Chinese Journal of Organic Chemistry ›› 2023, Vol. 43 ›› Issue (2): 646-659.DOI: 10.6023/cjoc202207033 Previous Articles     Next Articles

济源冬凌草甲素衍生物作为潜在抗肿瘤药物的合成及药理学活性研究

王妮a,b, 郑姿君a,b, 贾小苹a,b, 赵梦圆a,b, 王亚蕾a,b, 周臣a,b, 王志佳a,b, 肖泽霖c, 刘宏民a,b,*(), 可钰a,b,*()   

  1. a 郑州大学药物研究院 药物关键制备技术教育部重点实验室 郑州 450001
    b 省部共建食管癌防治国家重点实验室 郑州 450001
    c 广州新华学院健康学院 广州 510310
  • 收稿日期:2022-07-03 修回日期:2022-10-23 发布日期:2022-11-07
  • 基金资助:
    国家自然科学基金(U1904163); 河南省重点研究计划(161100311000)

Study on Synthesis and Pharmacological Research of Jiyuan Oridonin A Derivatives as Potential Anti-tumor Drugs

Ni Wanga,b, Zijun Zhenga,b, Xiaoping Jiaa,b, Mengyuan Zhaoa,b, Yalei Wanga,b, Chen Zhoua,b, Zhijia Wanga,b, Zelin Xiaoc, Hongmin Liua,b(), Yu Kea,b()   

  1. a Key Laboratory of Advanced Drug Preparation Technologies, Ministry of Education, School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001
    b State Key Laboratory of Esophageal Cancer Prevention & Treatment, Zhengzhou 450001
    c School of Health Sciences, Guangzhou Xinhua College, Guangzhou 510310
  • Received:2022-07-03 Revised:2022-10-23 Published:2022-11-07
  • Contact: *E-mail: ky@zzu.edu.cn;liuhm@zzu.edu.cn
  • Supported by:
    National Natural Sciences Foundations of China(U1904163); Key Research Program of Henan Province(161100311000)

Jiyuan oridonin A (JOA), a diterpenoid ingredient purified from Isodon rubescens collected in Jiyuan, Henan Province, exhibited a variety of anti-tumor activities. In order to further develop the medicinal potency of JOA, a series of its 14-OH benzoate derivatives were designed and synthesized, and then their anti-proliferative activities in vitro were evaluated. The results turned out that the anti-tumor activities of this series of derivatives had been improved compared with the those of JOA, and were much better than that of oridonin. Among them, 7α,20-olide-ent-kaur-16-en-11,15-dione-14β-yl 2-nitro-5- chlorobenzoate (OJW8-9) showed the best activity (IC50=(0.478±0.109) μmol/L on SW-1990 cells). Further studies revealed that compound OJW8-9 inhibited the proliferation of SW-1990 cells by blocking cell cycle in the G2/M phase in a time- and concentration-dependent, and might induce apoptosis through reactive oxygen species (ROS) pathway.

Key words: ent-kaurene diterpene, Jiyuan oridonin A (JOA), anti-proliferative activity, reactive oxygen species (ROS) pathway