Li Chang-Wei, Cui Cheng-Bin
State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, Beijing 100850, China.
Molecules. 2014 Dec 19;19(12):21363-77. doi: 10.3390/molecules191221363.
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.
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。