Synthesis of selective SRPK-1 inhibitors: novel tricyclic quinoxaline derivatives.

نویسندگان

  • Zsolt Székelyhidi
  • János Pató
  • Frigyes Wáczek
  • Péter Bánhegyi
  • Bálint Hegymegi-Barakonyi
  • Dániel Erös
  • György Mészáros
  • Ferenc Hollósy
  • Doris Hafenbradl
  • Sabine Obert
  • Bert Klebl
  • György Kéri
  • László Orfi
چکیده

SR protein-specific kinase-1 (SRPK-1) has been identified as a validated target for hepatitis B virus (HBV). A series of novel tricyclic quinoxaline derivatives was designed and synthesised as potential kinase inhibitory antiviral agents and was found to be active and selective for SRPK-1 kinase. Most of these novel compounds have drug-like properties according to experimentally determined LogP and LogS values.

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عنوان ژورنال:
  • Bioorganic & medicinal chemistry letters

دوره 15 13  شماره 

صفحات  -

تاریخ انتشار 2005