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任素梅

编辑:付瀚方    时间:2024-04-10    点击数:

95E9        职称:讲师

        邮箱rensumei@zzu.edu.cn

        地址:大学路40号博士后楼116室

 






个人简介

2009年6月在郑州大学药学院获学士学位;2012年6月在复旦大学药学院获硕士学位;2012年7月-2015年8月在复旦大学药学院从事科研助理工作;2019年1月在复旦大学药学院获博士学位;2019年4月至2022年3月,在深圳大学医学部从事博士后研究;2022年7月入职郑州大学医学科学院。



主要研究方向

Toll样受体7激动剂的合成及其在生物免疫治疗中的应用;免疫靶向偶联物的合成及生物活性研究


 

 

代表性成果

1.Sumei Ren, Junbiao Chang, Ruiqi Liu*, Guangyi Jin*. The novel selective TLR7 agonist GY101 suppresses colon cancer growth by stimulating immune cells. Eur J Pharmacol. 2024, 967:176383.

2.Weizhao Weng, Sumei Ren, Changcai Teng, Jia Guo, Qiuyu Guo, Wei Zhang, Chengli Zong*, Ning Ding*. Chemoenzymatic synthesis and immunological evaluation of sialyl-Thomsen-Friedenreich (sTF) antigen conjugate to CRM197. Bioorg Med Chem. 2024, 100:117615.

3.Sumei Ren, Xiaodong Wang*, Guangyi Jin*. Conjugate of ibrutinib with a TLR7 agonist suppresses melanoma progression and enhances antitumor immunity. Int J Biol Sci. 2022, 18(1): 166−179.

4.Sumei Ren, Xiaodong Wang, Jun Song, Guangyi Jin*. Discovery of novel ibrutinib analogues to treat malignant melanoma. Bioorg Chem. 2021, 117: 105419.

5.Sumei Ren, Minmin Zhang, Yujie Wang, Jia Guo, Junfei Wang, Yingxia Li, Ning Ding*. Synthesis and biological evaluation of novel cabazitaxel analogues. Bioorg Med Chem. 2021, 41:116224.

6.Sumei Ren, Ruiqi Liu, Yujie Wang, Ning Ding*, Yingxia Li*. Synthesis and Biological Evaluation of Ginsenoside Compound K Analogues as a Novel Class of Anti-asthmatic Agents. Bioorg Med Chem Lett. 2019, 59:51−55.

7.Sumei Ren, Yujie Wang, Junfei Wang, Dingding Gao, Minmin Zhang, Ning Ding* , Yingxia Li**. Synthesis and biological evaluation of novel larotaxel analogues. Eur J Med Chem. 2018, 156:692−710.

8.Xianglai Liu, Sumei Ren, Qi Gao, Chun Hu*, Yingxia Li, and Ning Ding*. Glycosylation of a Ketone with an O‑Glycosyl Trichloroacetimidate Provides an Enol Glycoside. Org Lett. 2018, 20:5186−5189.

9.Sumei Ren, Qing Chen, Ning Ding, Wei Zhang, Ying Guo*, Yingxia Li*. Synthesis and biological evaluation of analogues of methyl ursolate 3-O-β-chacotrioside as H5N1 viral entry inhibitors. J Carbohydr Chem. 2012, 31:647–658.