Compile Data Set for Download or QSAR

Found 3 hits of ic50 for monomerid = 50393556   

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
Macrophage colony-stimulating factor 1 receptor (Homo sapiens (Human))	BDBM50393556 (CHEMBL2158296) Show SMILES O=C(Cc1cccnc1)N1CCC(CC1)c1ccc(NC(=O)c2ncc([nH]2)C#N)c(c1)C1=CCCCC1 |t:35| Show InChI InChI=1S/C29H30N6O2/c30-17-24-19-32-28(33-24)29(37)34-26-9-8-23(16-25(26)22-6-2-1-3-7-22)21-10-13-35(14-11-21)27(36)15-20-5-4-12-31-18-20/h4-6,8-9,12,16,18-19,21H,1-3,7,10-11,13-15H2,(H,32,33)(H,34,37)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.70	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Inhibition of FMS mediated phosphorylation using SYEGNSYTFIDPTQ as substrate after 80 mins by fluorescence polarization				J Med Chem 54: 7860-83 (2011) Article DOI: 10.1021/jm200900q BindingDB Entry DOI: 10.7270/Q2VD70JB
					More data for this Ligand-Target Pair
Macrophage colony-stimulating factor 1 receptor (Mus musculus (Mouse))	BDBM50393556 (CHEMBL2158296) Show SMILES O=C(Cc1cccnc1)N1CCC(CC1)c1ccc(NC(=O)c2ncc([nH]2)C#N)c(c1)C1=CCCCC1 |t:35| Show InChI InChI=1S/C29H30N6O2/c30-17-24-19-32-28(33-24)29(37)34-26-9-8-23(16-25(26)22-6-2-1-3-7-22)21-10-13-35(14-11-21)27(36)15-20-5-4-12-31-18-20/h4-6,8-9,12,16,18-19,21H,1-3,7,10-11,13-15H2,(H,32,33)(H,34,37)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.10	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Inhibition of FMS-mediated proliferation in CSF1-stimulated bone marrow-derived mouse macrophages assessed as inhibition of incorporation of bromodeo...				J Med Chem 54: 7860-83 (2011) Article DOI: 10.1021/jm200900q BindingDB Entry DOI: 10.7270/Q2VD70JB
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50393556 (CHEMBL2158296) Show SMILES O=C(Cc1cccnc1)N1CCC(CC1)c1ccc(NC(=O)c2ncc([nH]2)C#N)c(c1)C1=CCCCC1 |t:35| Show InChI InChI=1S/C29H30N6O2/c30-17-24-19-32-28(33-24)29(37)34-26-9-8-23(16-25(26)22-6-2-1-3-7-22)21-10-13-35(14-11-21)27(36)15-20-5-4-12-31-18-20/h4-6,8-9,12,16,18-19,21H,1-3,7,10-11,13-15H2,(H,32,33)(H,34,37)	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	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]astemizole from human ERG potassium channel				J Med Chem 54: 7860-83 (2011) Article DOI: 10.1021/jm200900q BindingDB Entry DOI: 10.7270/Q2VD70JB
					More data for this Ligand-Target Pair