Medina Sonia, Gil-Izquierdo Ángel, Durand Thierry, Ferreres Federico, Domínguez-Perles Raúl
CQM-Centro de Química da Madeira, Universidade da Madeira, Campus da Penteada, 9020-105 Funchal, Portugal.
Research Group on Quality, Safety and Bioactivity of Plant Foods, Department of Food Science and Technology, CEBAS (CSIC), Campus University Espinardo, 30100 Murcia, Spain.
Antioxidants (Basel). 2018 Nov 16;7(11):165. doi: 10.3390/antiox7110165.
Structure-activity relationship (SAR) constitutes a crucial topic to discover new bioactive molecules. This approach initiates with the comparison of a target candidate with a molecule or a collection of molecules and their attributed biological functions to shed some light in the details of one or more SARs and subsequently using that information to outline valuable application of the newly identified compounds. Thus, while the empiric knowledge of medicinal chemistry is critical to these tasks, the results retrieved upon dedicated experimental demonstration retrieved resorting to modern high throughput analytical approaches and techniques allow to overwhelm the constraints adduced so far to the successful accomplishment of such tasks. Therefore, the present work reviews critically the evidences reported to date on the occurrence of phytoprostanes and phytofurans in plant foods, and the information available on their bioavailability and biological activity, shedding some light on the expectation waken up due to their structural similarities with prostanoids and isoprostanes.
构效关系(SAR)是发现新生物活性分子的关键课题。这种方法首先将目标候选物与一种分子或一组分子及其赋予的生物学功能进行比较,以揭示一个或多个构效关系的细节,随后利用这些信息概述新鉴定化合物的有价值应用。因此,虽然药物化学的经验知识对这些任务至关重要,但借助现代高通量分析方法和技术通过专门的实验证明获得的结果能够克服迄今为止对成功完成此类任务所带来的限制。因此,本工作批判性地综述了迄今为止报道的关于植物性前列腺素和植物呋喃在植物性食物中的存在证据,以及关于它们的生物利用度和生物活性的现有信息,揭示了由于它们与前列腺素和异前列腺素的结构相似性而引发的期望。