Chemical modification and structure-activity relationships of pyripyropenes; potent, bioavailable inhibitor of acyl-CoA: Cholesterol O-acyltransferase (ACAT)

Rika Obata, Toshiaki Sunazuka, Hiroshi Tomoda, Yoshihiro Harigaya, Satoshi Omura

研究成果: Article査読

31 被引用数 (Scopus)

抄録

Modification and structure-activity relationships of ACAT inhibitor pyripyropene were examined. PR-109 (7g) showed the most potent (IC50 = 6 nM) inhibitory activity. PR-86 (2e) also had strong inhibitory activity (IC50 = 19 nM) and its in vivo activity improved 10 times better (ED50 = 10 mg/kg) than that of pyripyropene A.

本文言語English
ページ(範囲)2683-2688
ページ数6
ジャーナルBioorganic and Medicinal Chemistry Letters
5
22
DOI
出版ステータスPublished - 1995 11 16

ASJC Scopus subject areas

  • 生化学
  • 分子医療
  • 分子生物学
  • 薬科学
  • 創薬
  • 臨床生化学
  • 有機化学

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