Compile Data Set for Download or QSAR

Found 5 hits of ic50 for monomerid = 50361006   

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
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50361006 (CHEMBL1935443) Show SMILES Cc1ccc(Cn2c(nc3ccccc23)C2CNCCO2)cc1C Show InChI InChI=1S/C20H23N3O/c1-14-7-8-16(11-15(14)2)13-23-18-6-4-3-5-17(18)22-20(23)19-12-21-9-10-24-19/h3-8,11,19,21H,9-10,12-13H2,1-2H3	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	2.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Neurocrine Biosciences Curated by ChEMBL					Assay Description Inhibition of human Erg by whole cell patch clamp electrophysiology				Bioorg Med Chem Lett 22: 421-6 (2011) Article DOI: 10.1016/j.bmcl.2011.10.115 BindingDB Entry DOI: 10.7270/Q2J103KS
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50361006 (CHEMBL1935443) Show SMILES Cc1ccc(Cn2c(nc3ccccc23)C2CNCCO2)cc1C Show InChI InChI=1S/C20H23N3O/c1-14-7-8-16(11-15(14)2)13-23-18-6-4-3-5-17(18)22-20(23)19-12-21-9-10-24-19/h3-8,11,19,21H,9-10,12-13H2,1-2H3	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	4.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Neurocrine Biosciences Curated by ChEMBL					Assay Description Inhibition of CYP3A4				Bioorg Med Chem Lett 22: 421-6 (2011) Article DOI: 10.1016/j.bmcl.2011.10.115 BindingDB Entry DOI: 10.7270/Q2J103KS
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50361006 (CHEMBL1935443) Show SMILES Cc1ccc(Cn2c(nc3ccccc23)C2CNCCO2)cc1C Show InChI InChI=1S/C20H23N3O/c1-14-7-8-16(11-15(14)2)13-23-18-6-4-3-5-17(18)22-20(23)19-12-21-9-10-24-19/h3-8,11,19,21H,9-10,12-13H2,1-2H3	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	4.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Neurocrine Biosciences Curated by ChEMBL					Assay Description Inhibition of CYP3A4				Bioorg Med Chem Lett 22: 421-6 (2011) Article DOI: 10.1016/j.bmcl.2011.10.115 BindingDB Entry DOI: 10.7270/Q2J103KS
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50361006 (CHEMBL1935443) Show SMILES Cc1ccc(Cn2c(nc3ccccc23)C2CNCCO2)cc1C Show InChI InChI=1S/C20H23N3O/c1-14-7-8-16(11-15(14)2)13-23-18-6-4-3-5-17(18)22-20(23)19-12-21-9-10-24-19/h3-8,11,19,21H,9-10,12-13H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Neurocrine Biosciences Curated by ChEMBL					Assay Description Inhibition of CYP2D6				Bioorg Med Chem Lett 22: 421-6 (2011) Article DOI: 10.1016/j.bmcl.2011.10.115 BindingDB Entry DOI: 10.7270/Q2J103KS
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50361006 (CHEMBL1935443) Show SMILES Cc1ccc(Cn2c(nc3ccccc23)C2CNCCO2)cc1C Show InChI InChI=1S/C20H23N3O/c1-14-7-8-16(11-15(14)2)13-23-18-6-4-3-5-17(18)22-20(23)19-12-21-9-10-24-19/h3-8,11,19,21H,9-10,12-13H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Neurocrine Biosciences Curated by ChEMBL					Assay Description Inhibition of CYP2D6				Bioorg Med Chem Lett 22: 421-6 (2011) Article DOI: 10.1016/j.bmcl.2011.10.115 BindingDB Entry DOI: 10.7270/Q2J103KS
					More data for this Ligand-Target Pair