4.5 Review

Evodiamine: A Privileged Structure with Broad-ranging Biological Activities

期刊

MINI-REVIEWS IN MEDICINAL CHEMISTRY
卷 22, 期 21, 页码 2680-2701

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1389557522666220404090835

关键词

Evodiamine; alkaloid; natural products; bioactivity; structure-activity relationship; rutaecarpine; beta-carboline

资金

  1. National Natural Science Foundation of China, NSFC [82173716]

向作者/读者索取更多资源

Evodiamine (EVO) is a natural quinolone alkaloid with broad spectrum pharmacological activities, but its moderate activities and poor physicochemical properties limit its clinical application. To seek more potent derivatives, modification of EVO has been extensively conducted. These derivatives exhibit diverse biological activities and act through various mechanisms. However, there is currently no comprehensive review available to systematically summarize the derivatives of EVO.
Evodiamine (EVO) is a natural quinolone alkaloid firstly isolated from the fruit of Evodia rutaecarpa, which is one of the most frequently used traditional Chinese herb for treating a variety of ailments, including headaches, abdominal pain, vomiting, diarrhea, amenorrhea difficult menstruation, postpartum hemorrhage, and other diseases. Latest pharmacological studies showed that EVO possesses a broad spectrum of pharmacological activities through different mechanisms. However, its moderate activities and poor physicochemical properties have hampered its clinical application. In this regard, the modification of EVO aiming at seeking derivatives with more potency and better physicochemical properties has been extensively emerging. These derivatives exhibit diverse biological activities, including antitumor, anti-Alzheimer's disease, anti-pulmonary hypertension, anti-fungi, and thermogenic activities via a variety of mechanisms. Moreover, they are described to act as single, dual, or multiple inhibitors or agonists of many proteins, such as topoisomerase I, topoisomerase II, tubulin, histone deacetylase, sirtuins, butyrylcholinesterase, phosphodiesterase 5, and transient receptor potential vanilloid 1. However, hitherto, there is no comprehensive review to systematically summarize the derivatives of EVO. Considering this perspective, this paper aims to provide a comprehensive description of them by focusing on their diverse biological activities. For each biological activity, the mechanisms and the main structure-activity relationships (SARs) will be presented in cases where adequate information is available. Finally, future directions of this class of compounds will be discussed. This review will be helpful in understanding and encouraging further exploration of EVO.

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