Bioorganic & Medicinal Chemistry Letters 2005-07-01

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

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

Index: Bioorg. Med. Chem. Lett. 15 , 3241-6, (2005)

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Abstract

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.

Related Compounds

  • Indole
  • 1-Phenylbutan-1-on...
  • Colchicine
  • Theophylline
  • Phenyl ethyl keton...
  • Acetophenone
  • Valerophenone
  • 8-PHENYLTHEOP...

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