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从南酸枣中分离得到的一种新黄酮类化合物和九种已知黄酮类化合物及其体外抗肿瘤、抗缺氧和抗菌活性

One new and nine known flavonoids from Choerospondias axillaries and their in vitro antitumor, anti-hypoxia and antibacterial activities.

作者信息

Li Chang-Wei, Cui Cheng-Bin

机构信息

State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, Beijing 100850, China.

出版信息

Molecules. 2014 Dec 19;19(12):21363-77. doi: 10.3390/molecules191221363.

Abstract

In the present study, a new flavanoid 1, together with nine known ones 2-10 were isolated from the stem bark of Choerospondias axillaries, the fruit of which was used mainly for treatment of cardiovascular diseases in China. The structure of 1 was established on the basis of its extensive spectral data, and the absolute structures of 1 and 10 were determined by their CD data. The absolute structure of 10 was established for the first time. Among the obtained compounds, 5-8 inhibited the proliferation of K562 cells with inhibition rates of 26.6%, 65.7%, 40.4% and 45.6% at 100 µg/mL; 1 and 4-10 showed significant protective effects on anoxia-induced injury in cultured ECV304 or PC12 cells at 50 µg/mL; 8 and 9 showed antibacterial effects on Staphylococcus aureus ATCC6538 at the tested concentration of 150 µg/8 mm paper disc. Compounds 2 and 4-10 were isolated for the first time from this genus. The proliferation inhibiting activities of 7 and 8, the anti-hypoxia activities of 1 and 4-10, and the antibacterial effect of 8 and 9 on Staphylococcus aureus ATCC6538 are reported here for the first time.

摘要

在本研究中,从南酸枣的茎皮中分离出一种新的黄酮类化合物1以及九种已知化合物2 - 10,在中国其果实主要用于治疗心血管疾病。1的结构基于其广泛的光谱数据确定,1和10的绝对构型通过其圆二色光谱数据确定。10的绝对构型首次得以确定。在所获得的化合物中,5 - 8在100 μg/mL时抑制K562细胞增殖,抑制率分别为26.6%、65.7%、40.4%和45.6%;1以及4 - 10在50 μg/mL时对培养的ECV304或PC12细胞缺氧诱导损伤显示出显著的保护作用;8和9在150 μg/8 mm滤纸片的测试浓度下对金黄色葡萄球菌ATCC6538显示出抗菌作用。化合物2以及4 - 10首次从该属中分离得到。7和8的增殖抑制活性、1以及4 - 10的抗缺氧活性,以及8和9对金黄色葡萄球菌ATCC6538的抗菌作用在此首次报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff6/6271225/87f7ef4e68e5/molecules-19-21363-g001.jpg

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