Affinity Data by PubMed id=21033679

PubMed code 21033679

Found 6 hits of Enzyme Inhibition Constant Data
Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	k_off s^-1	k_on M^-1s^-1	pH	Temp °C
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50330259 (CHEMBL1236391 \| N-(3-(methylthio)-1-phenyl-1H-inda...) Show SMILES Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	8.13E+3	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of human ERG				J Med Chem 53: 7979-91 (2010) Article DOI: 10.1021/jm100677s BindingDB Entry DOI: 10.7270/Q2Z038D4
					More data for this Ligand-Target Pair
Cytochrome P450 2C9 (Homo sapiens (Human))	BDBM50330259 (CHEMBL1236391 \| N-(3-(methylthio)-1-phenyl-1H-inda...) Show SMILES Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem Patents 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 and Development Curated by ChEMBL					Assay Description Inhibition of human recombinant CYP2C9				J Med Chem 53: 7979-91 (2010) Article DOI: 10.1021/jm100677s BindingDB Entry DOI: 10.7270/Q2Z038D4
					More data for this Ligand-Target Pair
Cytochrome P450 2C19 (Homo sapiens (Human))	BDBM50330259 (CHEMBL1236391 \| N-(3-(methylthio)-1-phenyl-1H-inda...) Show SMILES Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem Patents 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 and Development Curated by ChEMBL					Assay Description Inhibition of human recombinant CYP2C19				J Med Chem 53: 7979-91 (2010) Article DOI: 10.1021/jm100677s BindingDB Entry DOI: 10.7270/Q2Z038D4
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50330259 (CHEMBL1236391 \| N-(3-(methylthio)-1-phenyl-1H-inda...) Show SMILES Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem Patents 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 and Development Curated by ChEMBL					Assay Description Inhibition of human recombinant CYP2D6				J Med Chem 53: 7979-91 (2010) Article DOI: 10.1021/jm100677s BindingDB Entry DOI: 10.7270/Q2Z038D4
					More data for this Ligand-Target Pair
Cytochrome P450 1A2 (Homo sapiens (Human))	BDBM50330259 (CHEMBL1236391 \| N-(3-(methylthio)-1-phenyl-1H-inda...) Show SMILES Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem Patents 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 and Development Curated by ChEMBL					Assay Description Inhibition of human recombinant CYP1A2				J Med Chem 53: 7979-91 (2010) Article DOI: 10.1021/jm100677s BindingDB Entry DOI: 10.7270/Q2Z038D4
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50330259 (CHEMBL1236391 \| N-(3-(methylthio)-1-phenyl-1H-inda...) Show SMILES Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem Patents 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 and Development Curated by ChEMBL					Assay Description Inhibition of human recombinant CYP3A4				J Med Chem 53: 7979-91 (2010) Article DOI: 10.1021/jm100677s BindingDB Entry DOI: 10.7270/Q2Z038D4
					More data for this Ligand-Target Pair

* indicates data uncertainty>20%