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The Rhodadyns, a New Class of Small Molecule Inhibitors of Dynamin GTPase Activity.
Robertson, Mark J; Hadzic, Gordana; Ambrus, Joseph; Pomè, D Yuri; Hyde, Emily; Whiting, Ainslie; Mariana, Anna; von Kleist, Lisa; Chau, Ngoc; Haucke, Volker; Robinson, Phillip J; McCluskey, Adam.
Afiliação
  • Robertson MJ; Chemistry, The University of Newcastle , University Drive, Callaghan, NSW 2308, Australia.
  • Hadzic G; Chemistry, The University of Newcastle , University Drive, Callaghan, NSW 2308, Australia.
  • Ambrus J; Chemistry, The University of Newcastle , University Drive, Callaghan, NSW 2308, Australia.
  • Pomè DY; Chemistry, The University of Newcastle , University Drive, Callaghan, NSW 2308, Australia.
  • Hyde E; Chemistry, The University of Newcastle , University Drive, Callaghan, NSW 2308, Australia.
  • Whiting A; Cell Signalling Unit, Children's Medical Research Institute, The University of Sydney , Sydney, NSW 2145, Australia.
  • Mariana A; Cell Signalling Unit, Children's Medical Research Institute, The University of Sydney , Sydney, NSW 2145, Australia.
  • von Kleist L; Leibniz Institut für Molekulare Pharmakologie & Freie Universität Berlin , 13125 Berlin, Germany.
  • Chau N; Cell Signalling Unit, Children's Medical Research Institute, The University of Sydney , Sydney, NSW 2145, Australia.
  • Haucke V; Leibniz Institut für Molekulare Pharmakologie & Freie Universität Berlin , 13125 Berlin, Germany.
  • Robinson PJ; Cell Signalling Unit, Children's Medical Research Institute, The University of Sydney , Sydney, NSW 2145, Australia.
  • McCluskey A; Chemistry, The University of Newcastle , University Drive, Callaghan, NSW 2308, Australia.
ACS Med Chem Lett ; 3(5): 352-6, 2012 May 10.
Article em En | MEDLINE | ID: mdl-24900478
Six focused rhodanine-based libraries, 60 compounds in total, were synthesized and evaluated as potential dynamin I GTPase inhibitors. Twenty-six were more potent than the lead compound with 13 returning IC50 values ≤10 µM, making the Rhodadyn series among the most active dynamin inhibitors reported. Two analogues were highly effective at blocking receptor-mediated endocytosis: C10 and D10 with IC50(RME) = 7.0 ± 2.2 and 5.9 ± 1.0 µM, respectively. These compounds are equipotent with the best reported in-cell dynamin inhibitors.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2012 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2012 Tipo de documento: Article