
姓名:类红瑞
性别:男
籍贯:山东临沂
E-mail:leighongray1023@163.com
职称/职务:特聘教授
所招专业:100701药物化学(硕士)、086002生物与医药(制药工程领域)(硕士)、1055药学(硕士)
通讯地址:辽宁省本溪市溪湖区红柳路85号
办公地点:制药工程学院318办公室(药物化学教研室)
教育经历:
2015.09-2020.06 沈阳药科大学(药物化学,博士)
2011.09-2015.07 沈阳药科大学(基础药学基地班,本科)
工作经历:
2020.08-2022.06 沈阳药科大学师资博士后(博士后)
2022.09-至今 沈阳药科大学制药工程学院教师(药物化学教研室)
社会兼职
1. 辽宁省药学会药物化学专委会委员;
2. 中国老年保健协会创新成果转化与应用评价工作委员会委员;
3. Acta Materia Medica杂志青年编委;
4. 中国药物化学杂志青年编委。
主要研究方向
研究方向一:抗肿瘤及抗纤维化药物小分子的创新性发现、优化与生物活性评价
研究方向二:非专利药物活性成分及活性药物中间体合成工艺改进与优化
研究方向三:基于活性天然产物的结构改造及其降脂活性研究
主持、参与的科研项目(含科研获奖等情况)
1. 具有肝靶向作用的Autotaxin变构抑制剂的发现与抗纤维化研究,82104003,国家自然科学基金委员会青年科学基金项目,30万元,已结题,主持;
2. 特异性ATX-LPA功能轴调节剂的发现及其肿瘤免疫作用探索,项目号2023-BS-111,辽宁省博士启动计划项目,5万元,已结题,主持;
3. 新型共价可逆Autotaxin抑制剂的开发及抗纤维化活性研究,JYTMS20231360,辽宁省教育厅面上项目,3万元,在研,主持;
4. 靶向代谢紊乱与纤维化重大疾病的FXR/泛PPAR双重激动剂的发现,2023MD734179,中国博士后科学基金第73批面上资助,8万元,已结题,主持;
5. 靶向代谢紊乱与纤维化重大疾病的新木姜子碱多样化衍生物的发现,2021M692238,中国博士后科学基金第69批面上资助二等,8万元,已结题,主持;
6. 基于变构调节的靶向DOT1L抑制剂的合理设计、合成及抗肺癌分子机制研究,82173685,国家自然科学基金面上项目,53万元,在研,主要参与者;
7. 基于合成致死策略搭建Core-matched前药共组装体克服肿瘤耐药的机制研究, 82272151,国家自然科学基金面上项目,52万元,在研,主要参与者;
8. 具有抗心肌纤维化作用的ATX抑制剂的发现、优化与作用机制探索研究,81872751,国家自然科学基金面上项目,57万元,已结题,主要参与者;
9. 靶向抗肺纤维化ATX抑制剂LHR-144的研究与开发,2020JH2/10300086,辽宁省2020年度重点研发计划,30万元,已结题,主要参与者;
10. 抗突变耐药的ALK/ROS1双重抑制剂AR-24的研究与开发,CPAYLJ202001,2020年中国药学会-以岭生物医药创新基金资助项目,50万元,在研,主要参与者。
11. 2022年05月 辽宁省教育厅 “辽宁省优秀学位论文(博士)”。
12. 2021年12月 第一届全国博士后创新创业大赛优胜奖(排名5/6)。
发表论文
1. Danping Wang, Shengyao Xu, Si Zheng, Rong Chai, Zhiyu Kuang, Yixin Sun, Yaqi Li, Shiyi Zuo, Xiang Gao, Xin Li, Qikun Jiang, Zhonggui He, Jin Sun, Hongrui Lei*, Anhua Wang*, Bingjun Sun*, Phospholipid-Like Prodrug Liposomes with High Drug-carrier Affinity and High Tumor Selectivity: Strong Competitors of Paclitaxel Nanomedicines, Advanced Functional Materials, 2025, e02341. DOI: 10.1002/adfm.202502341. (中科院一区,IF=19.0).
2. Hongrui Lei, Ming Guo, Xiaopeng Li, Fang Jia, Changtao Li, Yu Yang, Meng Cao, Nan Jiang, Enlong Ma*, Xin Zhai*, Discovery of Novel Indole-based Allosteric Highly Potent ATX Inhibitors with Great in vivo Efficacy in Mouse Lung Fibrosis Model, Journal of Medicinal Chemistry, 2020, 63: 7326-7346. DOI: 10.1021/acs.jmedchem.0c00506. (中科院一区,IF=7.446).
3. Deyi Ma, Zehui Tan, Sen Li, Bing Zhao, Lingfeng Yue, Xiujian Wei, Sha Xu, Nan Jiang, Hongrui Lei*, Xin Zhai*, Discovery of Novel 4,5,6,7-Tetrahydro-7H-pyrazolo[3,4-c]pyridin-7-one Derivatives as Orally Efficacious ATX Allosteric Inhibitors for the Treatment of Pulmonary Fibrosis, Journal of Medicinal Chemistry, 2025, 68, 792−818. DOI: 10.1021/acs.jmedchem.4c02719. (中科院一区,IF=6.9).
4. Deyi Ma, Bing Zhao, Lingfeng Yue, Sen Li, Xiujian Wei, Nan Jiang, Linghe Zang, Hongrui Lei*, Xin Zhai*, Development of Tricyclic 4,5-Dihydro‑3H‑pyrrolo[2,3‑c]quinolin-4-ones as Potent Autotaxin Inhibitors for Pulmonary Fibrosis Treatment In Vivo, Journal of Medicinal Chemistry, 2025, 68, 7476−7498. DOI: 10.1021/acs.jmedchem.4c03173. (IF=6.9).
5. Jiahao Zhang, Sha Xu, Lingfeng Yue, Hongrui Lei*, Xin Zhai*, A Collection of Novel Antitumor Agents That Regulate Lipid Metabolism in the Tumor Microenvironment, Journal of Medicinal Chemistry, 2025, 68, 49−80. DOI: 10.1021/acs.jmedchem.4c02809. (中科院一区,IF=6.9).
6. Hongrui Lei#, Nan Jiang#, Xiuqi Miao, Lingyun Xing, Ming Guo, Yang Liu, Haowen Xu, Ping Gong, Daiying Zuo*, Xin Zhai*, Discovery of Novel Mutant-combating ALK and ROS1 Dual Inhibitors Bearing Imidazolidin-2-one Moiety with Reasonable PK Properties, European Journal of Medicinal Chemistry, 2019, 171, 297-309. DOI: 10.1016/j.ejmech.2019.03.038. (中科院一区,IF=5.573).
7. Hongrui Lei, Changtao Li, Yu Yang, Fang Jia, Ming Guo, Minglin Zhu, Nan Jiang, Xin Zhai*, Structure Guided Design of Potent Indole-based ATX Inhibitors Bearing Hydrazone Moiety with Tumor Suppression Effects, European Journal of Medicinal Chemistry, 2020, 201: 112456. DOI: 10.1016/j.ejmech.2020.112456. (中科院一区,IF=6.504).
8. Hongrui Lei, Zhi Cao, Huinan Wu, Tong Li, Xinyu Wang, Yuxiang Chen, Enlong Ma*, Lixin Sun*, Xin Zhai*, Structural and PK-guided identification of indole-based non-acidic autotaxin (ATX) inhibitors exhibiting high in vivo anti-fibrosis efficacy in rodent model, European Journal of Medicinal Chemistry, 2022, 227: 113951. DOI: 10.1016/j.ejmech.2021.113951. (中科院一区,IF=7.088).
9. Hongrui Lei, Xinyu Wang, Guolong Zhao, Tong Li, Youbao Cui, Huinan Wu, Jing Yang, Nan Jiang, Xin Zhai*, Design, synthesis and promising anti-tumor efficacy of novel imidazo[1,2-a]pyridine derivatives as potent autotaxin allosteric inhibitors, European Journal of Medicinal Chemistry, 2022, 236: 114307. DOI: 10.1016/j.ejmech.2022.114307. (中科院一区,IF=7.088).
10. Deyi Ma, Nan Jiang, Jiachen Zhang, Hongrui Lei*, Xin Zhai*, Development of potent indole-3-carboxamide autotaxin inhibitors with preferred lipophilicity for in vivo treatment of pulmonary fibrosis, European Journal of Medicinal Chemistry, 2025, 288, 117398. DOI: 10.1016/j.ejmech.2025.117398. (中科院一区,IF=6.0).
11. Bing Zhao , Sha Xu , Xiujian Wei , You Li , Shiyi Qu , Hongrui Lei*, Xin Zhai*, Rational design and identification of potent imidazole-fused Autotaxin inhibitors for treatment of idiopathic pulmonary fibrosis, European Journal of Medicinal Chemistry, 2025, 298, 118011. DOI: 10.1016/j.ejmech.2025.118011. (中科院一区,IF=5.9).
12. Lingfeng Yue, Nan Jiang, Xue Fan , Sha Xu, Yuhang Ren, Hongrui Lei*, Xin Zhai*, Rational design and synthesis of 6-(piperazin-1-yl)imidazo[1,2-b]pyridazine derivatives as dual FXR/PPARδ agonists for treatment of pulmonary fibrosis, European Journal of Medicinal Chemistry, 2025, 298, 118013. DOI: 10.1016/j.ejmech.2025.118013. (中科院一区,IF=5.9).
13. Xiujian Wei, Lingfeng Yue, Bing Zhao, Nan Jiang, Hongrui Lei*, Xin Zhai*, Recent advances and challenges of revolutionizing drug-resistant tuberculosis treatment, European Journal of Medicinal Chemistry, 2024, 277,116785. DOI: 10.1016/j.ejmech.2024.116785. (中科院一区,IF=6.0).
14. Bing Zhao, Sha Xu, Shiqing Zhou, Xiangru Jiang, Ailin Jiang, Hongrui Lei*, Xin Zhai*, Research progress on covalent inhibitors targeting alkaline amino acids, Bioorganic Chemistry, 2025, 163, 108800. DOI: 10.1016/j.bioorg.2025.108800. (中科院一区,IF=4.7).
15. Hongrui Lei, Zhen Li, Tong Li, Huinan Wu, Jing Yang, Xinlian Yang, Yu Yang, Nan Jiang, Xin Zhai*, Novel imidazo[1,2-a]pyridine derivatives as potent ATX allosteric inhibitors: Design, synthesis and promising in vivo anti-fibrotic efficacy in mice lung model, Bioorganic Chemistry, 2021, 120: 105590. DOI: 10.1016/j.bioorg.2021.105590. (中科院一区,IF=5.307).
16. Hongrui Lei, Yu Yang, Changtao Li, Fang Jia, Nan Jiang, Ping Gong, Xin Zhai*. Catalyst-free cyclization- and Curtius rearrangement-induced functional group transformation: An Improved Synthetic Strategy of First-in-Class ATX Inhibitor Ziritaxestat (GLPG-1690), Organic Process of Research & Development. 2020, 24(6), 997-1005. DOI: 10.1021/acs.oprd.9b00511. (IF=3.317).
授权专利
1.翟鑫; 类红瑞; 马恩龙; 姜楠; 贾芳; 郭明; 基于吲哚母核的ATX抑制剂及其制备方法和应用,2021-10-26,中国, ZL202010043108.4;
2. 翟鑫; 周宇宏; 宫平; 荆同飞; 类红瑞; 郭明; 邢凌云; 四氢吡啶并[4,3-d]嘧啶类衍生物及其用途,2021-2-26,中国, ZL 201810149223.2;
3.翟鑫; 类红瑞; 谭泽晖; 曹猛; 李通; 一种嘌呤衍生物及其制备方法和用途,2021-3-11,中国,ZL 202110262934.2;
4.翟鑫; 类红瑞; 姜楠; 李通; 一种N-芳基吲哚衍生物及其制备方法和应用,2024-10-01,中国,ZL202310425617.7。