• Media type: E-Article
  • Title: 8‐Aminoquinolines with an Aminoxyalkyl Side Chain Exert in vitro Dual‐Stage Antiplasmodial Activity
  • Contributor: Leven, Michael; Held, Jana; Duffy, Sandra; Alves Avelar, Leandro A.; Meister, Stephan; Delves, Michael; Plouffe, David; Kuna, Krystina; Tschan, Serena; Avery, Vicky M.; Winzeler, Elizabeth A.; Mordmüller, Benjamin; Kurz, Thomas
  • Published: Wiley, 2019
  • Published in: ChemMedChem, 14 (2019) 4, Seite 501-511
  • Language: English
  • DOI: 10.1002/cmdc.201800691
  • ISSN: 1860-7187; 1860-7179
  • Keywords: Organic Chemistry ; General Pharmacology, Toxicology and Pharmaceutics ; Molecular Medicine ; Drug Discovery ; Biochemistry ; Pharmacology
  • Origination:
  • Footnote:
  • Description: <jats:title>Abstract</jats:title><jats:p>A series of novel 8‐aminoquinolines (8‐AQs) with an aminoxyalkyl side chain were synthesized and evaluated for in vitro antiplasmodial properties against asexual blood stages, liver stages, and sexual stages of <jats:italic>Plasmodium falciparum</jats:italic>. 8‐AQs bearing 2‐alkoxy and 5‐phenoxy substituents on the quinoline ring system were found to be the most promising compounds under study, exhibiting potent blood schizontocidal and moderate tissue schizontocidal in vitro activity.</jats:p>