Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Serine/threonine-protein kinase 3' and Ligand = 'BDBM451763'   

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
Serine/threonine-protein kinase 3 (Homo sapiens (Human))	BDBM451763 (6-(2-amino-5-(4- chlorothiazol-5-yl)pyridin-3- yl)...) Show SMILES Nc1ncc(cc1-c1ccc2C(=O)NCCc2c1)-c1scnc1Cl Show InChI InChI=1S/C17H13ClN4OS/c18-15-14(24-8-22-15)11-6-13(16(19)21-7-11)9-1-2-12-10(5-9)3-4-20-17(12)23/h1-2,5-8H,3-4H2,(H2,19,21)(H,20,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	120	n/a	n/a	n/a	n/a	n/a	n/a
DANA-FARBER CANCER INSTITUTE, INC.; FONDAZIONE CENTRO SAN RAFFAELE US Patent					Assay Description Biochemical IC50s were measured at Invitrogen using Z-lyte technology. Briefly, for STK4, the 2×STK4 (MST1)/Ser/Thr 07 mixture was prepared in 50 mM ...				US Patent US10710978 (2020) BindingDB Entry DOI: 10.7270/Q2J67KZW
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase 3 (Homo sapiens (Human))	BDBM451763 (6-(2-amino-5-(4- chlorothiazol-5-yl)pyridin-3- yl)...) Show SMILES Nc1ncc(cc1-c1ccc2C(=O)NCCc2c1)-c1scnc1Cl Show InChI InChI=1S/C17H13ClN4OS/c18-15-14(24-8-22-15)11-6-13(16(19)21-7-11)9-1-2-12-10(5-9)3-4-20-17(12)23/h1-2,5-8H,3-4H2,(H2,19,21)(H,20,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
DANA-FARBER CANCER INSTITUTE, INC.; FONDAZIONE CENTRO SAN RAFFAELE US Patent					Assay Description Biochemical IC50s were measured at Invitrogen using Z-lyte technology. Briefly, for STK4, the 2×STK4 (MST1)/Ser/Thr 07 mixture was prepared in 50 mM ...				US Patent US10710978 (2020) BindingDB Entry DOI: 10.7270/Q2J67KZW
					More data for this Ligand-Target Pair