Compile Data Set for Download or QSAR

Found 2 hits of ic50 for monomerid = 50306090   

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
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human))	BDBM50306090 ((S)-1-(5-(3-methyl-1H-indazol-5-yl)-6-phenylpyridi...) Show SMILES Cc1n[nH]c2ccc(cc12)-c1cc(OC[C@@H](N)Cc2ccccc2)cnc1-c1ccccc1 |r| Show InChI InChI=1S/C28H26N4O/c1-19-25-15-22(12-13-27(25)32-31-19)26-16-24(17-30-28(26)21-10-6-3-7-11-21)33-18-23(29)14-20-8-4-2-5-9-20/h2-13,15-17,23H,14,18,29H2,1H3,(H,31,32)/t23-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	50	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Inhibition of full length AKT1				Bioorg Med Chem Lett 20: 673-8 (2010) Article DOI: 10.1016/j.bmcl.2009.11.064 BindingDB Entry DOI: 10.7270/Q2D21XQ0
					More data for this Ligand-Target Pair
Rho-associated protein kinase 1 (Homo sapiens (Human))	BDBM50306090 ((S)-1-(5-(3-methyl-1H-indazol-5-yl)-6-phenylpyridi...) Show SMILES Cc1n[nH]c2ccc(cc12)-c1cc(OC[C@@H](N)Cc2ccccc2)cnc1-c1ccccc1 |r| Show InChI InChI=1S/C28H26N4O/c1-19-25-15-22(12-13-27(25)32-31-19)26-16-24(17-30-28(26)21-10-6-3-7-11-21)33-18-23(29)14-20-8-4-2-5-9-20/h2-13,15-17,23H,14,18,29H2,1H3,(H,31,32)/t23-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Inhibition of ROCK1				Bioorg Med Chem Lett 20: 673-8 (2010) Article DOI: 10.1016/j.bmcl.2009.11.064 BindingDB Entry DOI: 10.7270/Q2D21XQ0
					More data for this Ligand-Target Pair