376D
					More data for this Ligand-Target Pair
Potassium channel, inwardly rectifying, subfamily J, member 11/Sulfonylurea receptor 2 (Homo sapiens-HUMAN)	BDBM50099576 (1-(4-Imidazol-1-yl-benzoyl)-cyclobutanecarbothioic...) Show SMILES CNC(=S)C1(CCC1)C(=O)c1ccc(cc1)-n1ccnc1 Show InChI InChI=1S/C16H17N3OS/c1-17-15(21)16(7-2-8-16)14(20)12-3-5-13(6-4-12)19-10-9-18-11-19/h3-6,9-11H,2,7-8H2,1H3,(H,17,21)	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	n/a	8.50E+3	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of SUR2B/Kir6.2				J Med Chem 44: 1627-53 (2001) Article DOI: 10.1021/jm000484+ BindingDB Entry DOI: 10.7270/Q218376D
					More data for this Ligand-Target Pair