应用天然产物 ›› 2018, Vol. 8 ›› Issue (6): 453-456.DOI: 10.1007/s13659-018-0173-y
• SHORT COMMUNICATION • 上一篇
Cheng-Ji Li1,3, Fan Xia1,3, Rong Wu2, Hong-Sheng Tan2, Hong-Xi Xu2, Gang Xu1, Hong-Bo Qin1
收稿日期:
2018-05-13
修回日期:
2018-06-08
出版日期:
2018-12-24
发布日期:
2018-11-21
通讯作者:
Hong-Xi Xu, Gang Xu, Hong-Bo Qin
基金资助:
Cheng-Ji Li1,3, Fan Xia1,3, Rong Wu2, Hong-Sheng Tan2, Hong-Xi Xu2, Gang Xu1, Hong-Bo Qin1
Received:
2018-05-13
Revised:
2018-06-08
Online:
2018-12-24
Published:
2018-11-21
Contact:
Hong-Xi Xu, Gang Xu, Hong-Bo Qin
Supported by:
摘要: Carnosic acid was used as starting material to synthesize royleanone derivatives featured C11-C14 para quinone. The importance of C-20 group of royleanone derivatives was verified by the cytotoxicity assay of royleanonic acid, miltionone I and deoxyneocrptotanshinone. Following our synthetic route, 15 amide derivatives were synthesized and 8 compounds exhibited moderate cytotoxic activities against three human cancer lines in vitro.
Cheng-Ji Li, Fan Xia, Rong Wu, Hong-Sheng Tan, Hong-Xi Xu, Gang Xu, Hong-Bo Qin. Synthesis and Cytotoxicities of Royleanone Derivatives[J]. 应用天然产物, 2018, 8(6): 453-456.
Cheng-Ji Li, Fan Xia, Rong Wu, Hong-Sheng Tan, Hong-Xi Xu, Gang Xu, Hong-Bo Qin. Synthesis and Cytotoxicities of Royleanone Derivatives[J]. Natural Products and Bioprospecting, 2018, 8(6): 453-456.
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