摘要
Hispidulin is a naturally occurring flavone known to have various Central nervous system (CNS) activities. Proposed synthetic approaches to synthesizing hispidulin have proven unsatisfactory due to their low feasibility and poor overall yields. To solve these problems, this study developed a novel scheme for synthesizing hispidulin, which had an improved overall yield as well as more concise reaction steps compared to previous methods reported. Additionally, using the same synthetic strategy, d-labelled hispidulin was synthesized to investigate its metabolic stability against human liver microsome. This work may produce new chemical entities for enriching the library of hispidulin-derived compounds.
原文 | 英語 |
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文章編號 | 1897 |
期刊 | Molecules |
卷 | 22 |
發行號 | 11 |
DOIs | |
出版狀態 | 已發佈 - 11月 2017 |
ASJC Scopus subject areas
- 分析化學
- 化學(雜項)
- 分子醫學
- 藥學科學
- 藥物發現
- 物理與理論化學
- 有機化學