Lv Hai-Ning, Wang Shu, Zeng Ke-Wu, Li Jun, Guo Xiao-Yu, Ferreira Daneel, Zjawiony Jordan K, Tu Peng-Fei, Jiang Yong
State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University , Beijing 100191, People's Republic of China.
J Nat Prod. 2015 Feb 27;78(2):279-85. doi: 10.1021/np500861u. Epub 2015 Jan 26.
Two new rare 8-methylbenzo[h]coumarins, muralatins A and B (1, 2), nine new C-8-substituted coumarins, muralatins C-K (3-11), and 22 known analogues (12-33) were isolated from the leaves of Murraya alata. The absolute configurations of compounds 5, 11, 23, 24, 27, 30, and 33 were assigned via comparison of their specific rotations, by Mosher's method, and by single-crystal X-ray diffraction and electronic circular dichroism (ECD) data of the in situ formed transition metal complexes. A putative biosynthesis pathway to 1 and 2 is proposed, and the chemical synthesis of 1 was accomplished through electrocyclization of 5,7-dimethoxy-8-[(Z)-3-methylbut-1,3-dienyl)]coumarin (12). Compounds 1, 2, 8, 12, and 31 showed inhibition of nitric oxide production in lipopolysaccharide-induced RAW 264.7 macrophages with IC50 values of 6.0-14.5 μM.
从翅山小橘的叶子中分离出了两种新的罕见8-甲基苯并[h]香豆素,即翅山小橘素A和B(1, 2),九种新的C-8取代香豆素,翅山小橘素C-K(3-11),以及22种已知类似物(12-33)。通过比较化合物5、11、23、24、27、30和33的比旋光度、采用莫舍尔方法以及利用原位形成的过渡金属配合物的单晶X射线衍射和电子圆二色性(ECD)数据确定了它们的绝对构型。提出了一条通向1和2的推测生物合成途径,并且通过5,7-二甲氧基-8-[(Z)-3-甲基丁-1,3-二烯基)]香豆素(12)的电环化完成了1的化学合成。化合物1、2、8、12和31在脂多糖诱导的RAW 264.7巨噬细胞中显示出对一氧化氮产生的抑制作用,IC50值为6.0-14.5 μM。