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Lu Zhou
zhoulu@fudan.edu.cn
Chinese, English
Shanghai
Fudan University
Pharmaceutical Sciences
  • 2001.9–2006.7 PhD: Peking University, College of Chemistry and Molecular Engineering
  • 1997.9–2001.7 Bachelor's: Peking University, College of Chemistry and Molecular Engineering
  • Published over 70 research and teaching papers in domestic and international academic journals
  • First author or corresponding author of more than 20 SCI papers
  • Three papers with IF>20 (Cancer Cell 2012, Nature Chemistry 2014, Cell Metabolism 2019)
  • Applied for 6 national invention patents, 4 of which have been authorized
  • Applied for and obtained patent authorizations in the USA, Japan, and other countries and regions
  • 2019.12-Present - Fudan University, School of Pharmacy - Professor
  • 2013.12-2019.11 - Fudan University, School of Pharmacy - Associate Professor
  • 2010.9-2012.7 - University of Chicago, Department of Chemistry - Visiting Scholar
  • 2008.7-2013.11 - Fudan University, School of Pharmacy - Lecturer
  • 2006.7-2008.7 - Peking University, College of Chemistry and Molecular Engineering - Postdoctoral Researcher
  • Shanghai Youth Science and Technology Star Program (2015-2018)
  • Fudan University's First 'Zhuoxue' Program
Drug Chemical Biology
Design and synthesis of small molecule drugs targeting new targets
  • Site-Selective Phosphoglycerate Mutase 1 Acetylation by a Small Molecule, Zhang XD, Jiang, LlL, Huang K, Fang CT, Li J, Yang JT, Li HT, Ruan XX, Wang PH, Mo MG, Wu P, Xu YH, Peng C, Uesugi M, Ye DY, Yu FX, Zhou L, 2020
  • An allosteric PGAM1 inhibitor effectively suppresses pancreatic ductal adenocarcinoma, Wen CL, Huang K, Jiang LL, Lu XX, Dai YT, Shi MM, Tang XM, Wang QB, Zhang XD, Wang PH, Li HT, Ruan XX, Wang LW, Wang XJ, Wang Q, Lu W, Xiang XQ, Sun X, Xu YH, Lai LH, Zhan Q, Li HW, Peng CH, Chen J, Huang JY, Ye DY, Chen SJ, Chen Z, Li M, Fang Y, Shen BY, Zhou L, 2019
  • A Novel Allosteric Inhibitor of Phosphoglycerate Mutase 1 Suppresses Growth and Metastasis of Non-Small-Cell Lung Cancer, Huang K, Liang Q, Zhou Y, Jiang LL, Gu WM, Luo MY, Tang YB, Wang Y, Lu W, Huang M, Zhang SZ, Zhuang GL, Dai Q, Shen QC, Zhang J, Lei HM, Zhu L, Ye DY, Chen HZ, Zhou L, Shen Y, 2019
  • Development of Anthraquinone Analogues as Phosphoglycerate Mutase 1 Inhibitors, Huang K, Jiang L, Li H, Ye D, Zhou L, 2019
  • Synthesis and biological evaluation of anthraquinone derivatives as allosteric phosphoglycerate mutase 1 inhibitors for cancer treatment, Huang K, Jiang L, Liang R, Li H, Ruan X, Shan C, Ye D, Zhou L, 2019
  • Discovery, synthesis and anti-atherosclerotic activities of a novel selective sphingomyelin synthase 2 inhibitor, Li Y, Huang T, Lou B, Ye D, Qi X, Li X, Hu S, Ding T, Chen Y, Cao Y, Mo M, Dong J, Wei M, Chu Y, Li H, Jiang XC, Cheng N, Zhou L, 2019
  • Discovery, cocrystallization and biological evaluation of novel piperidine derivatives as high affinity Ls-AChBP ligands possessing α7 nAChR activities, Yang X, Shen J, Jiang L, Li W, Yu M, Pan G, Yan Y, Zhang C, Jia W, Xiao L, Yu H, Chen H, Zheng Y, Yu L, Xie Q, Zhou L, Shao L, 2018
  • Discovery of 4-Benzyloxybenzo[ d]isoxazole-3-amine Derivatives as Highly Selective and Orally Efficacious Human Sphingomyelin Synthase 2 Inhibitors that Reduce Chronic Inflammation in db/ db Mice, Mo M, Yang J, Jiang XC, Cao Y, Fei J, Chen Y, Qi X, Chu Y, Zhou L, Ye D, 2018
  • The Design and Synthesis of N-Xanthone Benzenesulfonamides as Novel Phosphoglycerate Mutase 1 (PGAM1) Inhibitors, Wang P, Jiang L, Cao Y, Ye D, Zhou L, 2018
  • Xanthone derivatives as phosphoglycerate mutase 1 inhibitors: Design, synthesis, and biological evaluation, Wang P, Jiang L, Cao Y, Zhang X, Chen B, Zhang S, Huang K, Ye D, Zhou L, 2018
  • Conformation and dynamics of the C-terminal region in human phosphoglycerate mutase 1, Liu SE, Hu JC, Zhang H, Xu P, Wan W, Zheng MY, Yu KQ, Ding H, Jiang HL, Zhou L, Luo C, 2017
  • Selective non-zinc binding MMP-2 inhibitors: Novel benzamide Ilomastat analogs with anti-tumor metastasis, Song J, Peng P, Chang J, Liu MM, Yu JM, Zhou L, Sun X, 2016
  • A protein engineered to bind uranyl selectively and with femtomolar affinity, Zhou L, Bosscher M, Zhang C, Ozçubukçu S, Zhang L, Zhang W, Li CJ, Liu J, Jensen MP, Lai L, He C, 2014
  • Tyr26 phosphorylation of PGAM1 provides a metabolic advantage to tumours by stabilizing the active conformation, Hitosugi T, Zhou L, Fan J, Elf S, Zhang L, Xie J, Wang Y, Gu TL, Alečković M, LeRoy G, Kang Y, Kang HB, Seo JH, Shan C, Jin P, Gong W, Lonial S, Arellano ML, Khoury HJ, Chen GZ, Shin DM, Khuri FR, Boggon TJ, Kang S, He C, Chen J, 2013
  • Phosphoglycerate mutase 1 coordinates glycolysis and biosynthesis to promote tumor growth, Hitosugi T, Zhou L, Elf S, Fan J, Kang HB, Seo JH, Shan C, Dai Q, Zhang L, Xie J, Gu TL, Jin P, Alečković M, LeRoy G, Kang Y, Sudderth JA, DeBerardinis RJ, Luan CH, Chen GZ, Muller S, Shin DM, Owonikoko TK, Lonial S, Arellano ML, Khoury HJ, Khuri FR, Lee BH, Ye K, Boggon TJ, Kang S, He C, Chen J, 2012
Drug Design Chemical Biology Small Molecules Cancer Research Pgam1 Inhibitors Hif-1Α Mechanism Study New Drug Targets Synthesis Biological Activity

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