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个人资料
教育经历2015-09至2020-07,华东师范大学,有机化学,博士 工作经历2023-10至今,华东师范大学,人工智能新药创智中心,副教授 2020-07至2023-09,华东师范大学,博士后(合作导师:吕伟研究员) 个人简介朱书雷,华东师范大学药学院副教授,硕士生导师。目前从事抗肿瘤药物以及衰老疾病药物的设计与递送工作,致力于开发抗肿瘤药物和衰老相关疾病药物应用的新方法和新技术,解决药物脱靶与在靶毒性问题。通过构建新型酶活前药疗法,成功开发出若干新型高效的临床候选药物,已与多个医药公司达成合作,实现科研成果转化。目前,共同设计开发的Linker-Payload平台已应用于包括前药(prodrug)、抗体药物偶联物(ADC)、小分子药物偶联物(SMDC)、多肽药物偶联物(PDC)等体系。基于该平台的抗体药物偶联物,已经获得多个临床批件。另外,有多个候选分子处于临床前研究中。以第一/通讯作者在J. Control. Release, Asian J. Pharm. Sci., J. Med. Chem., Eur. J. Med. Chem.等期刊发表SCI论文20余篇;申请发明专利10项;主持和参与国家自然科学基金青年基金项目1项和企业横向合作项目若干项;担任J. Med.Chem., Eur. J. Med. Chem., Int. J. Nanomed.等期刊审稿人。 社会兼职1)中国药学会会员; 2)中国化学会会员; 3)上海市药学会会员; 课题组科研方向丰富,经费充足,气氛融洽,欢迎报考! 研究方向1. 新型多方式激活药物偶联物 2. 衰老相关疾病新药发现 3. 新型药物递送系统 招生与培养招生专业: 1. 药学学术硕士(药学) 2. 生物与医药工程硕士(制药工程) 开授课程科研项目1. 国家自然科学基金委员会,青年科学基金项目,基于胞外HSP90配体的药物偶联物传递系统,82104000,2020-01至2022-12。 2. 企业合作项目,抗体偶联药物linker-payload研究,2023-12至2024-12。 3. 企业合作项目,ADC毒素-喜树碱类分子联合研究,2022-07至2026-12。 4. 企业合作项目,新型连接子技术联合研究,2024-05至2029-12。 5. 企业合作项目,氘代喜树碱类分子联合研究,2022-12至2030-12。 学术成果代表性成果 1. Zhang, Y. F.; Wang, L.; Cao, X. M.; Song, R. W.; Yin, S. C.; Cheng, Z. Y.; Li, W. N.; Shen, K. Y.; Zhao, T.; Xu, J.; Liu, S. X.; Xie, Q.; Wu, Y. H.; Gao, B.; Guo, Q. S.; Wu, J. S.; Qiu, X. F.; Wang, B. X.; Zhang, W. B.; Yang, T.; Lu, W.; Zhu, S. L.* Evaluation of Double Self-Immolative Linker-Based Antibody–Drug Conjugate FDA022 BB05 with Enhanced Therapeutic Potential. Journal of Medicinal Chemistry, 2024, accepted. 2. Guo, Q. S.; Gao, B.; Song, R. W.; Li, W. N.; Zhu, S. L.; Xie, Q.; Lou, S. S.; Wang, L.; Shen, J. F.; Zhao, T.; Zhang, Y. F.; Wu, J. S.; Lu, W.; Yang, T. FZ-AD005, a Novel DLL3-Targeted Antibody-Drug Conjugate with Topoisomerase I Inhibitor, Shows Potent Antitumor Activity in Preclinical Models. Molecular Cancer Therapeutics, 2024, 23, 1367-1377. 3. Li, Y. L.; Cheng, Z. Y.; Zhou, W.; Wang, L.; Li, X. M.; Xia, G. X.; Lu, W.; Zhu, S. L.* Synthesis and evaluation of homocamptothecin antibody-drug conjugates for cancer treatment. European Journal of Medicinal Chemistry, 2024, 279, 116899. 4. Jiang, X.; Zhu, L. Y.; Wei, Q. Y.; Lu, W.; Yu, J. H.; Zhu, S. L.* Enhancing SN38 prodrug delivery using a self-immolative linker and endogenous albumin transport. Journal of Controlled Release, 2024, 369, 622-629. 5. Lu, Y. X.; Huang, Y., Jin, J. Y.; Yu, J. H.; Lu, W., Zhu, S. L.*. Design, synthesis, and biological evaluation of cathepsin B cleavage albumin-binding SN38 prodrug in breast cancer. Bioorganic Chemistry, 2024, 147, 107370. 6. Cao, Y. T.; Shen, Q. Q.; Ding, M. Y.; Lu, W.; Zhu, S. L.* Development of HSP90 inhibitors-SN38 conjugates for cancer treatment. Bioorganic Chemistry, 2023, 137, 106582. 7. Ding, M. Y.; Zhu, Q. W.; Lu, W.; Zhu, S. L.*. Design and synthesis of multivalent drug delivery system with CA IX inhibitors as ligands. Bioorganic & Medicinal Chemistry, 2023, 93, 117456. 8. Sun, L.; Zhang, J. F.; Zhou, J. E.; Wang, J.; Wang, Z. H.; Luo, Y. Y.; Zhu, S. L.*; Yang, F.; Tang, J.; Lu, W.; Wang, Y. T.; Yu, L.; Yan, Z. Q*. Monitoring the in vivo siRNA release from lipid nanoparticles based on the fluorescence resonance energy transfer principle. Asian Journal of Pharmaceutical Sciences, 2023, 18, 100769. 9. Ding, M. Y.; Shao, Y. Y.; Sun, D. W.; Meng, S. R.; Zang, Y.; Zhou, Y. B.; Li, J.; Lu, W.; Zhu, S. L.* Design, synthesis, and biological evaluation of BRD4 degraders. Bioorganic & Medicinal Chemistry, 2022, 78, 117134. 10. Zhu, S. L.; Liu, J. Y.; Xiao, D. H.; Wang, P. P.; Ma, J. K.; Hu, X. B.; Fu, J. F.; Zhou, Y. B.*; Li, J.*; Lu, W*. Design, synthesis, and biological evaluation of Wee1 kinase degraders. European Journal of Medicinal Chemistry,2022, 243, 114786. 11. Zhu, S. L.; Lu, Y. X.; Jin, J. Y.*; Yu, J. H.; Lu, W*. An HSP90 inhibitor based fluorescent probe for selective tumor targeting. Dyes and Pigments, 2021, 196, 109783. 12. Zhu, S. L.; Li, Y. L.; Huang, Y. S.; Zhang, M. M.; Gu, X. F.; He, Y.; Liu, H. C.; Ma, M. L.*; Lu, W*. Optimized HSP90 mediated fluorescent probes for cancer-specific bioimaging. Journal of Materials Chemistry B, 2020, 8, 1878-1896. 13. Zhu, S. L.; Yu, X. M.; He, Y.; Ma, M. L.*; Lu, W*. Synthesis and fluorescent studies of a low molecular weight rotor for living cancer cell imaging. Dyes and Pigments, 2020, 178, 108353. 14. Zhu, S. L.; Shen, Q. Q.; Gao, Y. L.; Wang, L.; Fang, Y. F.*; Chen, Y.; Lu, W*. Design, synthesis and biological evaluation of HSP90 inhibitor-SN38 conjugates for targeted drug accumulation. Journal of Medicinal Chemistry, 2020, 63, 5421-5441. 15. Zhen, Z.#; Zhu, S. L.#; Jin, J. Y.; Wang, L.*; Lu, W*. A water-soluble probe with p-hydrobenzyl quaternary ammonium linker for selective imaging in senescent cells. Analytica Chimica Acta, 2020, 1133, 99-108. 16. Lu, Y. X.; Sun, D. W.; Xiao, D. H.; Shao, Y. Y.; Su, M. B.; Zhou, Y. B.; Li, J.; Zhu, S. L.*; Lu, W*. Design, synthesis and biological evaluation of HDAC degraders with CRBN E3 ligase ligands. Molecules, 2021, 26, 7241. 17. He, T. T.; Zhu, S. L.*; Lu, W*. Design, synthesis and biological evaluation of 4-(1H-1,2,3-triazol-1-yl)benzamides as HSP90 inhibitors. Molecular Diversity, 2023, 27, 239-248. 18. Ding, M. Y.; Shen, Q. Q.; Lu, W*; Zhu, S. L.*. Synthesis, and biological evaluation of EGFR/HER2-NAMPT conjugates for tumor treatment. Molecular Diversity, 2023, 1-20. 19. Zhang, Y.; Ding, M.; Wang, L.; Yin, S.; Zhang, L.; Cao, X.; Zhu, S. L.*; Yang, T. Synthesis and biological evaluation of novel quaternary ammonium antibody drug conjugates based on camptothecin derivatives. Plos one, 2023, 18(12), e0292871. 20. Huang, Y.; Zhang, W.; Xu, Y. Y.; Zhu, S. L.; Wu, Y. Q.; Chen, T.; Yu, J. Dynamic core crosslinked camptothecin prodrug micelles with reduction sensitivity and boronic acid-mediated enhanced endocytosis: An intelligent tumor-targeted delivery nanoplatform. International Journal of Pharmaceutics, 2020, 580, 119250. 21. Cheng, Z.; Huang, Y.; Shao, P.; Wang, L.; Zhu, S. L.; Yu, J.; Lu, W. Hypoxia-activated albumin-binding exatecan prodrug for cancer therapy. ACS omega, 2021, 7(1), 1082-1089.
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