杜永丽
职称:教授、硕士研究生导师
齐鲁工业大学创新药物研究与开发中心主任
Email: yldu2016@163.com
教育背景:
1995-1999 山东师范大学化学系 化学教育 学士
2003-2008 中国科学院上海药物研究所 药物化学 博士
研究工作经历:
2008-2009 上海睿智化学有限公司 从事国际合作的创新药物研究开发工作
2010上半年 齐鲁制药有限公司 从事创新药物研究开发工作
2010.7-至今 齐鲁工业大学beat365正版唯一官网 从事教学与科学研究工作
研究方向:主要针对非小细胞肺癌、乳腺癌等恶性肿瘤进行靶向创新药物的研究与开发。重点进行创新药物先导化合物的发现与优化、计算机辅助药物设计、生物活性评价环节的研究开发工作。
代表性学术成果:
主持纵向项目:
1、国家自然科学基金,青年基金,批准号81202389,项目名称“新型选择性、功能活性PTP1B抑制剂的设计、合成及生物活性研究”,2013.01-2015.12。
2、国家自然科学基金,面上项目,批准号81872744,项目名称“新型ERR-alpha小分子反向激动剂的设计、合成及抗乳腺癌活性研究”,2019.01-2022.12。
3、山东省自然科学基金,面上项目,批准号ZR2019MH046, 2019.07-2022.06。
代表性论文及专利:
(1)Yongli Du*, Yanhui Zhang , Hao Ling , Qunyi Li, Jingkang Shen, Discovery of novel high potent and cellular active ADC type PTP1B inhibitors with selectivity over TCPTP via modification interacting with C site,European Journal of Medicinal Chemistry,2018,144,692-700, SCI.
(2)Yanhui zhang, Yongli Du*, The development of protein tyrosine phosphate- ase1B inhibitors defined by binding sites in crystalline complexes. Future Medicinal Chemistry 2018,10 (19 ), 2345-2367, SCI.
(3)Rui li, Yongli Du*, Zhipei Gao, Jingkang Shen, Molecular Modeling Studies on Carbazole Carboxamide Based BTK Inhibitors Using Docking and Structure-Based 3D-QSAR. International journal of molecular sciences 2018,19 (4). 1244, SCI.
(4)Rui li, Yongli Du*, Jingkang Shen, Molecular modelling studies on cinnoline -based BTK inhibitors using docking and structure-based 3D-QSAR. SAR and QSAR in environmental research 2018, 29 (11), 847-873, SCI.
(5)Yongli Du*, Lianhua Song, etc. The discovery of novel, potent ERR-alpha inverse agonists for the treatment of triple negative breast cancer.European Journal of Medicinal Chemistry, 2017,136: 457-467, SCI.
(6)Yang Ning, Haifei Chen, Yongli Du*, etc. A novel compound LingH2-10 inhibits the growth of triple negative breast cancer cells in vitro and in vivo as a selective inverse agonist of estrogen-related receptor α. Biomedicine & Pharmacotherapy. 93, 2017, 913–922, SCI.
(7)Haixing Guan, Yongli Du*, etc. A brief perspective of drug resistance toward EGFR inhibitors: the crystal structures of EGFRs and their variants. Future Medicinal Chemistry, 2017, 693-704, SCI.
(8)Haixing Guan, Yongli Du*, etc. Development of Selective Cyclin-Dependent Kinase 4 Inhibitors for Antineoplastic Therapies. Anticancer Agents in Medicinal Chemistry. 2017, 17(5): 646-657,SCI.
(9)Weiwei Han, Yongli Du*, Recent Development of the Second and Third Generation Irreversible Epidermal Growth Factor Receptor Inhibitors. Chemistry & Biodiversity. 2017, 14(7), SCI.
(10)Peihong Liu, Yongli Du*, Lianhua Song, Jingkang Shen, Qunyi Li, Discovery of novel, high potent, ABC type PTP1B inhibitors with TCPTP selectivity and cellular activity, European Journal of Medicinal Chemistry, 2016, 118:27-33, SCI.
(11)Liudi Zhang, Peihong Liu, Haifei Chen, Qunyi Li, Lu Chen, Huijie Qi, Xiaojin Shi, Yongli Du*. Characterization of a selective inverse agonist for estrogen related receptor α as apotential agent for breast cancer. European Journal of Pharmacology. 789, 2016, 439-448,SCI.
(12)Yongli Du*, Hao Ling, Meng Zhang, Jingkang Shen, Qunyi Li, Discovery of novel, potent, selective and cellular active ADC type PTP1B inhibitors via fragment–docking-oriented de novel design, Bioorganic & Medicinal Chemistry, 2015,23: 4891 -4898, SCI.
(13)Peihong Liu, Yongli Du*, Lianhua Song, Jingkang Shen, Qunyi Li, Novel, potent, selective and cellular active ABC type PTP1B inhibitors containing (methane -sulfonyl-phenyl-amino)-acetic acid methyl ester phosphotyrosine mimetic,Bioorganic & Medicinal Chemistry, 2015, 23: 7079 -7088, SCI.
(14)Yongli Du, Qunli Li, Bing Xiong, Xin Hui, Xin Wang, Yang Feng, Tao Meng, Dingyu Hu, Datong Zhang, Mingwei Wang, Jingkang Shen, Aromatic β-amino-ketone derivatives as novel selective non-steroidal progesterone receptor antagonists. Bioorganic & Medicinal Chemistry 2010, 18 (12), 4255- 4268,SCI.
(15)Yongli Du, Qunyi Li, Bing Xiong, Xin Wang, Tao Meng, Dingyu Hu, Mingwei Wang, Jingkang Shen, The Discovery of Novel Non-steroidal Progesterone Receptor Antagonists. Abstract and poster on The 6th International Symposium for Chinese MedicinalChemists. 07. 2008.
(16)2008年07月于第六届世界华人药物化学会议上获奖:The presentation of Yongli Du, Qunyi Li et al entitled The Discovery of Novel Non-steroidal Progesterone Receptor Antagonists has achieved Poster Presentation Award of The 6th International Symposium for Chinese Medicinal Chemists.
(17)杜永丽,李群益,沈竞康,刘培红,新型取代磺酰胺类化合物、制备方法及其作为PTP1B抑制剂的用途,中国专利,CN2015104122426。
(18)杜永丽,沈竞康,李群益,凌浩,新型脲类蛋白酪氨酸磷酸酯酶1B抑制剂及其制备方法、药物组合物和用途,中国专利,CN2015102588258。
(19)杜永丽,沈竞康,李群益,刘培红,新型磺酰胺类化合物、制备方法及其作为蛋白酪氨酸磷酸酯酶1B抑制剂的用途,中国专利,CN2015104140693。
本科生教学:主讲药物化学、新药信息与文献检索等课程。