Author/Authors :
Tomoharu Tsukada، نويسنده , , Osamu Kanno، نويسنده , , Takahiro Yamane، نويسنده , , Jun Tanaka، نويسنده , , Taishi Yoshida، نويسنده , , Akira Okuno، نويسنده , , Takeshi Shiiki، نويسنده , , Mizuki Takahashi، نويسنده , , Takahide Nishi، نويسنده ,
Abstract :
With the aim of exploring the effect of tricyclic-based FBPase inhibitors in cells and in vivo, a series of prodrugs of tricyclic phosphonates was designed and synthesized. Introducing prodrug moieties into tricyclic-based phosphonates led to the discovery of prodrug 15c, which strongly inhibited glucose production in monkey hepatocytes. Furthermore, prodrug 15c lowered blood glucose levels in fasted cynomolgus monkeys.
Keywords :
PET deoxygenation , Galactofuranosidase inhibition , 5-Deoxy-d-galactofuranosides , Galactofuranosidase substrates