Compile Data Set for Download or QSAR

Found 1 hit Enz. Inhib. hit(s) with Target = 'M-phase inducer phosphatase 2' and Ligand = 'BDBM50402669'   

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
M-phase inducer phosphatase 2 (Homo sapiens (Human))	BDBM50402669 (CHEMBL2206730) Show SMILES Oc1ccc(C=C2SC(NCCCn3cc(CCNC4=NC(=O)C(S4)=Cc4ccc(O)cc4)nn3)=NC2=O)cc1 |w:5.4,25.26,c:37,t:19| Show InChI InChI=1S/C27H25N7O4S2/c35-20-6-2-17(3-7-20)14-22-24(37)30-26(39-22)28-11-1-13-34-16-19(32-33-34)10-12-29-27-31-25(38)23(40-27)15-18-4-8-21(36)9-5-18/h2-9,14-16,35-36H,1,10-13H2,(H,28,30,37)(H,29,31,38)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.06E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ Paris Descartes Curated by ChEMBL					Assay Description Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...				Bioorg Med Chem Lett 22: 7345-50 (2012) Article DOI: 10.1016/j.bmcl.2012.10.072 BindingDB Entry DOI: 10.7270/Q2J67J38
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