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周洁,博士,副研究员,硕士生导师,
2005进入中国医学科学院药物研究所工作至今,先后任助理研究员、副研究员,主要从事创新药物研发、有机合成等方面的工作。近年来,主持或参与科研项目共10项,其中主持国家自然青年基金项目1项,药物所基本科研业务费3项,参与的项目包括国家科技重大专项2项,中国医学科学院医学与健康科技创新工程1项,国自然面上项目3项等。近年来发表SCI论文10余篇。申请发明专利6项,授权2项。
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支持扩展名:.rar .zip .doc .docx .pdf .jpg .png .jpeg抗肿瘤药物分子的设计、合成及活性研究
抗糖尿病药物分子的设计、合成及活性研究
靶向钾离子通道阻断剂的设计、合成及生物功能研究
发表论文:
1. Jie Zhou, Jianbo Bie, Xiaoyu Wang, Quan Liu, Rongrui Li, Hualong Chen, Jinping Hu, Hui Cao, Wenming Ji, Yan Li, Shuainan Liu, Zhufang Shen, Bailing Xu,Discovery of N‑Arylsulfonyl-Indole-2-CarboxamideDerivatives as Potent, Selective, and Orally BioavailableFructose-1,6-Bisphosphatase Inhibitors Design, Synthesis, In Vivo GlucoseLowering Effects, and X‑ray Crystal Complex Analysis . J. Med. Chem. 2020, 63, 10307-10329
2. Jie Zhou, Ming Ji, Haiping Yao, Ran Cao, Hailong Zhao, Xiaoyu Wang,Xiaoguang Chen, Bailing Xu. Discovery of quinazoline-2,4(1H,3H)-dione derivatives asnovel PARP-1/2 inhibitors: design, synthesis and their antitumor activity, Organic& Biomolecular Chemistry, 2018, 16, 3189-3220
3. JieZhou, Ming Ji, Zhixiang Zhu, Ran Cao, Xiaoguang Chen, Bailing Xu,Discovery of 2-substituted 1H-benzo[d]immidazole-4-carboxamide derivatives asnovel poly(ADP-ribose) polymerase-1 inhibitors with in vivo anti-tumor activity, EuropeanJournal of Medicinal Chemistry, 2017, 132, 26-41.
4. 周洁,朱枝祥,季鸣,曹冉,陈晓光,徐柏玲,3-氨基苯甲酰胺衍生物PARP-1抑制剂的设计、合成及活性评价,中国药物化学杂志,2016, 26, 165-174.
5. JieZhou, Mingyu Ba, Bo Wang, Haibo Zhou, Jianbo Bie, Decai Fu, Yingli Cao,Bailing Xu, Ying Guo. Synthesis and biological evaluation of novelquinoxalinone-based HIV-1 reverse transcriptase inhibitors. MedChemComm,2014, 5, 441-444.
6. JieZhou, Jing Jin, Yi Zhang, Yuwen, Yin, Xiaoguang Chen, Bailing Xu.Synthesis and antiproliferative evaluation of novel benzoimidazole-containedoxazole-bridged analogs of combretastatin A-4. European Journal of Medicinal Chemistry,2013, 68, 222-232.
7. 周 洁, 朱枝祥, 陈晓光, 徐柏玲. 氮杂吲哚类PARP-1抑制剂的合成及活性评价,药学学报,2013, 48, 1792-1799.
8. JieZhou, Yi Zhang, Yiwen Cui, Zhanmei Li, Hongrui Song, Jinhua Dong,Xiaoguang Chen, Bailing Xu. Synthesis and cytotoxic evaluation of N-(4-methoxy-1H benzo[d]imidazol-7-yl)-arylsulfonamide and N-aryl-(4-methoxy-1H-benzo[d] imidazol)- 7-sulfonamide analogs of combretastatin A-4. Journal of AsianNatural Products Research,2011, 3, 330-340.
9. Hailong Zhao, Ming Ji, Guonan Cui, Jie Zhou, Fangfang Lai, XiaoguangChen, Bailing Xu, Discovery of novel quinazoline-2,4(1H,3H)-dione derivativesas potent PARP-2 selective inhibitors, Bioorganic & Medicinal Chemistry. 2017,25 , 4045-4054.
10. QinZhou, Ming Ji, Jie zhou, JingJin, Nina Xue, Ju Chen, Bailing xu, Xiaoguang chen , Poly (ADP-ribose) polymerases inhibitor, Zj6413, as apotential therapeuticagent against breast cancer, Biochemical Pharmacology,2016, 107, 29-40.
11. Hai-Long Zhao, Hua-Long Chen, Jie zhou, Bailing xu, Structureidentification of 4-amino -2-(arylamino)thiazole-5-carboxylic esters, Chinese ChemicalLetters, 2016, 27,302-304.
12. Haiping Yao, Ming Ji, Zhixiang Zhu, Jie Zhou, Ran Cao, Xiaoguang Chen,Bailing Xu. Discovery of 1-substituted benzyl-quinazoline-2,4(1H,3H)-dionederivatives as novel poly (ADP-ribose) polymerase-1 inhibitors. Bioorganic &Medicinal Chemistry. 2015,23, 681–693.
授权专利
1. 徐柏玲、陈晓光、周洁、季鸣、姚海平、周秦;含有哌嗪酮的喹唑啉酮类PARP-1/2抑制剂及其制备方法、药物组合物和用途;专利号:ZL201610108263.3, 专利授权日:2020-5-7.
2. 徐柏玲、申竹芳、别建波、穆永钊、刘率男、周洁、李彩娜、曹冉、环弈、孙淑娟, N-酰基磺酰胺类FBPase抑制剂、其制备方法、药物组合物及用途; 专利号:ZL 2016 10105864.9, 专利授权日:2020-10-9.
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