首页|具有酪氨酸酶抑制活性的Broussonin C全合成及其结构简化

具有酪氨酸酶抑制活性的Broussonin C全合成及其结构简化

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Broussonin C是从构树(Broussonetia papyrifera)中分离得到的一种1,3-二芳基丙烷类化合物,具有较好的酪氨酸酶抑制活性.本文以2,4-二羟基苯甲醛为起始原料,经6步反应得到broussonin C,实现其首次全合成.该法操作简单、收率高.同时,在类似物研究中发现,broussonin C无异戊烯基片段的结构类似物酪氨酸酶抑制活性更好,实现了对其结构的有效简化.
Total synthesis of broussonin C with tyrosinase inhibitory activity and its structural simplification
Broussonin C is a 1,3-diarylpropane compound isolated from Broussonetia papyrifera,which has good tyrosinase in-hibitory activity.Using 2,4-dihydroxybenzaldehyde as the starting material,broussonin C has been successfully synthesized in six steps,which achieves the first total synthesis of broussonin C.The method is easy to operate with high yield.Meanwhile,it was found that the compound with non-isopentenyl fragment has better activities,which effectively simplified its structure.

broussonin Ctyrosinase inhibitory activitytotal synthesisstructure simplification

陈慧娟、张兴平、李明明、王扣

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昆明医科大学药学院暨云南省天然药物药理重点实验室

云南中医药大学民族医药学院,昆明 650500

broussonin C 酪氨酸酶抑制活性 全合成 结构简化

云南省中青年学术和技术带头人后备人才项目云南省科技厅-昆明医科大学应用基础研究联合专项

202205AC1600732019FB001-029

2024

天然产物研究与开发
中国科学院成都文献情报中心

天然产物研究与开发

CSTPCD北大核心
影响因子:0.783
ISSN:1001-6880
年,卷(期):2024.36(7)