Comparison of CYP 3A4 metabolism between DA-8159 and Sildenafil in vitro and in vivo

  • Park, Kyung-Jin (Research Laboratories. Dong-A Pharmaceutical Co., Ltd.) ;
  • Youn, Hae-Sun (Research Laboratories. Dong-A Pharmaceutical Co., Ltd.) ;
  • Shim, Hyun-Joo (Research Laboratories. Dong-A Pharmaceutical Co., Ltd.) ;
  • Kim, Soon-Hoe (Research Laboratories. Dong-A Pharmaceutical Co., Ltd.) ;
  • Yoo, Moo-Hi (Research Laboratories. Dong-A Pharmaceutical Co., Ltd.) ;
  • Kim, Won-Bae (Research Laboratories. Dong-A Pharmaceutical Co., Ltd.)
  • 발행 : 2002.10.01

초록

DA-8159 is a new PDEV inhibitor, synthesized by Dong-A Pharm, as an oral agent to treat male erectile dysfunction. DA-8159 and sildenafil are mainly metabolized by cytochrome P450 enzyme CYP 3A4. In this study. we compared the metabolism of DA-8159 with sildenafil in vitro and in vivo. First, we quantified the remaining gatio of original compound, DA-8159 and sidenafil., after we incubated drugs for 30 minutes with human liver microsome cytochrome P 450 3A4. (omitted)

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