CH

HE QiuqinMedicinal Chemistry, Associate Professor

E-mail: qqhe@fudan.edu.cn
Office Location: Room A7019, Chemistry Building, Department of Chemistry, Fudan University 2005 Songhu Road, Yangpu District, Shanghai 200438, China
Tel: 86-21-3124

  • Research Interests

  • Academic Appointments

  • Prizes and awards

  • Biography

  • Teaching

  • Key Publications

  • Small molecule drugs R & D

  • New methodologies for synthetic drugs


  • The Second prize for progress in science and technology of Shanghai (2013)

  • 2012.09-now         Department of Chemistry, Fudan University, Lecturer

  • 2009.10-2012.09   Department of Chemistry, Fudan University, Post-doctor

  • 2007.06-2009.10   Shanghai Chempartner Co. Ltd., Team Leader

  • 2002.09-2007.06   Second Military Medical University, Ph.D

  • 1998.09-2002.06   China Pharmaceutical University, Bachelor degree

  • Medicinal Chemistry

  • Experiment of synthetic chemistry

  1. Hai-Qiu Wu, Christophe Pannecouque, Zi-Hong Yan, Wen-Xue Chen, Qiu-Qin He*, Fen-Er Chen,* Jan Balzarini, Dirk Daelemans and Erik De Clercq. Synthesis and biological evaluation of new conformationally restricted S-DABO hybrids as non-nucleoside inhibitors of HIV-1 reverse transcriptase. Med. Chem. Commun.,5 (2014) 468–473.

  2. Zi-Hong Yan, Xia-Yun Huang, Hai-Qiu Wu, Wen-Xue Chen, Qiu-Qin He*, Fen-Er Chen, Erik De Clercq, Christophe Pannecouque. Structural modifications of CH(OH)-DAPYs as new HIV-1 non-nucleoside reverse transcriptase inhibitors. Bioorg. Med. Chem., 22 (2014) 2535–2541.

  3. Le-Meng Hu, Fang-Jun Xiong, Xiao-Fei Chen, Wen-Xue Chen, Qiu-Qin He*, Fen-Er Chen*. Synthetic studies on statins. Part 1: a short and cyanide-free synthesis of atorvastatin calcium via an enantioselective aldol strategy. Tetrahedron: Asymmetry 24 (2013) 207–211.

  4. Shuang-Xi Gu, Zhi-Ming Li, Qiu-Qin He*, Fen-Er Chen*, Erik De Clercq, Jan Balzarini, Christophe Pannecouque. Chiral resolution, absolute configuration assignment and biological activity of racemic diarylpyrimidine CH(OH)-DAPY as potent nonnucleoside HIV-1 reverse transcriptase inhibitors. Eur. J. Med. Chem., 53 (2012), 229-234.

  5. Qiu-Qin He, Shuang-Xi Gu, Jia Liu, Hai-Qiu Wu, Xuan Zhang, Liu-Meng Yang, Yong-Tang Zheng, Fen-Er Chen*. Structural modifications of quinolone-3-carboxylic acids with anti-HIV activity. Bioorg. Med. Chem., 19 (2011), 5039-5045.

Address: Chemistry Building, Department of Chemistry, Fudan University
2005 Songhu Road, Yangpu District, Shanghai 200438, China  Tel: 86-21-31242791
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