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郭靖

郭靖 助理教授

药物化学

药学院

guojingspu@163.com

深圳大学西丽校区A1-510

1)针对可成药靶点的临床前候选化合物开发​
2)PROTAC/分子胶水降解剂开发与靶标功能探索​

2013年毕业于沈阳药科大学,获学士学位。2018年毕业于沈阳药科大学,获药物化学博士学位。2018-2024年在暨南大学药学院丁克/陆小云教授课题组从事博士后和特聘副研究员研究工作。2025年1月受聘为深圳大学医学部-药学院助理教授,副研究员。主要研究方向为基于靶标的合理性药物设计、合成及活性评价。现主持国家自然科学青年基金项目1项,广东省基础与应用基础研究自然科学基金面上项目2项,广州市科技局-青年博士“启航”项目1项;以第一或共同第一作者在Journal of Medicinal Chemistry European Journal of Medicinal ChemistryBioorganic ChemistryExpert Opinion on Drug Discovery、Expert Opinion on Therapeutic Patents等药物化学国际权威期刊发表论文10篇。

1. 国家自然科学基金青年科学基金项目,选择性ACK1抑制剂的设计、合成及抗肿瘤活性研究,2023.01 - 2025.12,82204182,30万元,主持

2. 广东省基础与应用基础研究基金自然科学基金面上项目,TBK1降解剂的设计、合成及抗肿瘤活性研究,2024.01 - 2026.12,15万元,主持

3. 广东省基础与应用基础研究基金自然科学基金面上项目,3-氨基吲唑类选择性FGFR4共价小分子抑制剂的设计、合成及生物活性研究,2023.01 - 2025.12,10万元,主持

4. 广州市科技局-青年博士“启航”项目, FGFR4大环类共价小分子抑制剂的设计、合成及生物活性研究, 2024.04 - 2026.03, 5 万元,主持

1. Jing Guo1, Haotian Tang1, Wenchao Zhao1, Shukai Song, Fang Feng, Shengjie Huang, Xuan Wang, Yang Zhou, Junping Pei,Dong Guo*,Hua Xie*, Xiaoyun Lu*. Discovery of TBK1 Molecular Glue Degraders as a Potential Strategy for the Treatment of Autosomal Dominant Polycystic Kidney Disease (ADPKD). Journal of Medicinal Chemistry, (in press, 1 co-first author)

2. Jing Guo1, Xiaojuan Chen1, Xiaofei Li, Min Shao, Xiaojuan Song, Lin Zhang, Shengjie Huang, Adam V. Patterson, Jeff B. Smaill,Yang Zhou,Xiangrong Yu*, Yongheng Chen*, Xiaoyun Lu*. Optimization of AminoindazoleDerivatives as Highly Selective Covalent Inhibitors for Wild-Type and MutantFGFR4. Bioorganic chemistry, 160 (2025), 108469. (1 co-first author)

3. Jing Guo1, Shuang Xiang1, Jie Wang1, YangZhou, Zuqin Wang, Zhang Zhang*, Ke Ding*, Xiaoyun Lu*. Discovery of novel TrkA allosteric inhibitors: Structure-based virtual screening, preliminary SAR and the binding mode validation via molecular dynamics simulation. European Journal of Medicinal Chemistry,228 (2022), 114022.

4.Jing Guo, TingtingWang, TianxiaoWu, Kehan Zhang, Wenbo Yin, Mingyue Zhu, Yu Pang, Chenzhou Hao, Zhonggui He, Maosheng Cheng, Yang Liu*, Jiang Zheng, Jingkai Gu*, Dongmei Zhao*. Synthesis, bioconversion, pharmacokinetic and pharmacodynamic evaluation of N-isopropyl-oxy-carbonyloxymethyl prodrugs of CZh-226, a potent and selective PAK4 inhibitor. European Journal of Medicinal Chemistry, 186 (2020), 111878.

5.Jing Guo1, Fan Zhao1, Wenbo Yin, MingyueZhu, Chenzhou Hao, Yu Pang, Tianxiao Wu, Jian Wang, Dongmei Zhao*, Haitao Lib*, Maosheng Cheng*. Design, synthesis, structure-activity relationship study and X-ray crystallography of 3-substituted-indolin-2-one-5-carboxamide derivatives as PAK4 inhibitors. European Journal of Medicinal Chemistry,155 (2018), 197-209. (1 co-first author)

6.Minhao Huang1, Yongjun Huang1,Jing Guo1, Lei Yu, Yu Chang, XiaoluWang, Jinfeng Luo, Yanhui Huang, Zhengchao Tu, Xiaoyun Lu, Yong Xu, Zhimin Zhang*, Zhang Zhang*, Ke Ding*. Pyrido [2, 3-d] pyrimidin-7(8H)-ones as new selective orally bioavailable Threonine Tyrosine Kinase (TTK) inhibitors. European Journal of Medicinal Chemistry, 211 (2021), 113023. (1 co-first author)

7.Jing Guo, Mingyue Zhu, Tianxiao Wu, Chenzhou Hao, Kai Wang, Zizheng Yan, Wanxu Huang, Jian Wang, Dongmei Zhao*, Maosheng Cheng*. Discovery of indolin-2-one derivatives as potent PAK4 inhibitors:Structure-activity relationship analysis, biological evaluationand molecular docking study. Bioorganic & Medicinal Chemistry,25 (2017), 3500 -3511.

8.Jing Guo, Zhen Zhang, Ke Ding*. A patent review of discoidin domain receptor 1 (DDR1) modulators (2014-present), Expert Opinion on Therapeutic Patents, 30 (2020), 341-350.

9.Jing Guo, Yang Zhou, Xiaoyun Lu*. Advances in protein kinase drug discovery through targeting gatekeeper mutations, Expert Opinion on drug discovery, 18 (2023), 1349-1366.

10.Jintong Du1,Jing Guo1, Dongwei Kang1, Zhihong Li1, Guan Wang1, Jianbing Wu1, Zhen Zhang, Hao Fang*, Xuben Hou*, Zhangjian Huang*, Guobo Li*, Xiaoyun Lu*, Xinyong Liu*, Liang Ouyang*, Li Rao*, Peng Zhan*, Xiaojin Zhang*, YihuaZhang*. New techniques and strategies in drug discovery. Chinese Chemical Letters, 31 (2020), 1695-1708. (1 co-first author) 

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