Lin Hang, Zhang Wei, Dong Ze-Xi, Gu Ting, Li Nian-Guang, Shi Zhi-Hao, Kai Jun, Qu Cheng, Shang Guan-Xiong, Tang Yu-Ping, Fang Fang, Li He-Min, Yang Jian-Ping, Duan Jin-Ao
National and Local Collaborative Engineering Center of Chinese Medicinal Resources Industrialization and Formulae Innovative Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, Jiangsu, China.
Jiangsu Key Laboratory for High Technology Research of TCM Formulae, Nanjing University of Chinese Medicine, Nanjing 210023, Jiangsu, China.
Int J Mol Sci. 2015 Apr 3;16(4):7587-94. doi: 10.3390/ijms16047587.
Scutellarin (1) has been used for the treatment of angina pectoris, cerebral infarction and coronary heart disease with a large market share in China. Pharmacokinetic studies on scutellarin showed that scutellarin (1) is readily converted into its metabolites in vivo. In this paper, a new and practical synthetic method for the synthesis of 6-O-methyl-scutellarein (3) (one metabolite of scutellarin in vivo) is reported. The benzyl bromide was firstly used to selectively replace the acetyl group at C-7 in 7, and was then used to protect the hydroxy groups at C-4' in 10, 6-O-methyl-scutellarein (3) is obtained in high yield through these methods.
灯盏花素(1)已用于治疗心绞痛、脑梗死和冠心病,在中国占有较大的市场份额。对灯盏花素的药代动力学研究表明,灯盏花素(1)在体内很容易转化为其代谢产物。本文报道了一种合成6-O-甲基灯盏花乙素(3)(灯盏花素在体内的一种代谢产物)的新的实用合成方法。首先用苄基溴选择性取代7中C-7位的乙酰基,然后用于保护10中C-4'位的羟基,通过这些方法以高产率得到6-O-甲基灯盏花乙素(3)。