Macías Francisco A, Lacret Rodney, Varela Rosa M, Nogueiras Clara, Molinillo Jose M G
Grupo de Alelopatía, Departamento de Química Orgánica, Facultad de Ciencias, Universidad de Cádiz, C/ República Saharaui s/n, Apdo. 40, 11510-Puerto Real (Cádiz), Spain.
Phytochemistry. 2008 Nov;69(15):2708-15. doi: 10.1016/j.phytochem.2008.08.018. Epub 2008 Oct 1.
The bioactive fractions of Tectona grandis have yielded seven apocarotenoids, two of which have been isolated for the first time as natural products (tectoionols A and B). The chemical structures were determined through 1D and 2D nuclear magnetic resonance experiments. The absolute configuration of tectoionol A was determined using a modified Mosher methodology. Some NMR assignments for the compounds 9(S)-4-oxo-7,8-dihydro-beta-ionol and 3beta-hydroxy-7,8-dihydro-beta-ionone have been corrected on the basis of g-HSQC and g-HMBC experiments. The general bioactivities of isolated compounds have been studied using etiolated wheat coleoptiles. Those compounds that presented higher levels of activity were assayed on standard target species (Lactuca sativa, Lycopersicum esculentum, Lepidium sativum and Allium cepa).
柚木的生物活性成分已产生了七种类胡萝卜素衍生物,其中两种作为天然产物首次被分离出来(柚木醇A和B)。通过一维和二维核磁共振实验确定了化学结构。使用改良的莫舍尔方法确定了柚木醇A的绝对构型。基于g-HSQC和g-HMBC实验对化合物9(S)-4-氧代-7,8-二氢-β-紫罗兰醇和3β-羟基-7,8-二氢-β-紫罗兰酮的一些核磁共振归属进行了校正。使用黄化小麦胚芽鞘研究了分离化合物的一般生物活性。对那些表现出较高活性水平的化合物在标准目标物种(生菜、番茄、独行菜和洋葱)上进行了测定。