Author/Authors :
Ayumu Kurimoto، نويسنده , , Tetsuhiro Ogino، نويسنده , , Shinji Ichii، نويسنده , , Yoshiaki Isobe، نويسنده , , Masanori Tobe، نويسنده , , Haruhisa Ogita، نويسنده , , Haruo Takaku، نويسنده , , Hironao Sajiki، نويسنده , , Kosaku Hirota، نويسنده , , Hajime Kawakami، نويسنده ,
Abstract :
Recently, we have reported the 8-hydroxyadenine derivatives (2–4) as a novel class of interferon (IFN) inducing agents. In the present study, a series of 8-hydroxyadenines, which possess various amino moieties at the adenine C(2)-position, were synthesized and evaluated for their ability to induce endogenous IFN in comparison to the known active agent, Imiquimod. Among the compounds prepared, compound 9o possessing a 2-methoxyethylamino group at C(2)-position of adenine was found to exhibit potent IFN inducing activity in vivo. Compound 9o induced IFN from the dosage of 0.1 mg/kg, which was 30-fold potent than that of Imiquimod, and showed a good oral bioavailability (F=81%).