a UoN Chair of Oman's Medicinal Plants and Marine Natural Products , University of Nizwa , Nizwa , Sultanate of Oman.
b Center for Marine Biotechnology and Biomedicine , Scripps Institution of Oceanography, University of California , San Diego , La Jolla, CA, 92093-0204, USA.
Expert Opin Ther Pat. 2017 Oct;27(10):1111-1121. doi: 10.1080/13543776.2017.1339792. Epub 2017 Jun 14.
Lapachol (1), β-lapachone (2) and α-lapachone (3) are three well-studied natural products isolated from Tabebuia impetiginosa having most interesting chemodiversity and demonstrating diverse biological effects. Areas covered: The current review summarizes the recent and past discovery of chemotherapeutic agents based on the compounds 1-3. This review presents an overview of patents filed over the past two decades (1997 to 2016) mostly relating to the anticancer effects of these lapachol and lapachone analogues. Expert opinion: The large number of interesting patents published on the therapeutic potential of quinones 1-3 and their synthetic derivatives lends credence to the importance of these molecules. Moreover, these quinones demonstrated potent anticancer effects towards various cancer cell lines and chemical modification of these quinones have led to products displaying enhanced anticancer effects. It is noteworthy that the majority of patents published are on the anticancer effects of quinones 1-3 and their synthetic derivatives along with a limited number of additional biological effects. It is our opinion that in order to get lead compounds, there needs to be a greater focus on the elucidation of the precise mechanism of action of these compounds including SAR and in vivo studies.
拉帕醌(1)、β-拉帕醌(2)和α-拉帕醌(3)是从 Tabebuia impetiginosa 中分离得到的三种研究较为深入的天然产物,具有丰富的化学多样性,并表现出多种生物学效应。
本文综述了基于化合物 1-3 的新型化疗药物的最新和过去的发现。本综述介绍了过去二十年(1997 年至 2016 年)提交的专利申请的概述,这些专利主要涉及这些拉帕醌和拉帕酮类似物的抗癌作用。
大量关于醌 1-3 及其合成衍生物治疗潜力的有趣专利的发表,证明了这些分子的重要性。此外,这些醌类化合物对各种癌细胞系表现出强烈的抗癌作用,对这些醌类化合物的化学修饰导致了具有增强抗癌作用的产物。值得注意的是,发表的大多数专利都集中在醌 1-3 及其合成衍生物的抗癌作用以及有限数量的其他生物学效应上。我们认为,为了获得先导化合物,需要更加关注这些化合物的作用机制的阐明,包括 SAR 和体内研究。