Compile Data Set for Download or QSAR

Found 2 hits of ki for monomerid = 50378784   

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
Orotidine 5'-phosphate decarboxylase (Saccharomyces cerevisiae)	BDBM50378784 (CHEMBL1164953) Show SMILES NC(=O)c1[nH]nc([C@@H]2O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]2O)c1O |r| Show InChI InChI=1S/C9H14N3O9P/c10-9(16)4-6(14)3(11-12-4)8-7(15)5(13)2(21-8)1-20-22(17,18)19/h2,5,7-8,13-15H,1H2,(H2,10,16)(H,11,12)(H2,17,18,19)/t2-,5-,7-,8+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem	Article PubMed	5	-47.4	n/a	n/a	n/a	n/a	n/a	n/a	25
University Health Network Curated by ChEMBL					Assay Description Inhibition of Saccharomyces cerevisia uridine 5'-monophosphate synthase after overnight incubation at room temperature by VP-ITC microcalorimetry				Bioorg Med Chem 18: 4032-41 (2010) Article DOI: 10.1016/j.bmc.2010.04.017 BindingDB Entry DOI: 10.7270/Q24T6KBX
					More data for this Ligand-Target Pair
Uridine 5'-monophosphate synthase (Homo sapiens (Human))	BDBM50378784 (CHEMBL1164953) Show SMILES NC(=O)c1[nH]nc([C@@H]2O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]2O)c1O |r| Show InChI InChI=1S/C9H14N3O9P/c10-9(16)4-6(14)3(11-12-4)8-7(15)5(13)2(21-8)1-20-22(17,18)19/h2,5,7-8,13-15H,1H2,(H2,10,16)(H,11,12)(H2,17,18,19)/t2-,5-,7-,8+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem	Article PubMed	17	-44.3	n/a	n/a	n/a	n/a	n/a	n/a	25
University Health Network Curated by ChEMBL					Assay Description Inhibition of human uridine 5'-monophosphate synthase after overnight incubation at room temperature by UV spectroscopy				Bioorg Med Chem 18: 4032-41 (2010) Article DOI: 10.1016/j.bmc.2010.04.017 BindingDB Entry DOI: 10.7270/Q24T6KBX
					More data for this Ligand-Target Pair