刘健

发布者:韩婧发布时间:2025-03-26浏览次数:1379



姓名:刘健

职称:副教授、硕士生导师

E-mailliujian623@njucm.edu.cn

主要研究方向: 药物分子设计与合成


个人简介

药物化学博士,副教授,硕士生导师。2015年博士毕业于复旦大学药物化学专业,同年9月进入南京中医药大学药学院参加工作。目前,已获得国家自然科学基金青年基金、江苏省自然科学基金面上项目及青年基金、江苏省高校自然科学基金面上项目等基金资助,作为第二参与人参加国家自然科学基金--云南联合基金项目,入选江苏省第六期“333”第三层次人才。迄今在J. Med. Chem., Eur. J. Med. Chem., Org. Lett., Adv. Synth. CatalSCI期刊上,以第一作者、通讯作者发表SCI论文30余篇, 授权中国专利3项,澳洲专利1项,其中两项专利已与相关企业达成转让协议,里程碑式付款。担任JMCEJMC等多个学术期刊的审稿人。


承担的主要科研项目

1.南京中医药大学中药学一流学科前沿探索性交叉科学研究项目(ZYXJC2024-007),基于人工智能技术的中药活性成分的物质识别及其成药性优化,主持,20万,在研

22024年南京大学中医研究院中西医协同研究开放课题(ICM2024022),利用GPT生成模型发现新型抗炎药物,主持,4万,在研

3.企业技术转让,炎性小体抑制剂PD-4-26的抗溃疡性结肠炎、痛风研究与开发,参与,在研,里程碑式付款已到账400

4. 国家自然科学基金云南联合基金重点项目(U2102201),强活性、高选择性的NLRP3炎症小体活化抑制剂去氢木香烃内酯的作用机制及其构效关系研究,2022/01-2025/12,参与,233万,在研

5. 江苏省自然科学基金面上项目(BK20211301),新型FGFR4蛋白降解剂的设计、合成及生物活性研究,2021/07-2024/06,主持,10万,在研

6. 国家自然科学基金青年基金项目(81703342),基于氨基酸突变耐药的新兴抑制剂的设计合成机制研究,2018/01-2020/12,主持,20.1万,已结题

7. 江苏省自然科学基金青年基金项目(BK20161050),针对“卡口残基”突变的新型FGFR抑制剂设计、合成及生物活性研究,主持,2016/07-2019/0620万,已结题

8. 江苏省高校自然科学基金面上项目(16KJB350003),新型吲唑类FGFR抑制剂的结构优化及生物活性研究,2016/09-2018/06,主持,3万,已结题


代表性论文10篇以内,需标注共同第一作者或共同通讯作者,论文格式需统一)

  1. Qing-Qing Li #, Xu Quan #, Zi-Xuan Wang #, Nuo Qiao, Xing-Feng Ni, Xiao-Long Jing, Shuang-Shuang Zhou, Xin-Lei Tian, Guo-Chuang Zheng, Kang-Ning Zhan, Yu-Jing Xu, Jin Yang, Yun Zhou, Xiao-Ting Liang, Zong-Hao Zhao, Tian-Hua Wei, Qian Liu, Ming-Yu Bai, Shan-Liang Sun, Yan-Cheng Yu, Peng Cao, Nian-Guang Li *, Xiao-Meng Zhang *, Jian Liu *, Zhi-Hao Shi *. Design, Synthesis, and Biological Evaluation of 3,4-Dihydroisoquinolin-1(2H)-one Derivatives as Protein Arginine Methyltransferase 5 Inhibitors for the Treatment of Non-Hodgkin’s Lymphoma. Journal of Medicinal Chemistry. 2025, 68, 108-134. (中科院一区)

  2. Mengting Li#, Lingyu Ma#, Jiahao Lv#, Zhe zheng, Wenyu Lu, Xunkai Yin, Weijiang Lin, Ping Wang, Jian Cui*, Lihong Hu*, Jian Liu*. Design, synthesis, and biological evaluation of oridonin derivatives as novel NLRP3 inflammasome inhibitors for the treatment of acute lung injury. European Journal of Medicinal Chemistry.2024, 277,116760. (中科院二区)

  3. Rupeng Dai#, Xueting Bao#, Chao Liu#, Xunkai Yin#, Zhenzhen Zhu, Zhe Zheng, Bo Wang, Kundi Yang, Hongmei Wen*, Wei Li*, Haohao Zhu*, Qianming Du*, Jian Liu*. Drug discovery of N-methyl-pyrazole derivatives as potent selective estrogen receptor degrader (SERD) for the treatment of breast cancer. European Journal of Medicinal Chemistry.2024, 279, 116894. (中科院二区)

  4. Lingyu Ma#, Mengting Li#, Jiahao Lv#, Qingxin Yuan, Xunkai Yin, Wenyu Lu, Weijiang Lin, Ping Wang, Jian Cui, Qi Lv*, Jian Liu*, Lihong Hu*. Design, synthesis, and biological evaluation of novel sesquiterpene lactone derivatives as PKM2 activators with potent anti-ulcerative colitis activities. European Journal of Medicinal Chemistry. 2024, 272, 116426. (中科院二区)

  5. Rupeng Dai#, Xueting Bao#, Ying Zhang, Yan Huang, Haohao Zhu*, Kundi Yang, Bo Wang, Hongmei Wen*, Wei Li*, Jian Liu*. Hot-Spot Residue-Based Virtual Screening of Novel Selective Estrogen-Receptor Degraders for Breast Cancer Treatment. Journal Chemical Information and Modeling. 2023, 63, 23, 7588-7602. (中科院二区)

  6. Hui-juan Luo#, Dong-juan Si#, Xin-jie Sun, Meng-yun Wang, Yao-bin Yang, Bo Wang, Hong-mei Wen*, Wei Li*, Jian Liu*. Structure-based discovery of novel α-aminoketone derivatives as dual p53-MDM2/MDMX inhibitors for the treatment of cancer. European Journal of Medicinal Chemistry, 2023, 252, 115282. (中科院二区)

  7. Ping Wang#, Hongqiong Yang#, Weijiang Lin#, Jingxian Zhou, Yi Liu, Lingyu Ma, Mengting Li, Yang Hu, Chengli Yu, Yinan Zhang, Qi Lv *, Jian Liu*, Lihong Hu *. Discovery of Novel Sesquiterpene Lactones Derivatives as Potent PKM2 Activators for the Treatment of Ulcerative Colitis. Journal of Medicinal Chemistry, 2023, 66 (8): 5500-5523. (中科院一区)

  8. Xiaomeng Zhang#, Yazhou Wang#, Jianfeng Ji#, Dongjuan Si, Xueting Bao, Zhuangzhuang Yu, Yueyue Zhu, Liwen Zhao, Wei Li*, Jian Liu*.Discovery of 1,6-Naphthyridin-2(1H)-one Derivatives as Novel, Potent, and Selective FGFR4 Inhibitors for the Treatment of Hepatocellular Carcinoma.Journal of Medicinal Chemistry, 2022 ,65 (11), 7595-7618. (中科院一区)

  9. Xiaomeng Zhang#, Yazhou Wang#, Xue Li, Jie Wu, Liwen Zhao*, Wei Li*, Jian Liu*. Dynamics-Based Discovery of Novel, Potent Benzoic Acid Derivatives as Orally Bioavailable Selective Estrogen Receptor Degraders for ERα+ Breast Cancer. Journal of Medicinal Chemistry, 20216411, 7575-7595. (中科院一区)

  10. Jian Liu *, Jingxian Zhou #, Fengjun He #, Liang Gao, Yu Wen, Lina Gao, Ping Wang, Di Kang *, Lihong Hu*. Design, Synthesis and Biological Evaluation of Novel Indazole-Based Derivatives as potent HDAC Inhibitors via Fragment-Based Virtual Screening. European Journal of Medicinal Chemistry, 2020, 192, 112189. (中科院二区)


其他成果

1.胡立宏; 刘健; 吕祁; 胡杨; 王平; 董董; 杨梦;愈创木烷类倍半萜衍生物及其制药用途,2022-5-25,中国专利授权,ZL202210573181.1

2.胡立宏; 吕祁; 刘健; 胡杨; 王平; 董董; 杨梦;愈创木烷类倍半萜前药及其用途,2022-5-25,中国专利授权,ZL202210574929.X

3HU, Lihong; LIU, Jian; LV, Qi; HU, Yang; DONG, Dong; WANG, Ping; YANG, MengGUAIANE SESQUITERPENE DERIVATIVES AND PHARMACEUTICAL USE THEREOF2022-5-26,澳大利亚专利授权,AU2022282314

4.胡立宏; 吕祁; 刘健; 张毅楠; 胡杨; 王平; 邢瑶 ; 二氢黄酮苷衍生物在制备防治结肠炎的药物中的用途, 2021-2-25, 中国专利授权, 202110210470.0





南中医药学院南中医药学院学子南中医药学院研究生