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Discovery and development of extreme selective inhibitors of the ITD and D835Y mutant FLT3 kinases.
Baska, Ferenc; Sipos, Anna; Orfi, Zoltán; Nemes, Zoltán; Dobos, Judit; Szántai-Kis, Csaba; Szabó, Eszter; Szénási, Gábor; Dézsi, László; Hamar, Péter; Cserepes, Mihály T; Tóvári, József; Garamvölgyi, Rita; Krekó, Marcell; Orfi, László.
Afiliación
  • Baska F; Vichem Chemie Research Ltd, 1022, Budapest, Hungary.
  • Sipos A; Vichem Chemie Research Ltd, 1022, Budapest, Hungary.
  • Orfi Z; Department of Molecular Biology, Max Planck Institute of Biochemistry, 82152, Martinsried, Germany.
  • Nemes Z; Vichem Chemie Research Ltd, 1022, Budapest, Hungary.
  • Dobos J; Vichem Chemie Research Ltd, 1022, Budapest, Hungary.
  • Szántai-Kis C; Vichem Chemie Research Ltd, 1022, Budapest, Hungary.
  • Szabó E; 1st Department of Paediatrics, Semmelweis University, 1083, Budapest, Hungary.
  • Szénási G; Institute of Pathophysiology, Semmelweis University, 1089, Budapest, Hungary.
  • Dézsi L; Institute of Pathophysiology, Semmelweis University, 1089, Budapest, Hungary; Nanomedicine Research and Education Center, Semmelweis University, 1089, Budapest, Hungary.
  • Hamar P; Institute of Pathophysiology, Semmelweis University, 1089, Budapest, Hungary.
  • Cserepes MT; Department of Experimental Pharmacology, National Institute of Oncology, 1122, Budapest, Hungary.
  • Tóvári J; Department of Experimental Pharmacology, National Institute of Oncology, 1122, Budapest, Hungary.
  • Garamvölgyi R; Vichem Chemie Research Ltd, 1022, Budapest, Hungary.
  • Krekó M; Department of Pharmaceutical Chemistry, Semmelweis University, 1085, Budapest, Hungary.
  • Orfi L; Vichem Chemie Research Ltd, 1022, Budapest, Hungary; Department of Pharmaceutical Chemistry, Semmelweis University, 1085, Budapest, Hungary; Drug Research Co, 1161, Budapest, Batthyány u. 92, Hungary. Electronic address: orfi.laszlo@pharma.semmelweis-univ.hu.
Eur J Med Chem ; 184: 111710, 2019 Dec 15.
Article en En | MEDLINE | ID: mdl-31614258
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Pirimidinas / Leucemia Mieloide Aguda / Inhibidores de Proteínas Quinasas / Tirosina Quinasa 3 Similar a fms / Descubrimiento de Drogas / Antineoplásicos Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Eur J Med Chem Año: 2019 Tipo del documento: Article País de afiliación: Hungria
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Pirimidinas / Leucemia Mieloide Aguda / Inhibidores de Proteínas Quinasas / Tirosina Quinasa 3 Similar a fms / Descubrimiento de Drogas / Antineoplásicos Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Eur J Med Chem Año: 2019 Tipo del documento: Article País de afiliación: Hungria