Compile Data Set for Download or QSAR

Found 2 hits of ic50 for monomerid = 50323433   

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
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50323433 (4-(3-(3-tert-butyl-5-(3-phenylureido)-1H-pyrazol-1...) Show SMILES CC(C)(C)c1cc(NC(=O)Nc2ccccc2)n(n1)-c1cccc(CNC(=O)CCC(O)=O)c1 Show InChI InChI=1S/C25H29N5O4/c1-25(2,3)20-15-21(28-24(34)27-18-9-5-4-6-10-18)30(29-20)19-11-7-8-17(14-19)16-26-22(31)12-13-23(32)33/h4-11,14-15H,12-13,16H2,1-3H3,(H,26,31)(H,32,33)(H2,27,28,34)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	37	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Inc. Curated by ChEMBL					Assay Description Inhibition of unactive p38alpha				Bioorg Med Chem Lett 20: 4885-91 (2010) Article DOI: 10.1016/j.bmcl.2010.06.073 BindingDB Entry DOI: 10.7270/Q2Z31ZT2
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50323433 (4-(3-(3-tert-butyl-5-(3-phenylureido)-1H-pyrazol-1...) Show SMILES CC(C)(C)c1cc(NC(=O)Nc2ccccc2)n(n1)-c1cccc(CNC(=O)CCC(O)=O)c1 Show InChI InChI=1S/C25H29N5O4/c1-25(2,3)20-15-21(28-24(34)27-18-9-5-4-6-10-18)30(29-20)19-11-7-8-17(14-19)16-26-22(31)12-13-23(32)33/h4-11,14-15H,12-13,16H2,1-3H3,(H,26,31)(H,32,33)(H2,27,28,34)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	393	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Inc. Curated by ChEMBL					Assay Description Inhibition of active p38alpha				Bioorg Med Chem Lett 20: 4885-91 (2010) Article DOI: 10.1016/j.bmcl.2010.06.073 BindingDB Entry DOI: 10.7270/Q2Z31ZT2
					More data for this Ligand-Target Pair