Title of article :
Discovery of potent and orally active tricyclic-based FBPase inhibitors Original Research Article
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 ,
Issue Information :
روزنامه با شماره پیاپی سال 2010
Pages :
6
From page :
5346
To page :
5351
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
Journal title :
Bioorganic and Medicinal Chemistry
Serial Year :
2010
Journal title :
Bioorganic and Medicinal Chemistry
Record number :
1306735
Link To Document :
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