BDBM50344062 6-Bromo-8-hydroxy-3-(4'-hydroxyphenyl)coumarin::CHEMBL1777849
SMILES: Oc1ccc(cc1)-c1cc2cc(Br)cc(O)c2oc1=O
InChI Key: InChIKey=JRNZENXEHYOMCY-UHFFFAOYSA-N
Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Tyrosinase (Agaricus bisporus (Common mushroom)) | BDBM50344062 (6-Bromo-8-hydroxy-3-(4'-hydroxyphenyl)coumarin | C...) | UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 1.89E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universidad de Santiago de Compostela Curated by ChEMBL | Assay Description Non-competitive inhibition of mushroom tyrosinase using L-3,4- dihydroxyphenylalanine as substrate by Lineweaver-Burk double reciprocal plot analysis | Bioorg Med Chem Lett 21: 3342-5 (2011) Article DOI: 10.1016/j.bmcl.2011.04.012 BindingDB Entry DOI: 10.7270/Q2QF8T68 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Amine oxidase (flavin-containing) A (Homo sapiens (Human)) | BDBM50344062 (6-Bromo-8-hydroxy-3-(4'-hydroxyphenyl)coumarin | C...) | PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 2.07E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Universidad de Santiago de Compostela Curated by ChEMBL | Assay Description Inhibition of human recombinant MAO-A using p-tyramine substrate by flurometric method | Bioorg Med Chem Lett 21: 4224-7 (2011) Article DOI: 10.1016/j.bmcl.2011.05.074 BindingDB Entry DOI: 10.7270/Q27H1JX2 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Amine oxidase [flavin-containing] B (Homo sapiens (Human)) | BDBM50344062 (6-Bromo-8-hydroxy-3-(4'-hydroxyphenyl)coumarin | C...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1.69E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Universidad de Santiago de Compostela Curated by ChEMBL | Assay Description Inhibition of human recombinant MAO-B using p-tyramine substrate by flurometric method | Bioorg Med Chem Lett 21: 4224-7 (2011) Article DOI: 10.1016/j.bmcl.2011.05.074 BindingDB Entry DOI: 10.7270/Q27H1JX2 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Tyrosinase (Agaricus bisporus (Common mushroom)) | BDBM50344062 (6-Bromo-8-hydroxy-3-(4'-hydroxyphenyl)coumarin | C...) | UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 2.15E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Universidad de Santiago de Compostela Curated by ChEMBL | Assay Description Inhibition of mushroom tyrosinase using L-3,4- dihydroxyphenylalanine as substrate measured for 5 mins by spectrophotometric analysis | Bioorg Med Chem Lett 21: 3342-5 (2011) Article DOI: 10.1016/j.bmcl.2011.04.012 BindingDB Entry DOI: 10.7270/Q2QF8T68 | |||||||||||
More data for this Ligand-Target Pair |