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教育背景
1992年毕业于东北师范大学化学系,获学士学位;1995年毕业于东北师范大学有机化学专业,获硕士学位;1998年毕业于中国医学科学院,中国协和医科大学药物研究所药物化学专业,获博士学位。
工作经历
1998年9月至2000年10月工作于药物研究所,任助理研究员。2000年11月到美国加洲大学戴维斯癌症研究中心做博士后,从事固相组合化学研究。2002年3月到弗吉尼亚理工大学做博士后,从事肽模拟物的设计与合成工作。2004年2月回到药物所工作,先后任助理研究员、副研究员和研究员。
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支持扩展名:.rar .zip .doc .docx .pdf .jpg .png .jpeg1. PARP抑制剂的设计、合成和抗肿瘤活性研究
2. FBPase抑制剂的设计、合成和抗糖尿病药物研究
3. Pin1小分子抑制剂的设计、合成及生物功能研究
4. 靶向钾离子通道Kv2.1选择性阻断剂的设计、合成及生物功能研究
1.Lifei Du, Xiaoyu Wang, Guonan Cui, Bailing Xu* Design, synthesis and biological evaluation of novel thiazole-based derivatives as human Pin1 inhibitors, Bioorganic & Medicinal Chemistry, 2021, 29: 115878
2.Jie Zhou#, Jianbo Bie#, Xiaoyu Wang#, Quan Liu, Rongcui Li, Hualong Chen, Jinping Hu, Hui Cao, Wenming Ji, Yan Li, Shuainan Liu*, Zhufang Shen*, Bailing Xu*Discovery of N-arylsulfonyl-indole-2-carboxamide Derivatives as Potent, Selective, and Orally Bioavailable Fructose-1,6-Bisphosphatase Inhibitors― Design, Synthesis, In Vivo Glucose Lowering Effects, and X-ray Crystal Complex Analysis, Journal of Medicinal Chemistry, 2020,10307-10329
3.Cui Guonan#, Lai Fangfang#, Wang Xiaoyu, Chen Xiaoguang*, Xu Bailing* Design, synthesis and biological evaluation of indole-2-carboxylic acid derivatives as IDO1/TDO dual inhibitors, European Journal of Medicinal Chemistry, 2020,188: 111985
4.Zhou jie#, Ji Ming#, Yao Haiping, Cao Ran, Zhao Hailong, Wang Xiaoyu, Chen Xiaoguang*, Xu Bailing* Discovery of quinazoline-2,4(1H,3H)-dione derivatives as novel PARP1/2 inhibitors: design,synthesis and their antitumor activity, Organic & Biomolecilar Chemistry, 2018, 16(17):3189-3202
5.Cui Guonan#, Jin Jing#, Chen Hualong, Cao Ran, Chen Xiaoguang*, Xu Bailing* Synthesis and biological evaluation of pyrimidine derivatives as novel Pin1 inhibitors, Bioorganic & Medicinal Chemistry, 2018, 26(8): 2186-2197.
6.Zhou jie#, Ji Ming#, Zhu Zhixiang, Cao Ran, Chen Xiaoguang*, Xu Bailing* Discovery of 2-substituted 1H-benzo[d]imidazole-4-carboxamide derivatives as novel poly(ADP-ribose)polymerase-1 inhibitors with in vivo anti-tumor activity, European Journal of Medicinal Chemistry, 2017,132: 26-41.
7. Hailong Zhao#, Ming Ji#, Guonan Cui, Jie zhou, Fangfang Lai, Xiaoguang Chen*, Bailing Xu* Discovery of novel quinazoline-2,4(1H,3H)-dione derivatives as potent PARP-2 selective inhibitors, Bioorgnic Medicinal Chemistry 2017, 25(15): 4045-4054.
8.Hailong Zhao#, Guonan Cui#, Jing Jin, Xiaoguang Chen*, Bailing Xu*, Synthesis and Pin1 inhibitory activity of thiazole derivatives, Bioorgnic Medicinal Chemistry 2016, 24, 5911-5920.
9.Haiping Yao#, Ming Ji# , Zhixiang Zhu, Jie zhou, Ran Cao, Xiaoguang Chen*, Bailing Xu* Discovery of 1-substituted benzyl-quinazoline-2,4(1H,3H)-dione derivatives as novel poly(ADP-ribose)polymerase-1 inhibitors, Bioorgnic Medicinal Chemistry 2015, 23, 681-693.
10.Jianbo Bie#, Shuainan Liu# , Zhanmei Li, Yongzhao Mu, Bailing Xu* , Zhufang Shen*, Discovery of novel indole derivatives as allosteric inhibitors of fructose-1, 6-bisphosphatase, European Journal of Medicinal Chemistry, 2015, 90, 394-405.
11.Jianbo Bie, Shuainan Liu, Jie Zhou, Bailing Xu*, Zhufang Shen*, Design, synthesis and biological evaluation of 7-nitro-1H-indole-2-carboxylic acid derivatives as allosteric inhibitors of fructose-1,6-bisphosphatase, Bioorgnic Medicinal Chemistry 2014, 22, 1850-1862.
12.Jie Zhou,# Mingyu Ba#, Bo Wang, Haibo Zhou, Jianbo Bie, Decai Fu, Yingli Cao, Bailing Xu*, Ying Guo*, Synthesis and biological evaluation of novel quinoxalinone-based HIV-1 reverse transcriptase inhibitors, Med. Chem. Commun., 2014, 5, 441-444
13.Jie Zhou#, Jing Jin# , Yi Zhang, Yuwen, Yin, Xiaoguang Chen*, Bailing Xu*, Synthesis and antiproliferative evaluation of novel benzoimidazole-contained oxazole-bridged analogs of combretastatin A-4, European Journal of Medicinal Chemistry, 2013, 68, 222-232.
14.Chang Liu#, Jing Jin#, Liang Chen, Jie Zhou, Xiaoguang Chen*, Decai, Fu, Hongrui Song, Bailing Xu*. Synthesis and biological evaluation of novel human Pin1 inhibitors with benzophenone skeleton. Bioorg. Med. Chem. 2012, 20, 2992-2999.
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