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葫芦素的生物活性及潜在分子靶点:以癌症为重点。

Biological activities and potential molecular targets of cucurbitacins: a focus on cancer.

机构信息

State Key Laboratory of Quality Research in Chinese Medicine, University of Macau, China.

出版信息

Anticancer Drugs. 2012 Sep;23(8):777-87. doi: 10.1097/CAD.0b013e3283541384.

Abstract

Cucurbitacin and its derivatives (cucurbitacins) are a class of highly oxidized tetracyclic triterpenoids. They are widely distributed in the plant kingdom, where they act as heterologous chemical pheromones that protect plants from external biological insults. Their bioactivities first attracted attention in the 1960s. Documented data demonstrate that cucurbitacins possess strong pharmacological properties, such as antitumor, anti-inflammatory, and hepatoprotective effects, etc. Several molecular targets for cucurbitacins have been discovered, such as fibrous-actin, signal transducer and activator of transcription 3, cyclooxygenase-2, etc. The present study summarizes the achievements of the 50 years of research on cucurbitacins. The aim was to systematically analyze their bioactivities with an emphasis on their anticancer effects. Research and development has shed new insight into the beneficial properties of these compounds.

摘要

葫芦素及其衍生物(葫芦素)是一类高度氧化的四环三萜类化合物。它们广泛分布于植物界,作为异源化学信息素,保护植物免受外部生物侵害。它们的生物活性在 20 世纪 60 年代首次引起关注。有文献记载表明,葫芦素具有很强的药理活性,如抗肿瘤、抗炎和保肝作用等。已经发现了葫芦素的几个分子靶点,如纤维状肌动蛋白、信号转导和转录激活因子 3、环氧化酶-2 等。本研究总结了 50 年来对葫芦素的研究成果。目的是系统分析它们的生物活性,重点是它们的抗癌作用。研究和开发为这些化合物的有益特性提供了新的见解。

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