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鞣花酸,一种有前景的药用草药。

Corilagin, a promising medicinal herbal agent.

机构信息

Institute of Chemical Engnieering, Huaqiao University, Xiamen, Fujian 361021, China.

Institute of Chemical Engnieering, Huaqiao University, Xiamen, Fujian 361021, China; Key Laboratory of Xiamen City for Plant Introduction & Quarantine and Plant Product, Xiamen Overseas Chinese Subtropical Plant Introduction Garden, Xiamen, Fujian 361002, China.

出版信息

Biomed Pharmacother. 2018 Mar;99:43-50. doi: 10.1016/j.biopha.2018.01.030. Epub 2018 Jan 8.

Abstract

Corilagin, a gallotannin, is one of the major active components of many ethnopharmacological plants. It was isolated from Caesalpinia coriaria (Jacq.) Willd. (dividivi) by Schmidt in 1951 for the first time. In the past few decades, corilagin was reported to exhibit anti-tumor, anti-inflammatory and hepatoprotective activities, etc. However, little attention was paid to its pharmacological properties due to the complicated and inefficient extract method. In recent years, with the development of extraction technology corilagin was much easier to obtain than before. Thus, people return to pay attention to its anti-tumor, hepatoprotective, and anti-inflammatory activities, particularly as an anti-tumor agent candidate. Our research team had focused on the distribution, preparation and anti-tumor activity of corilagin since 2005. We found corilagin showed good anti-tumor activity on hepatocellular carcinoma and ovarian cancer. What's more, corilagin showed a low level of toxicity toward normal cells and tissues. Due to the extensive attention that corilagin has received, we present a systematic review of the pharmacological effects of corilagin. In this review, we summarized all the pharmacological effects of corilagin with a focus on the molecular mechanism of anti-tumor activity and show you how corilagin affected the signaling pathways of tumor cells as well as its physicochemical properties, distribution and preparation methods.

摘要

鞣花酸是一种没食子单宁,是许多民族药理学植物的主要活性成分之一。它于 1951 年由 Schmidt 首次从金合欢属(Jacq.)Willd.(dividivi)中分离出来。在过去的几十年中,鞣花酸被报道具有抗肿瘤、抗炎和保肝作用等。然而,由于提取方法复杂且效率低下,人们对其药理性质的关注较少。近年来,随着提取技术的发展,鞣花酸比以前更容易获得。因此,人们重新关注其抗肿瘤、保肝和抗炎活性,特别是作为抗肿瘤药物候选物。自 2005 年以来,我们的研究团队一直专注于鞣花酸的分布、制备和抗肿瘤活性。我们发现鞣花酸对肝癌和卵巢癌表现出良好的抗肿瘤活性。此外,鞣花酸对正常细胞和组织的毒性较低。由于鞣花酸受到广泛关注,我们对其药理学作用进行了系统评价。在本次综述中,我们总结了鞣花酸的所有药理学作用,重点介绍了其抗肿瘤活性的分子机制,并向您展示了鞣花酸如何影响肿瘤细胞的信号通路以及其理化性质、分布和制备方法。

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