首页> 外文OA文献 >Lignans from Schisandra sphenathera Rehd. et Wils. and semisynthetic schisantherin A analogues: Absolute configuration, and their estrogenic and anti-proliferative activity
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Lignans from Schisandra sphenathera Rehd. et Wils. and semisynthetic schisantherin A analogues: Absolute configuration, and their estrogenic and anti-proliferative activity

机译:来自五味子五味子的木质素。 et Wils。和半合成的schisantherin A类似物:绝对构型及其雌激素和抗增殖活性

摘要

A new dibenzocyclooctene-type lignan, named schisandrin A1 (1), together with nine known lignans (2-10), was isolated from the stems of Schisandra sphenathera. The structure of schisandrin A1, which contains a spirocyclic epoxy unit, was established by means of spectroscopic methods. The absolute configurations of schisandrin A1 (1) and schisantherin A (2) were determined by electronic circular dichroism (CD) and TDDFT calculations, with 2 further confirmed by X-ray crystallographic data. Ten new schisantherin A derivatives (11-20) and 6,7-secoschisantherol A (2b) were synthesized. In addition, natural lignans and semisynthetic schisantherin A derivatives showed the antiproliferative activity on four human cancer cell lines and Id1 (an inhibitor of DNA binding protein) and estrogenic potency. Compounds 5, 7, and 8 exhibited very potent estrogenic activity.
机译:从五味子的茎中分离出一种新的二苯并环辛烯型木脂素,称为五味子素A1(1),以及九种已知的木脂素(2-10)。通过光谱方法建立了含五环环氧单元的五味子素A1的结构。五味子素A1(1)和五味子素A(2)的绝对构型通过电子圆二色性(CD)和TDDFT计算确定,其中2个通过X射线晶体学数据进一步证实。合成了十个新的schisantherin A衍生物(11-20)和6,7-secoschisantherol A(2b)。此外,天然木脂素和半合成的schisantherin A衍生物对四种人类癌细胞系和Id1(DNA结合蛋白抑制剂)具有抗增殖活性和雌激素作用。化合物5、7和8表现出非常有效的雌激素活性。

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