Towards small molecule inhibitors of mono-ADP-ribosyltransferases.

نویسندگان

  • Torun Ekblad
  • Anders E G Lindgren
  • C David Andersson
  • Rémi Caraballo
  • Ann-Gerd Thorsell
  • Tobias Karlberg
  • Sara Spjut
  • Anna Linusson
  • Herwig Schüler
  • Mikael Elofsson
چکیده

Protein ADP-ribosylation is a post-translational modification involved in DNA repair, protein degradation, transcription regulation, and epigenetic events. Intracellular ADP-ribosylation is catalyzed predominantly by ADP-ribosyltransferases with diphtheria toxin homology (ARTDs). The most prominent member of the ARTD family, poly(ADP-ribose) polymerase-1 (ARTD1/PARP1) has been a target for cancer drug development for decades. Current PARP inhibitors are generally non-selective, and inhibit the mono-ADP-ribosyltransferases with low potency. Here we describe the synthesis of acylated amino benzamides and screening against the mono-ADP-ribosyltransferases ARTD7/PARP15, ARTD8/PARP14, ARTD10/PARP10, and the poly-ADP-ribosyltransferase ARTD1/PARP1. The most potent compound inhibits ARTD10 with sub-micromolar IC50.

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عنوان ژورنال:
  • European journal of medicinal chemistry

دوره 95  شماره 

صفحات  -

تاریخ انتشار 2015