Compile Data Set for Download or QSAR

Found 5 hits of ic50 for monomerid = 50334933   

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
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50334933 (1-({4-[6-Methyl-3-(trifluoromethyl)-4,5,6,7-tetrah...) Show SMILES CN1CCc2c(C1)n(nc2C(F)(F)F)-c1ccc(CN2CCCC2=O)cc1 Show InChI InChI=1S/C19H21F3N4O/c1-24-10-8-15-16(12-24)26(23-18(15)19(20,21)22)14-6-4-13(5-7-14)11-25-9-2-3-17(25)27/h4-7H,2-3,8-12H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Sussex Curated by ChEMBL					Assay Description Inhibition of human CYP3A4 by fluorescence assay				J Med Chem 54: 78-94 (2011) Article DOI: 10.1021/jm100679e BindingDB Entry DOI: 10.7270/Q21C1XVG
					More data for this Ligand-Target Pair
Cytochrome P450 1A2 (Homo sapiens (Human))	BDBM50334933 (1-({4-[6-Methyl-3-(trifluoromethyl)-4,5,6,7-tetrah...) Show SMILES CN1CCc2c(C1)n(nc2C(F)(F)F)-c1ccc(CN2CCCC2=O)cc1 Show InChI InChI=1S/C19H21F3N4O/c1-24-10-8-15-16(12-24)26(23-18(15)19(20,21)22)14-6-4-13(5-7-14)11-25-9-2-3-17(25)27/h4-7H,2-3,8-12H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Sussex Curated by ChEMBL					Assay Description Inhibition of human CYP1A2 by fluorescence assay				J Med Chem 54: 78-94 (2011) Article DOI: 10.1021/jm100679e BindingDB Entry DOI: 10.7270/Q21C1XVG
					More data for this Ligand-Target Pair
Cytochrome P450 2C19 (Homo sapiens (Human))	BDBM50334933 (1-({4-[6-Methyl-3-(trifluoromethyl)-4,5,6,7-tetrah...) Show SMILES CN1CCc2c(C1)n(nc2C(F)(F)F)-c1ccc(CN2CCCC2=O)cc1 Show InChI InChI=1S/C19H21F3N4O/c1-24-10-8-15-16(12-24)26(23-18(15)19(20,21)22)14-6-4-13(5-7-14)11-25-9-2-3-17(25)27/h4-7H,2-3,8-12H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Sussex Curated by ChEMBL					Assay Description Inhibition of human CYP2C19 by fluorescence assay				J Med Chem 54: 78-94 (2011) Article DOI: 10.1021/jm100679e BindingDB Entry DOI: 10.7270/Q21C1XVG
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50334933 (1-({4-[6-Methyl-3-(trifluoromethyl)-4,5,6,7-tetrah...) Show SMILES CN1CCc2c(C1)n(nc2C(F)(F)F)-c1ccc(CN2CCCC2=O)cc1 Show InChI InChI=1S/C19H21F3N4O/c1-24-10-8-15-16(12-24)26(23-18(15)19(20,21)22)14-6-4-13(5-7-14)11-25-9-2-3-17(25)27/h4-7H,2-3,8-12H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Sussex Curated by ChEMBL					Assay Description Inhibition of human CYP2D6 by fluorescence assay				J Med Chem 54: 78-94 (2011) Article DOI: 10.1021/jm100679e BindingDB Entry DOI: 10.7270/Q21C1XVG
					More data for this Ligand-Target Pair
Cytochrome P450 2C9 (Homo sapiens (Human))	BDBM50334933 (1-({4-[6-Methyl-3-(trifluoromethyl)-4,5,6,7-tetrah...) Show SMILES CN1CCc2c(C1)n(nc2C(F)(F)F)-c1ccc(CN2CCCC2=O)cc1 Show InChI InChI=1S/C19H21F3N4O/c1-24-10-8-15-16(12-24)26(23-18(15)19(20,21)22)14-6-4-13(5-7-14)11-25-9-2-3-17(25)27/h4-7H,2-3,8-12H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Sussex Curated by ChEMBL					Assay Description Inhibition of human CYP2C9 by fluorescence assay				J Med Chem 54: 78-94 (2011) Article DOI: 10.1021/jm100679e BindingDB Entry DOI: 10.7270/Q21C1XVG
					More data for this Ligand-Target Pair