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23 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review
PMIDDataArticle TitleOrganization
27145071 37 2-(3-Methoxyphenyl)quinazoline Derivatives: A New Class of Direct Constitutive Androstane Receptor (CAR) Agonists.EBI Palacky University In Olomouc
26101566 14 Optimization of ADME Properties for Sulfonamides Leading to the Discovery of a T-Type Calcium Channel Blocker, ABT-639.EBI Abbvie
24997686 9 Synthesis and biological evaluation of 2,3'-diindolylmethanes as agonists of aryl hydrocarbon receptor.EBI University of Wisconsin
23713606 116 8-Benzamidochromen-4-one-2-carboxylic acids: potent and selective agonists for the orphan G protein-coupled receptor GPR35.EBI University of Bonn
9435905 180 Three-dimensional quantitative structure-activity relationships from molecular similarity matrices and genetic neural networks. 2. Applications.EBI Harvard University
18077363 314 A systematic interaction map of validated kinase inhibitors with Ser/Thr kinases.EBI University of Oxford
17544277 29 Targeting cytochrome P450 enzymes: a new approach in anti-cancer drug development.EBI University of Maryland
16854069 74 3'-Substituted 7-halogenoindirubins, a new class of cell death inducing agents.EBI Cnrs
21344906 54 Improvement in aqueous solubility in small molecule drug discovery programs by disruption of molecular planarity and symmetry.EBI The University of Tokyo
20060304 9 beta-Naphthoflavone analogs as potent and soluble aryl hydrocarbon receptor agonists: improvement of solubility by disruption of molecular planarity.EBI The University of Tokyo
14684315 1 An electrochemical device for the assay of the interaction between a dioxin receptor and its various ligands.EBI Kyushu University
31952965 2 Synthesis and biological evaluation of FICZ analogues as agonists of aryl hydrocarbon receptor.EBI University of Wisconsin-Madison
31566384 134 Development of Chemical Entities Endowed with Potent Fast-Killing Properties against EBI Glaxosmithkline
31727470 10 Targeting Aryl hydrocarbon receptor for next-generation immunotherapies: Selective modulators (SAhRMs) versus rapidly metabolized ligands (RMAhRLs).EBI University of Perugia
28319389 31 Potential Antiosteoporotic Natural Product Lead Compounds That Inhibit 17?-Hydroxysteroid Dehydrogenase Type 2.EBI University of Basel
28711350 195 Synthesis and biological evaluation of pyrrole-based chalcones as CYP1 enzyme inhibitors, for possible prevention of cancer and overcoming cisplatin resistance.EBI De Montfort University
8666985 12 Similarity between rat brain nicotinic alpha-bungarotoxin receptors and stably expressed alpha-bungarotoxin binding sites.BDB Mcgill University