基本信息
年寅 男 硕导 中国科学院昆明植物研究所
电子邮件: nianyin@mail.kib.ac.cn
通信地址: 云南省昆明市盘龙区蓝黑路132号,华立楼B406
邮政编码:
电子邮件: nianyin@mail.kib.ac.cn
通信地址: 云南省昆明市盘龙区蓝黑路132号,华立楼B406
邮政编码:
研究领域
膜蛋白(离子通道)的结构功能及其天然药物研究
招生信息
招生专业
100706-药理学100701-药物化学071010-生物化学与分子生物学
招生方向
离子通道天然活性分子的发现、机理及成药性研究离子通道结构功能研究
教育背景
2009-05--2010-04 美国伊利诺伊斯大学芝加哥分校 访问学生2005-09--2011-01 中国科学院昆明植物研究所 博士学位2001-09--2005-07 广东中山大学 学士学位
工作经历
工作简历
2024-02~现在, 中国科学院昆明植物研究所, 研究员(专题组组长)2020-07~2024-02,中国科学院昆明植物研究所, 副研究员(专题组组长)2019-01~2020-06,中国科学院昆明动物研究所, 副研究员2016-03~2017-03,美国贝勒医学院, 博士后2013-11~2018-12,中国科学院昆明动物研究所, 助理研究员2011-05~2013-10,云南生物谷灯盏花花药业有限公司和中国科学院昆明植物研究所, 企业联合培养博士后
社会兼职
2023-12-01-2028-11-30,沈阳药科大学硕士研究生联合培养导师, 硕士生导师
2021-12-31-今,SCI期刊Natural Products and Bioprospecting青年编委, 论文审稿
2021-12-31-今,SCI期刊Natural Products and Bioprospecting青年编委, 论文审稿
专利与奖励
专利成果
( 1 ) 环维黄杨星D在制药中的应用, 发明专利, 2023, 第 1 作者, 专利号: CN 111170967 A( 2 ) 黄杨生物碱Buxusemine H和Buxusemine L 在制药中的应用, 发明专利, 2024, 第 1 作者, 专利号: CN 117338790 A( 3 ) 酰基间苯三酚类衍生物及其药物组合物和应用, 发明专利, 2020, 第 2 作者, 专利号: CN111170967A( 4 ) 去芳化异戊烯基酰基间苯三酚类衍生物及其药物组合物和应用, 发明专利, 2020, 第 2 作者, 专利号: CN111056935A( 5 ) 一种升麻及其提取物的新用途, 发明专利, 2018, 第 4 作者, 专利号: CN108186656A( 6 ) 石松生物碱lycoplanineA及其药物组合物与其制备方法和应用, 专利授权, 2017, 第 4 作者, 专利号: CN107365316A( 7 ) 蜘蛛香环烯醚萜部位在制备N-型钙通道抑制剂中的应用, 发明专利, 2015, 第 3 作者, 专利号: CN104721180A( 8 ) 环阿尔廷型三萜化合物及其应用, 发明专利, 2013, 第 4 作者, 专利号: CN103145795A( 9 ) 一种色酮化合物的医药用途, 发明专利, 2013, 第 4 作者, 专利号: CN103156838A( 10 ) 一种升麻三萜类化合物及其应用, 发明专利, 2013, 第 4 作者, 专利号: CN103145794A( 11 ) 羊毛甾烷三萜类化合物及其应用, 发明专利, 2013, 第 4 作者, 专利号: CN103159821A( 12 ) 化合物(20R,24R)-24,25-16,23-23,27-三环氧-12-乙酰氧基-9,19-环羊毛甾烷-3-O-β-D-吡喃木糖甙在制药中的应用, 发明专利, 2012, 第 3 作者, 专利号: CN102614208A( 13 ) 3,4-裂-4-羟基-3-升麻酸甲酯,含其的药物组合物及其制备方法和应用, 发明专利, 2012, 第 2 作者, 专利号: CN102391279A( 14 ) 阿尔廷烷型三萜化合物及其药物组合物和其制备方法与应用, 发明专利, 2009, 第 2 作者, 专利号: CN101570563A
出版信息
发表论文
[1] Gong Ye, Liu Rui, Zha Hongjing, Dong Ding, Lu Nihong, Yan Hui, Wan Luosheng, Nian, Yin. Analgesic Buxus alkaloids with enhanced selectivity for the low voltage-gated calcium channel Cav3.2 over Cav3.1 through a new binding mode.. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION[J]. 2024, 第 8 作者 通讯作者 63(1): e202313461, https://onlinelibrary.wiley.com/doi/10.1002/anie.202313461.[2] Zhao Jianjun, Du Shuzong, Hu Kun, Hu Yali, Xia Fan, Ye Yansong, Yang Jian, Nian Yin, Xu Gang. Abietane derived diterpenoids as Cav3.1 antagonists from Salvia digitaloides. CHINESE CHEMICAL LETTERS[J]. 2023, 第 8 作者 通讯作者 34(4): 107737, http://dx.doi.org/10.1016/j.cclet.2022.08.017.[3] Ye YanSong, Liu Rui, Jiang NaNa, Li SongYu, Nian Yin, Xu Gang. Caged polycyclic polyprenylated acylphloroglucinols as Ca(v)3.2 low voltage-gated Ca2+ channel inhibitors from Hypericum curvisepalum. CHEMICAL COMMUNICATIONS[J]. 2022, 第 5 作者 通讯作者 58(94): 13135-13138, http://dx.doi.org/10.1039/d2cc05396a.[4] Xia Fan, Du Shuzong, Wu Mingkun, Liu Rui, Ye Yansong, Yang Jian, Xu Gang, Nian Yin. Icetexane diterpenoids as Cav3.2 T-type calcium channel inhibitors from Salvia prattii and analgesic effect of their Semi-synthesized derivatives. BIOORGANIC CHEMISTRY[J]. 2022, 第 8 作者 通讯作者 128: http://dx.doi.org/10.1016/j.bioorg.2022.106059.[5] Su Deyuan, Gong Ye, Li Songyu, Yang Jian, Nian Yin. Cyclovirobuxine D, a cardiovascular drug from traditional Chinese medicine, alleviates inflammatory and neuropathic pain mainly via inhibition of voltage-gated Ca(v)3.2 channels. FRONTIERS IN PHARMACOLOGY[J]. 2022, 第 5 作者 通讯作者 13: http://dx.doi.org/10.3389/fphar.2022.1081697.[6] Hu Guilin, Dong Ding, Du Shuzong, Peng Xingrong, Wu Mingkun, Shi Qiangqiang, Hu Kun, Hong Defu, Wang Xiaoyuan, Zhou Lin, Nian Yin, Qiu Minghua. Discovery of novel coffee diterpenoids with inhibitions on Ca(v)3.1 low voltage-gated Ca2+ channel. FOOD CHEMISTRY[J]. 2022, 第 11 作者 通讯作者 376: http://dx.doi.org/10.1016/j.foodchem.2021.131923.[7] Xia Fan, Du Shuzong, Wu Mingkun, Liu Rui, Ye Yansong, Yang Jian, Xu Gang, Nian Yin. Icetexane Diterpenoids as Cav3.2 T-type calcium channel inhibitors from Salvia prattii and Analgesic Effect of Their Semi-synthesized Derivatives. BIOORGANIC CHEMISTRY[J]. 2022, 第 8 作者 通讯作者 http://dx.doi.org/10.1016/j.bioorg.2022.106059.[8] Hu, GuiLin, Peng, XingRong, Dong, Ding, Nian, Yin, Gao, Ya, Wang, XiaoYuan, Hong, DeFu, Qiu, MingHua. New ent-kaurane diterpenes from the roasted arabica coffee beans and molecular docking to alpha-glucosidase. FOOD CHEMISTRY[J]. 2021, 第 4 作者345: http://dx.doi.org/10.1016/j.foodchem.2020.128823.[9] Zhan, Rui, Du, ShuZong, Duan, ZhiHang, Nian, Yin, Chen, YeGao. Scholarinine A, a N-3 type caged-monoterpene indole alkaloid as Ca(v)3.1 T-type calcium channel inhibitor from Alstonia scholaris. TETRAHEDRON LETTERS[J]. 2020, 第 4 作者 通讯作者 61(1): http://dx.doi.org/10.1016/j.tetlet.2019.151354.[10] Wang Lie, Qian Hongwu, Nian Yin, Han Yimo, Ren Zhenning, Zhang Hanzhi, Hu Liya, Prasad, B V Venkataram, Laganowsky, Arthur, Yan Nieng, Zhou Ming. Structure and mechanism of human diacylglycerol O-acyltransferase 1. NATURE[J]. 2020, 第 3 作者581(7808): 329-+, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7255049/.[11] Ye, YanSong, Li, WenYan, Du, ShuZong, Yang, Jian, Nian, Yin, Xu, Gang. Congenetic Hybrids Derived from Dearomatized Isoprenylated Acylphloroglucinol with Opposite Effects on Ca(v)3.1 Low Voltage Gated Ca2+ Channel. JOURNAL OF MEDICINAL CHEMISTRY[J]. 2020, 第 5 作者 通讯作者 63(4): 1709-1716, https://www.webofscience.com/wos/woscc/full-record/WOS:000517673100018.[12] Ye, YanSong, Du, ShuZong, Jiang, NaNa, Xu, HongXi, Yang, Jian, Fu, WenWei, Nian, Yin, Xu, Gang. Novel Meroterpenoids from Hypericum patulum: Highly Potent Late Na(v)1.5 Sodium Current Inhibitors. ORGANIC LETTERS[J]. 2020, 第 7 作者 通讯作者 22(16): 6339-6343, http://dx.doi.org/10.1021/acs.orglett.0c02170.[13] Jiang, NaNa, Du, ShuZong, Ye, YanSong, Yan, Hui, Yang, XingWei, Yang, Jian, Nian, Yin, Xu, Gang. Hyphenone A, the first 3,3-diisoprenylated bicyclic polyprenylated acylphloroglucinols as Ca(v)3.1 T-type calcium channel inhibitor from Hypericum henryi. TETRAHEDRON LETTERS[J]. 2019, 第 7 作者 通讯作者 60(45): https://www.webofscience.com/wos/woscc/full-record/WOS:000495490500006.[14] Xia, Fan, Li, WenYan, Yang, XingWei, Yang, Jian, Li, Xian, Nian, Yin, Xu, Gang. Salpratlactones A and B: A Pair of cis-trans Tautomeric Abietanes as Ca(v)3.1 T-Type Calcium Channel Agonists from Salvia prattii. ORGANIC LETTERS[J]. 2019, 第 6 作者 通讯作者 21(14): 5670-5674, https://www.webofscience.com/wos/woscc/full-record/WOS:000476957200062.[15] Nian Yin. Two Diterpenoids with Two Skeletons from Euphorbia peplus.. Organic Letters. 2018, 第 1 作者[16] Zhou, Jun, Dong, Fa-Wu, Jiang, He-Hai, Yang, Liu, Gong, Ye, Zi, Cheng-Ting, Yang, Dan, Ye, Chen-Jun, Li, Huan, Yang, Jian, Nian, Yin, Hu, Jiang-Miao. Valepotriates From the Roots and Rhizomes of Valeriana jatamansi Jones as Novel N-Type Calcium Channel Antagonists. JOURNAL OF ETHNOPHARMACOLOGY[J]. 2018, 第 11 作者222: 208-216, http://www.irgrid.ac.cn/handle/1471x/1781692.[17] Nian, Yin, Lu, NiHong, Liu, XiaoLing, Li, DaShan, Zhou, Lin, Qiu, MingHua. Antiacetylcholinesterase triterpenes from the fruits of Cimicifuga yunnanensis. RSCADVANCES[J]. 2018, 第 1 作者8(14): 7832-7838, https://www.webofscience.com/wos/woscc/full-record/WOS:000425647000058.[18] Ren, Zhenning, Lee, Jumin, Moosa, Mahdi Muhammad, Nian, Yin, Hu, Liya, Xu, Zhichun, McCoy, Jason G, Ferreon, Allan Chris M, Im, Wonpil, Zhou, Ming. Structure of an EIIC sugar transporter trapped in an inward-facing conformation. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA[J]. 2018, 第 4 作者115(23): 5962-5967, http://dx.doi.org/10.1073/pnas.1800647115.[19] 代晓丽, 刘静, 年寅, 邱明华, 张继虹. 环阿尔廷烷型四环三萜化合物对HCT116细胞增殖、细胞周期和凋亡的影响. 中国药理学通报[J]. 2018, 第 3 作者34(1): 91-96, http://lib.cqvip.com/Qikan/Article/Detail?id=674133335.[20] Dai, Xiaoli, Liu, Jing, Nian, Yin, Qiu, MingHua, Luo, Ying, Zhang, Jihong. A novel cycloartane triterpenoid from Cimicifuga induces apoptotic and autophagic cell death in human colon cancer HT-29 cells. ONCOLOGY REPORTS[J]. 2017, 第 3 作者37(4): 2079-2086, http://www.irgrid.ac.cn/handle/1471x/1185345.[21] Jiang, HeHai, Dong, Wu, Zhou, Jun, Hu, JiangMiao, Yang, Jian, Nian, Yin. Ca(v)2.2 and Ca(v)3.1 calcium channel inhibitors from Valeriana jatamansi Jones. RSC ADVANCES[J]. 2017, 第 6 作者 通讯作者 7(72): 45878-45884, https://www.webofscience.com/wos/woscc/full-record/WOS:000412147000075.[22] Nian, Yin, Yan, Hui, Li, XiaoNian, Zhou, Lin, Qiu, MingHua. Cimifrigines A-G, cytotoxic triterpenes with an oxime group from the flowers of Cimicifuga frigida. RSC ADVANCES[J]. 2017, 第 1 作者7(61): 38557-38564, http://dx.doi.org/10.1039/c7ra07275a.[23] Nian Yin. Cimifrigines A-G, Cytotoxic Triterpenes with an Oxime Group from the Flowers of Cimicifuga frigid.. RSCADVANCES. 2017, 第 1 作者[24] Yang, YeKun, Xie, Sida, Xu, Wanxuan, Nian, Yin, Liu, XiaoLing, Peng, XingRong, Ding, ZhongTao, Qiu, MingHua. Six new physalins from Physalis alkekengi var. franchetii and their cytotoxicity and antibacterial activity. FITOTERAPIA[J]. 2016, 第 4 作者112: 144-152, http://www.irgrid.ac.cn/handle/1471x/1175693.[25] Zhu, GuoLei, Nian, Yin, Zhu, DiFan, Wan, LuoSheng, Bao, NiMan, Wang, WeiHua, Zhou, Lin, Qiu, MingHua. Cytotoxic 9,19-cycloartane triterpenoids from the roots of Cimicifuga foetida L.. PHYTOCHEMISTRY LETTERS[J]. 2016, 第 2 作者18(1): 105-112, http://dx.doi.org/10.1016/j.phytol.2016.06.002.[26] Kong, Yanjie, Li, Fubin, Nian, Yin, Zhou, Zhongmei, Yang, Runxiang, Qiu, MingHua, Chen, Ceshi. KHF16 is a Leading Structure from Cimicifuga foetida that Suppresses Breast Cancer Partially by Inhibiting the NF-kappa B Signaling Pathway. THERANOSTICS[J]. 2016, 第 3 作者6(6): 875-886, http://www.irgrid.ac.cn/handle/1471x/1109578.[27] Yue, Grace GarLee, Xie, Sida, Lee, Julia KinMing, Kwok, HinFai, Gao, Si, Nian, Yin, Wu, XiaoXiao, Wong, ChunKwok, Qiu, MingHua, Lau, Clara BikSan. New potential beneficial effects of actein, a triterpene glycoside isolated from Cimicifuga species, in breast cancer treatment. SCIENTIFIC REPORTS[J]. 2016, 第 6 作者6(1): http://www.irgrid.ac.cn/handle/1471x/1140919.[28] Wang, WeiHua, Nian, Yin, He, YuJiao, Wan, LuoSheng, Bao, NiMan, Zhu, GuoLei, Wang, Fei, Qiu, Minghua. New cycloartane triterpenes from the aerial parts of Cimicifuga heracleifolia. TETRAHEDRON[J]. 2015, 第 2 作者71(42): 8018-8025, http://dx.doi.org/10.1016/j.tet.2015.08.057.[29] Nian, Yin, Yang, Jing, Liu, TongYang, Luo, Ying, Zhang, JiHong, Qiu, MingHua. New Anti-angiogenic Leading Structure Discovered in the Fruit of Cimicifuga yunnanensis. SCIENTIFIC REPORTS[J]. 2015, 第 1 作者5: http://www.irgrid.ac.cn/handle/1471x/959063.[30] Chen, JianChao, Yuan, XiaoXi, Zhou, Lin, Liu, JieQing, Nian, Yin, Li, ZhongRong, Li, Yan, Xie, MingJin, Qiu, MingHua. Four New Cucurbitacins from the Fruit of Momordica charantia. HELVETICA CHIMICA ACTA[J]. 2014, 第 5 作者97(11): 1546-1554, http://www.irgrid.ac.cn/handle/1471x/929653.[31] Bao, NiMan, Nian, Yin, Zhu, GuoLei, Wang, WeiHua, Zhou, Lin, Qiu, MingHua. Cytotoxic 9,19-cycloartane triterpenes from the aerial parts of Cimicifuga yunnanensis. FITOTERAPIA[J]. 2014, 第 2 作者99: 191-197, http://www.irgrid.ac.cn/handle/1471x/959035.[32] Zhu DiFan, Nian Yin, Wang HaiYan, Zhang ZhiRun, Song YanBo, Li RongTao, Qiu MingHua. New 9, 19-cycloartane triterpenoid from the root of Cimicifuga foetida. CHINESE JOURNAL OF NATURAL MEDICINES[J]. 2014, 第 2 作者12(4): 294-296, http://dx.doi.org/10.1016/S1875-5364(14)60057-1.[33] 王卫华, 曽晓鹰, 年寅, 杨元凤, 夏建军, 邓媛元, 李忠荣, 邱明华. 姜酮的NMR解析. 云南大学学报(自然科学版)[J]. 2013, 第 3 作者35(4): 530-535, http://www.irgrid.ac.cn/handle/1471x/832411.[34] Yin Nian, HaiYanWang, Lin Zhou, Jia Su, Yan Li, MingHua Qiu. Cytotoxic Cycloartane Triterpenes of the TraditionalChinese Medicine "Shengma" (Cimicifuga dahurica). PLANTA MED[J]. 2013, 第 1 作者79: 60–69, http://ir.kib.ac.cn/handle/151853/52984.[35] Nian, Yin, Zhu, Hui, Tang, WenRu, Luo, Yin, Du, Jiang, Qiu, MingHua. Triterpenes from the Aerial Parts of Cimicifuga yunnanensis and Their Antiproliferative Effects on p53(N236S) Mouse Embryonic Fibroblasts. JOURNAL OF NATURAL PRODUCTS[J]. 2013, 第 1 作者76(5): 896-902, http://www.irgrid.ac.cn/handle/1471x/660284.[36] Lu, Lu, Chen, JianChao, Li, Yan, Qing, Chen, Wang, YuanYuan, Nian, Yin, Qiu, MingHua. Studies on the Constituents of Cimicifuga foetida Collected in Guizhou Province and Their Cytotoxic Activities. CHEMICAL & PHARMACEUTICAL BULLETIN[J]. 2012, 第 6 作者60(5): 571-577, http://dx.doi.org/10.1248/cpb.60.571.[37] Nian, Yin, Wang, HaiYan, Su, Jia, Zhou, Lin, Qiu, MingHua. A cytotoxic 4 alpha-methyl steroid from the aerial parts of Cimicifuga foetida L. FITOTERAPIA[J]. 2012, 第 1 作者83(2): 293-297, http://www.irgrid.ac.cn/handle/1471x/448456.[38] Wang Haiyan, Nian Yin, Ma Chengyou, Liu Jieqing, Song Yanho, Zhou Lin, Qiu Minghua. Four New 9,19-Cyclolanostane Triterpenes from the Rhizomes of Cimicifuga foetida Collected in Yulong. CHINESE JOURNAL OF CHEMISTRY[J]. 2012, 第 2 作者30(6): 1265-1268, http://lib.cqvip.com/Qikan/Article/Detail?id=42601398.[39] Fang, ZhongZe, Nian, Yin, Li, Wei, Wu, JingJing, Ge, GuangBo, Dong, PeiPei, Zhang, YanYan, Qiu, MingHua, Liu, Lei, Yang, Ling. Cycloartane Triterpenoids from Cimicifuga yunnanensis induce Apoptosis of Breast Cancer Cells (MCF7) via p53-dependent Mitochondrial Signaling Pathway. PHYTOTHERAPY RESEARCH[J]. 2011, 第 2 作者25(1): 17-24, http://dx.doi.org/10.1002/ptr.3222.[40] Li, DaShan, Nian, Yin, Sun, Yun, Qiu, MingHua. Three New Cycloartane (= 9,19-Cyclolanostane) Glycosides from Cimicifuga foetida. HELVETICA CHIMICA ACTA[J]. 2011, 第 2 作者94(4): 632-638, http://www.irgrid.ac.cn/handle/1471x/392907.[41] Lu, Lu, Chen, JianChao, Song, HeJiao, Li, Yan, Nian, Yin, Qui, MingHua. Five New Triterpene Bisglycosides with Acyclic Side Chains from the Rhizomes of Cimicifuga foetida L.. CHEMICAL & PHARMACEUTICAL BULLETIN[J]. 2010, 第 5 作者58(5): 729-733, https://www.webofscience.com/wos/woscc/full-record/WOS:000277019100024.[42] Lu, Lu, Chen, Jianchao, Nian, Yin, Sun, Yun, Qiu, Minghua. Trinor-cycloartane Glycosides from the Rhizomes of Cimicifuga foetida. MOLECULES[J]. 2009, 第 3 作者14(4): 1578-1584, https://doaj.org/article/cfd0407cbeed4415a150ab5658f4dd6f.[43] Sun, Lirong, Yan, Jian, Nian, Yin, Zhou, Lin, Zhang, Hongjie, Qiu, Minghua. New triterpene diglycosides from the rhizome of Cimifuga foetida. MOLECULES[J]. 2008, 第 3 作者13(8): 1712-1721, https://doaj.org/article/0340c46d86b245f39358871e75e1337e.[44] Yin Nian, HaiYan Wang, Lin Zhou, Jia Su, Yan Li, MingHua Qiu. Cytotoxic Cycloartane Triterpenes of Traditional Chinese Medicine "Shengma" (Cimicifugadahurica). PLANTA MED[J]. 第 1 作者1-51, http://ir.kib.ac.cn/handle/151853/53141.
科研活动
科研项目
( 1 ) 金丝桃属植物中特色间苯三酚类T-型钙通道活性成分的研究, 负责人, 国家任务, 2021-01--2024-12( 2 ) 第二次青藏高原综合科学考察研究,“藏药资源的挖掘利用”专题子课题“藏药中特色化学成分的活性研究”, 负责人, 国家任务, 2019-01--2024-12( 3 ) 中国科学院西部之光“西部青年学者”项目, 负责人, 中国科学院计划, 2021-01--2023-12( 4 ) 云南省杰出青年研究专项, 负责人, 地方任务, 2021-01--2023-12( 5 ) 云南省青年拔尖人才专项经费, 负责人, 地方任务, 2021-01--2025-12( 6 ) 灵芝杂萜GMs15抗典型失神癫痫机理研究, 负责人, 地方任务, 2020-09--2023-08( 7 ) 优秀人才启动经费, 负责人, 研究所自主部署, 2020-07--2025-06( 8 ) 重要天然产物化学成分及生物活性研究, 负责人, 境内委托项目, 2022-03--2025-02( 9 ) 云南高山植物鸡桑和草珊瑚中美白等功效成分的研究, 负责人, 境内委托项目, 2023-04--2025-12( 10 ) 离子通道天然活性分子筛选、机制及成药性研究, 负责人, 地方任务, 2024-05--2025-12( 11 ) PPAP类天然分子的离子通道活性筛选及作用机制研究, 负责人, 中国科学院计划, 2021-01--2023-12( 12 ) NYZY01和TTX缓解疼痛作用研究, 负责人, 境内委托项目, 2022-01--2022-12( 13 ) 高原动物肠道共生菌次生代谢产物研究, 负责人, 境内委托项目, 2020-10--2022-12
参与会议
(1)黄杨生物碱靶向Cav3.2的新型拮抗机理研究 第十七届全国生化与分子药理学学术会议 2023-10-27(2)Buxus alkaloids targeting Cav3.2 via a new antagonistic mechanism 第十四届全国天然有机化学学术会议 年寅 2023-09-23(3)Discovery of Novel Natural Small Molecules Targeting Ion Channels 第十四届生物毒素毒理学术大会 2019-08-16(4)作用于离子通道天然活性分子的挖掘 第一届中国科学院药物创新研究院“百草”论坛 2019-07-26(5)Discovery of novel natural small molecules targeting ion channels 2018精准医疗暨离子通道国际论坛 2018-11-14
指导学生
现指导学生
李松谕 硕士研究生 105500-药学
伍铭坤 硕士研究生 105500-药学
马梦蝶 硕士研究生 105500-药学