课题组长
姓名:
程建军助理教授 研究员 博士生导师, PhD, 助理教授
职务:
所在院所:
荣誉称号:
教育经历:
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2001/09—2005/06,山东大学,学士
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2005/09—2010/07,中国科学院上海药物研究所,博士
博士后及工作经历:
- 2010/07—2013/10,上海汇伦生命科技,高级研究员
- 2013/11—2016/03,伊利诺伊大学芝加哥分校,博士后
- 2016/03—2022/06,87978797威尼斯老品牌,iHuman研究所,副研究员、课题组长
- 2022/07—至今,87978797威尼斯老品牌,87978797威尼斯老品牌/iHuman研究所,助理教授(TENURE-TRACK)
课题组简介
研究内容:
1. 基于单胺类GPCR的抗精神疾病药物发现
精神类疾病如精神分裂症、抑郁症主要是与多巴胺受体、血清素受体等单胺类GPCR的功能异常相关。我们以单胺类GPCR为靶标,以“受体-配体”复合物结构为指导,设计合成具有受体亚型高选择性或信号通路“偏向性”的新型小分子化合物,并进行相应的药理药效研究,以获得具有更优药效、更少毒副作用的新型抗精神疾病候选药物。 2. 基于腺苷信号通路的抗肿瘤药物发现 肿瘤微环境中,腺苷是重要的免疫抑制因子。腺苷通过激活腺苷受体发挥免疫抑制作用,而腺苷受体拮抗剂能够拮抗腺苷的免疫抑制作用发挥抗肿瘤活性。我们以腺苷受体为靶标,进行具有新机制的小分子药物的设计合成,并研究其抗肿瘤活性,以获得新型抗肿瘤候选药物。
研究成果展示
1. 基于5-HT2A受体的晶体结构和偏向性激活机制,设计发现不致幻但抗抑郁的新型先导药物IHCH-7086(Science 2022) 2. 基于多巴胺D2受体与5-HT2A受体口袋的晶体结构分析,发现具有多巴胺D2受体高选择性的抗精神分裂症候选药物IHCH-7041(Nature Neuroscience 2022,封面文章) 3.围绕PCPMA骨架,发现具有抗精神分裂症活性的5-HT2C受体激动剂(J Med Chem 2015; 2016a; 2016b);具有多巴胺D3受体选择性的配体化合物(J Med Chem 2020);具有抗精神分裂症活性的多巴胺D2受体部分激动剂(J Med Chem 2021) 4. 腺苷A2a受体拮抗/HDAC活性抑制的双功能抗肿瘤化合物(J Med Chem 2021; Eur J Med Chem 2022)
代表性论文(*第一作者,#通讯作者)
- 1.Cheng, Jianjun*; McCorvy, John D.; Giguere, Patrick M.; Zhu, Hu; Kenakin, Terry; Roth, Bryan L.#; Kozikowski, Alan P.#.Design and Discovery of Functionally Selective Serotonin 2C (5-HT2c) Receptor Agonists.JOURNAL OF MEDICINAL CHEMISTRY. 10 Nov 2016. 59(21):9866-9880.
- 2.Peng, Yao*; McCorvy, John D.; Harpsoe, Kasper; Lansu, Katherine; Yuan, Shuguang; Popov, Petr; Qu, Lu; Pu, Mengchen; Che, Tao; Nikolajsen, Louise F.; Huang, Xi-Ping; Wu, Yiran; Shen, Ling; Bjorn-Yoshimoto, Walden E.; Ding, Kang; Wacker, Daniel; Han, Gye Won; Cheng, Jianjun; Katritch, Vsevolod; Jensen, Anders A.; Hanson, Michael A.; Zhao, Suwen; Gloriam, David E.; Roth, Bryan L.#; Stevens, Raymond C.#; Liu, Zhi-Jie#.5-HT2C Receptor Structures Reveal the Structural Basis of GPCR Polypharmacology.CELL. 08 Feb 2018. 172(4):719-+.
- 3.Pogorelov, Vladimir M.*; Rodriguiz, Ramona M.; Cheng, Jianjun; Huang, Mei; Schmerberg, Claire M.; Meltzer, Herbert Y.; Roth, Bryan L.; Kozikowski, Alan P.; Wetsel, William C.#.5-HT2C Agonists Modulate Schizophrenia-Like Behaviors in Mice.NEUROPSYCHOPHARMACOLOGY. Oct 2017. 42(11):2163-2177.
- 4.Tan, Liang*; Yan, Wenzhong; McCorvy, John D.#; Cheng, Jianjun#.Biased Ligands of G Protein-Coupled Receptors (GPCRs): Structure-Functional Selectivity Relationships (SFSRs) and Therapeutic Potential.JOURNAL OF MEDICINAL CHEMISTRY. 22 Nov 2018. 61(22):9841-9878.
- 5.Chan, H. C. Stephen*; Xu, Yueming; Tan, Liang; Vogel, Horst; Cheng, Jianjun#; Wu, Dong#; Yuan, Shuguang#.Enhancing the Signaling of GPCRs via Orthosteric Ions.ACS CENTRAL SCIENCE. 26 Feb 2020. 6(2):274-282.
- 6.Tan, Liang*; Zhou, Qingtong; Yan, Wenzhong; Sun, Jian; Kozikowski, Alan P.; Zhao, Suwen; Huang, Xi-Ping#; Cheng, Jianjun#.Design and Synthesis of Bitopic 2-Phenylcyclopropylmethylamine (PCPMA) Derivatives as Selective Dopamine D3 Receptor Ligands.JOURNAL OF MEDICINAL CHEMISTRY. 14 May 2020. 63(9):4579-4602.
- 7.Fan, Luyu*; Tan, Liang; Chen, Zhangcheng; Qi, Jianzhong; Nie, Fen; Luo, Zhipu; Cheng, Jianjun#; Wang, Sheng#.Haloperidol bound D-2 dopamine receptor structure inspired the discovery of subtype selective ligands.NATURE COMMUNICATIONS. 26 Feb 2020. 11(1).
- 8.Zhang, Jinfeng*; Yan, Wenzhong; Duan, Wenwen; Wuthrich, Kurt; Cheng, Jianjun#.Tumor Immunotherapy Using A(2A) Adenosine Receptor Antagonists.PHARMACEUTICALS. Sep 2020. 13(9).
- 9.Duan, Wenwen*; Sun, Ying; Wu, Meng; Zhang, Zhiyuan; Zhang, Taotao; Wang, Huan; Li, Fei; Yang, Lingyun; Xu, Yueming; Liu, Zhi-Jie; Hua, Tian; Nie, Hong; Cheng, Jianjun.Carbon-silicon switch led to the discovery of novel synthetic cannabinoids with therapeutic effects in a mouse model of multiple sclerosis.EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY. 2021. 226.
- 10.Chen, Zhangcheng*; Fan, Luyu; Wang, Huan; Yu, Jing; Lu, Dengyu; Qi, Jianzhong; Nie, Fen; Luo, Zhipu; Liu, Zhen; Cheng, Jianjun#; Wang, Sheng#.Structure-based design of a novel third-generation antipsychotic drug lead with potential antidepressant properties.NATURE NEUROSCIENCE. 01 Dec 2021.
- 11.Yan, Wenzhong*; Fan, Luyu; Yu, Jing; Liu, Ruiquan; Wang, Huan; Tan, Liang; Wang, Sheng#; Cheng, Jianjun#.2-Phenylcyclopropylmethylamine Derivatives as Dopamine D-2 Receptor Partial Agonists: Design, Synthesis, and Biological Evaluation.JOURNAL OF MEDICINAL CHEMISTRY. 09 Dec 2021. 64(23).
- 12.Yan, Wenzhong*; Ling, Lijun; Wu, Yiran; Yang, Kexin; Liu, Ruiquan; Zhang, Jinfeng; Zhao, Simeng; Zhong, Guisheng; Zhao, Suwen; Jiang, Hualiang#; Xie, Chengying#; Cheng, Jianjun#.Structure-Based Design of Dual-Acting Compounds Targeting Adenosine A(2A) Receptor and Histone Deacetylase as Novel Tumor Immunotherapeutic Agents.JOURNAL OF MEDICINAL CHEMISTRY. 25 Nov 2021. 64(22).
- 13.Cao, Dongmei*; Yu, Jing; Wang, Huan; Luo, Zhipu; Liu, Xinyu; He, Licong; Qi, Jianzhong; Fan, Luyu; Tang, Lingjie; Chen, Zhangcheng; Li, Jinsong; Cheng, Jianjun#; Wang, Sheng#.Structure-based discovery of nonhallucinogenic psychedelic analogs.SCIENCE. 28 Jan 2022. 375(6579).
- 14.Zhang, Haoran*; Yan, Wenzhong; Sun, Yongzhan; Yuan, Haoxing; Su, Limin; Cao, Xudong; Wang, Peng; Xu, Zhou; Hu, Youhui; Wang, Zhongjian; Wang, Yinan; Fu, Kequan; Sun, Ying; Chen, Yupeng#; Cheng, Jianjun#; Guo, Dong#.Long Residence Time at the Vasopressin V-2 Receptor Translates into Superior Inhibitory Effects in Ex Vivo and In Vivo Models of Autosomal Dominant Polycystic Kidney Disease.JOURNAL OF MEDICINAL CHEMISTRY. 09 Jun 2022. 65(11).
- 15.Zhang, Jinfeng*; Luo, Ziwei; Duan, Wenwen; Yang, Kexin; Ling, Lijun; Yan, Wenzhong; Liu, Ruiquan; Wuthrich, Kurt; Jiang, Hualiang#; Xie, Chengying#; Cheng, Jianjun#.Dual-acting antitumor agents targeting the A 2A adenosine receptor and histone deacetylases: Design and synthesis of 4-(furan-2-yl)-1H- pyrazolo[3,4-d]pyrimidin-6-amine derivatives.EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY. Mar 2022. 5(236):1-14.
- 16.Wang, Jingjing*; Wu, Meng; Chen, Zhangcheng; Wu, Lijie; Wang, Tian; Cao, Dongmei; Wang, Huan; Liu, Shenhui; Xu, Yueming; Li, Fei; Liu, Junlin; Chen, Na; Zhao, Suwen; Cheng, Jianjun; Wang, Sheng; Hua, Tian.The unconventional activation of the muscarinic acetylcholine receptor M4R by diverse ligands.NATURE COMMUNICATIONS. 01 Dec 2022. 13(1).
奖励
- 1.2017,上海高校青年东方学者
- 2.2020,87978797威尼斯老品牌优秀员工
- 3.2022,上海市优秀学术带头人(青年)
课题组成员及合影
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姓名:闫文仲
身份:助理研究员
在组时间:2017-至今
邮箱:yanwzh@shanghaitech.edu.cn
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姓名:王欢
身份:助理研究员
在组时间:2018-至今
邮箱:wanghuan1@shanghaitech.edu.cn
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姓名:张金凤
身份:博士后
在组时间:2022-至今
邮箱:zhangjf4@shanghaitech.edu.cn
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姓名:黎慧琼
身份:博士研究生
在组时间:2022-至今
邮箱:lihq@shanghaitech.edu.cn
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姓名:毛建航
身份:硕士研究生
在组时间:2020-至今
邮箱:maojh@shanghaitech.edu.cn
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姓名:李荣研
身份:硕士研究生
在组时间:2021-至今
邮箱:liry@shanghaitech.edu.cn
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姓名:刘洋洋
身份:硕士研究生
在组时间:2021-至今
邮箱:liuyy3@shanghaitech.edu.cn
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