吴德燕 男 博士 研究员 博士生导师
邮箱:wudeyan@hainanu.edu.cn
办公地址:伟德bv1946官网生物楼副楼F603室
2014年6月博士毕业于华东理工大学伟德bv1946官网,同年进入上海睿智化学研究有限公司从事药学研究工作一年,2015年7月加入中山大学伟德bv1946官网,从事药物化学相关研究;于2021年4月通过高层次人才引进到伟德bv1946官网工作至今。
1.教育背景
2009.09 - 2014.06:华东理工大学,伟德bv1946官网,博士(硕博连读)
2005.09 - 2009.06:湖南城市学院,化学与环境工程学院,本科(湖南省优秀毕业生)
2.教学情况
主讲药物分子设计与合成,制药设备与车间设计
3.科研情况
近年来与罗海彬教授通力合作,共同构建了基于靶标“磷酸二酯酶(PDEs)”的药物发现平台,目前研究方向聚焦于“基于靶标PDEs的全新药物设计、结构与成药性优化及作用机制研究”。已在国内外重要学术刊物J. Med. Chem., Acta Pharm. Sin. B, PNAS, Org. Lett., Chem. Commun.等发表论文30余篇;发明专利10项;主持国家自然科学基金面上项目、国家自然科学基金青年基金、广州市科技计划、广东省自然科学基金等项目8项。目前已有多个项目分别针对肺动脉高压、肺纤维化、衰老、肿瘤转移、肿瘤多药耐药(MDR)等疾病的研究取得重大进展,其中主持一项针对肺动脉高压治疗的1.1类创新化学药已进入临床前研究。
4.研究领域
药物分子设计、结构优化及作用机制研究;
活性天然产物全合成、结构修饰及成药性研究;
基于骨架跃迁(Scaffold Hopping)的药用优势骨架合成及成药性研究
5.科研项目
1)国家自然科学基金面上项目,吡咯色原酮类PDE5特异性抑制剂的设计、抗肺动脉高压活性及作用机制研究,2019.01-2022.12,55万,主持
2)广州市科技计划—民生科技攻关项目,抗肺动脉高压I类创新化学药(PDE5抑制剂罗达那非)的临床前研究,2018.04-2021.03,200万,主持
3)国家自然科学基金青年基金项目,抗慢性阻塞性肺病PDE4高选择性抑制剂的发现:天然产物桑辛素M的结构优化及生物活性研究,2017.01-2019.12,17.3万,主持
4)海南省自然科学基金高层次人才项目,磷酸二酯酶四型(PDE4)选择性抑制剂的合理设计与结构优化,2022.01.01-2024.12.31,10万,主持
5)BV伟德国际1946科研启动经费,基于靶标磷酸二酯酶的药物分子设计、成药性优化及抗肺动脉高压作用研究,2021.04.19-2026.04.19,150万,主持
6)广东省自然科学基金博士启动项目,老药新用导向的抗菌活性化合物发现及结构优化,2016.06-2019.06,10万,主持
7)广东省医学科研基金项目,天然产物Moracin M导向的PDE4抑制剂的设计、合成及活性研究,2016.07-2018.06,1万元,主持
8)中山大学青年教师培育基金项目,抗肺动脉高压PDE5高选择性抑制剂的设计、合成及生物活性研究,2017.01-2019.12,15万元,主持
6. 代表性论文
1)Deyan Wu#, Xuehua Zheng#, Runduo Liu, Zhe Li, Zan Jiang, Qian Zhou, Yue Huang, Xu-Nian Wu, Chen Zhang, Yi-You Huang*, Hai-Bin Luo*. Free Energy Perturbation (FEP)-Guided Scaffold Hopping. Acta Pharm. Sin. B 2022, 12, 1351-1362. (IF: 11.614)
(2)Yi-You Huang#, Yan-Fa Yu#, Chen Zhang#, Yiping Chen, Qian Zhou, Zhuoming Li, Sihang Zhou, Zhe Li, Lei Guo, Deyan Wu*, Yinuo Wu*, Hai-Bin Luo*. Validation of Phosphodiesterase-10 as a Novel Target for Pulmonary Arterial Hypertension via Highly Selective and Subnanomolar Inhibitors. J. Med. Chem. 2019, 62, 3707-3721. (IF: 7.446)
(3)Deyan Wu#, Yadan Huang#, Yiping Chen#, Yi-You Huang, Haiju Geng, Tianhua Zhang, Chen Zhang, Zhe Li, Lei Guo, Jianwen Chen, and Hai-Bin Luo*. Optimization of Chromeno[2,3-c]pyrrol-9(2H)-ones as Highly Potent, Selective, and Orally Bioavailable PDE5 Inhibitors: Structure–Activity Relationship, X-ray Crystal Structure, and Pharmacodynamic Effect on Pulmonary Arterial Hypertension. J. Med. Chem. 2018, 61, 8468-8473. (IF: 7.446) 封面论文
(4)Deyan Wu#, Tianhua Zhang#, Yiping Chen, Yadan Huang, Haiju Geng, Yanfa Yu, Chen Zhang, Zengwei Lai, Yinuo Wu, Xiaolei Guo, Jianwen Chen,* Hai-Bin Luo*. Discovery and Optimization of Chromeno[2,3-c]pyrrol-9(2H)-ones as Novel Selective and Orally Bioavailable Phosphodiesterase 5 Inhibitors for the Treatment of Pulmonary Arterial Hypertension.. J. Med. Chem. 2017, 60, 6622-6637. (IF: 7.446) 封面论文
(5)Yan-Fa Yu#, Chen Zhang#, Yi-You Huang#, Sirui Zhang, Qian Zhou, Xiangmin Li, Zengwei Lai, Zhe Li, Yuqi Gao, Yinuo Wu, Lei Guo*, Deyan Wu*, Hai-Bin Luo. Discovery and Optimization of Chromone Derivatives as Novel Selective Phosphodiesterase 10 Inhibitors. ACS Chem. Neurosci. 2020, 11, 1058-1071. (IF: 4.418)
(6)Jinxuan Li#, Jing-Yi Chen#, Ya-Lin Deng, Qian Zhou, Yinuo Wu*, Deyan Wu*, Hai-Bin Luo. Structure-Based Design, Synthesis, Biological Evaluation, and Molecular Docking of Novel PDE10 Inhibitors With Antioxidant Activities. Front. Chem. 2018, 6, 167. (IF: 5.221)
(7)Yinuo Wu, Zhe Li, Yi-You Huang, Deyan Wu, Hai-Bin Luo*. Novel Phosphodiesterase Inhibitors for Cognitive Improvement in Alzheimer’s Disease. J. Med. Chem. 2018, 61, 5467-5483. (IF: 7.446)
(8)Zhe Li#, Xin Li#, Yi-You Huang#, Yaoxing Wu#, Runduo Liu, Lingli Zhou, Yuxi Lin, Deyan Wu, Lei Zhang, Hao Liu, Ximing Xu, Kunqian Yu, Yuxia Zhang, Jun Cui*, Chang-Guo Zhan*, Xin Wang*, Hai-Bin Luo*. Identify potent SARS-CoV-2 main protease inhibitors via accelerated free energy perturbation-based virtual screening of existing drugs. PNAS 2020, 117, 27381-27387. (IF: 11.205)
(9)Senling Feng#, Huifang Zhou#, Deyan Wu, Dechong Zheng, Biao Qu, Ruiming Liu, Chen Zhang, Zhe Li, Ying Xie*, Hai-Bin Luo*. Nobiletin and its derivatives overcome multidrug resistance (MDR) in cancer: total synthesis and discovery of potent MDR reversal agents, Acta Pharm. Sin. B 2020, 10, 327-343. (IF: 11.413)
(10)Yiyou Huang#, Xin Liu#, Deyan Wu, Guihua Tang, Zengwei Lai, Xuehua Zheng*, Sheng Yin*, Hai-Bin Luo*. The Discovery, Complex Crystal Structure, and Recognition Mechanism of a Novel Natural PDE4 inhibitor from Selaginella Pulvinata. Biochem. Pharmacol. 2017, 130, 51-59. (IF: 5.858)
(11)Zhe Li#, Yiyou Huang#, Yinuo Wu, Jingyi Chen, Deyan Wu, Chang-Guo Zhan*, Hai-Bin Luo*. Absolute Binding Free Energy Calculation and Design of a Subnanomolar Inhibitor of Phosphodiesterase-10. J. Med. Chem. 2019, 62, 2099-2111. (IF: 7.446)
(12)Jinhao Liang#, Yi-You Huang#, Qian Zhou#, Yuqi Gao, Zhe Li, Deyan Wu, Si Yu, Lei Guo, Zhen Chen, Ling Huang, Steven H. Liang, Xixin He*, Ruibo Wu*, Hai-Bin Luo*. Discovery and Optimization of α-Mangostin Derivatives as Novel PDE4 Inhibitors for the Treatment of Vascular Dementia. J. Med. Chem. 2020, 63, 3370-3380. (IF: 7.446)
(13)Deyan Wu, Xuwen Zhang, Yong Xu, Yingfei Xue, Jian Li, Wei Wang,* Jin Zhu*. Organocatalytic Enantioselective Friedel–Crafts Reaction of 1-Naphthols with Isatins and an Unexpected Spontaneous Dehydration Process. Asian J. Org. Chem. 2014, 3, 480-486. (IF: 3.319)
(14)Lu Liu, Deyan Wu, Shu Zheng, Tengfei Li, Xiangmin Li, Sinan Wang, Jian Li, Hao Li*, Wei Wang*. Synthesis of Highly Functionalized Chiral 3,3′-Disubstituted Oxindoles via an Organocatalytic Enantioselective Michael Addition of Nitroalkanes to Indolylidenecyanoacetates. Organic Lett. 2012, 14, 134-137. (IF: 6.005)
(15)Lu Liu, Deyan Wu, Xiangmin Li, Sinan Wang, Hao Li, Jian Li*, Wei Wang*. Organocatalytic Enantioselective Conjugate Addition of Ketones to Isatylidine Malononitriles. Chem.Commun. 2012, 48, 1692-1694. (IF: 6.222)
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