从盆地大矢车菊中分离出的去乙酰基马钱子苷衍生物的合成与生物学评价

N. Paucar, Shanae Van Leuven, Karl De Jesus, Srinath Pashikanti, Sameena Mateen, S. Pradhan, Kavita Sharma
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引用次数: 0

摘要

去乙酰马钱子苷是一种倍半萜内酯(SL),是从盆地大鼠尾草(Artemisia tridentata subsp.)去乙酰马钱子苷的药用价值尚未得到充分开发;因此,本研究是一项探索性研究,旨在评估其作为抗癌特性潜在来源的生物活性。在此,我们采用已报道的方法合成了去乙酰马钱子苷衍生物,并将合成的化合物提交给美国国家癌症研究所(NCI),以检测其抗癌特性。我们之前的研究评估了从盆地大鼠尾草中分离出来的可溶性物质对 NCI-60 癌细胞系筛选的生物活性,拓展了我们对去乙酰马曲卡林的衍生化工作。从盆地大鼠尾草中分离纯化的去乙酰马钱子苷合成的所有化合物都获得了高产率。合成的去乙酰马钱子苷衍生物的结构通过核磁共振实验得到了证实。然后对这些化合物进行了 NCI-60 癌细胞株筛选评估。NCI-60 癌细胞系筛选结果表明,与天然前体相比,一些经化学修饰的去乙酰马曲卡林衍生物在单剂量试验中显示出更强的生物活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and Biological Evaluation of Desacetylmatricarin Derivatives Isolated from Basin Big Sagebrush
Desacetylmatricarin, a sesquiterpene lactone (SL), is the major component extracted from the aerial parts of basin big sagebrush (Artemisia tridentata subsp. tridentata). The medicinal benefits of desacetylmatricarin have not been fully exploited; thus, the current study is an exploratory study to assess its biological activity as a potential source for anti-cancer properties. Herein, we have synthesized desacetylmatricarin derivatives using reported methodologies and examined their anti-cancer properties by submitting the synthesized compounds to the National Cancer Institute (NCI). Our previous studies on the evaluation of the biological activity of the SLs isolated from the basin big sagebrush against the NCI-60 cancer cell line screening expanded our work on derivatizing desacetylmatricarin. All of the compounds synthesized from desacetylmatricarin, which was isolated and purified from the basin big sagebrush, were obtained in high yields. The structures of the synthesized desacetylmatricarin derivatives were confirmed by NMR experiments. These compounds were then evaluated against the NCI-60 cancer cell line screening. NCI-60 cancer cell line screening revealed that some of the chemically modified desacetylmatricarin derivatives showed greater biological activity as compared to the natural precursor in a one-dose assay.
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