Artepillin C isoprenomics: Design and synthesis of artepillin C isoprene analogues as lipid peroxidation inhibitor having low mitochondrial toxicity

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• 作者：Yoshihiro Uto ; Shutaro Ae ; Daisuke Koyama ; Mitsutoshi Sakakibara ; Naoki Otomo ; Mamoru Otsuki ; Hideko Nagasawa ; Kenneth L. Kirk and Hitoshi Hori
• 关键词：Artepillin C isoprene analogue ; Isoprenomics ; Lipid peroxidation inhibitor ; Rat liver mitochondria
• 刊名：Bioorganic and Medicinal Chemistry
• 出版年：2006
• 出版时间：15 August 2006
• 年：2006
• 卷：14
• 期：16
• 页码：5721-5728
• 全文大小：195 K

文摘

We designed and synthesized isoprene analogues of artepillin C, a major component of Brazilian propolis, and investigated the inhibitory activity on lipid peroxidation of rat liver mitochondria (RLM) and RLM toxicity based on isoprenomics. We succeeded in the synthesis of artepillin C isoprene analogues using regioselective prenylation within the range from 22 % to 53 % total yield. Reactivity of artepillin C and its isoprene analogues with ABTS (2,2′-Azinobis(3-ethylbenzothiazoline-6-sulfonate)) radical cations showed only a slight difference among the molecules. The isoprene side-chain elongation analogues of artepillin C showed almost the same inhibitory activity against RLM lipid peroxidation as artepillin C. Artepillin C and its isoprene analogues had very weak RLM uncoupling activity. Moreover, artepillin C and its isoprene analogues exhibited a lower inhibitory activity against adenosine 5′-triphosphate (ATP) synthesis by about two orders of magnitude than the effective inhibitory activity against RLM lipid peroxidation. From these results we conclude that artepillin C isoprene analogues could be potent lipid peroxidation inhibitors having low mitochondrial toxicity. We also conclude that elongation of the isoprene side chain of artepillin C to increase lipophilicity had little influence on the inhibitory activity toward RLM lipid peroxidation.