• Medientyp: E-Artikel
  • Titel: The target landscape of clinical kinase drugs
  • Beteiligte: Klaeger, Susan; Heinzlmeir, Stephanie; Wilhelm, Mathias; Polzer, Harald; Vick, Binje; Koenig, Paul-Albert; Reinecke, Maria; Ruprecht, Benjamin; Petzoldt, Svenja; Meng, Chen; Zecha, Jana; Reiter, Katrin; Qiao, Huichao; Helm, Dominic; Koch, Heiner; Schoof, Melanie; Canevari, Giulia; Casale, Elena; Depaolini, Stefania Re; Feuchtinger, Annette; Wu, Zhixiang; Schmidt, Tobias; Rueckert, Lars; Becker, Wilhelm; [...]
  • Erschienen: American Association for the Advancement of Science (AAAS), 2017
  • Erschienen in: Science
  • Sprache: Englisch
  • DOI: 10.1126/science.aan4368
  • ISSN: 0036-8075; 1095-9203
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  • Beschreibung: <jats:title>An atlas for drug interactions</jats:title> <jats:p> Kinase inhibitors are an important class of drugs that block certain enzymes involved in diseases such as cancer and inflammatory disorders. There are hundreds of kinases within the human body, so knowing the kinase “target” of each drug is essential for developing successful treatment strategies. Sometimes clinical trials can fail because drugs bind more than one target. Yet sometimes off-target effects can be beneficial, and drugs can be repurposed for treatment of additional diseases. Klaeger <jats:italic>et al.</jats:italic> performed a comprehensive analysis of 243 kinase inhibitors that are either approved for use or in clinical trials. They provide an open-access resource of target summaries that could help researchers develop better drugs, understand how existing drugs work, and design more effective clinical trials. </jats:p> <jats:p> <jats:italic>Science</jats:italic> , this issue p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" issue="6367" page="eaan4368" related-article-type="in-this-issue" vol="358" xlink:href="10.1126/science.aan4368">eaan4368</jats:related-article> </jats:p>