主要研究方向为:
(1)中药民族药作用靶点及相关机制的研究;
(2)靶向药物的研究与开发;
(3)药物化学生物学研究。
欢迎有兴趣于药物化学、化学生物学、微生物与生化药学和中药民族药新药研究开发等研究领域的同学报考研究生,联系邮箱:binhe@gmc.edu.cn.
代表性论文:
1. Development of a mitochondrial sirtuin 4 FRET assay based on its activity for removing 3-hydroxy-3-methylglutaryl (HMG) modification. RSC Adv. 2021, 11, 2677-2681.
2. Direct C(sp3)-H acyloxylation of indolin-3-ones with carboxylic acids catalysed by KI. Green Chem. 2020, 22, 2354-2358.
3. Unexpected small molecules as novel SIRT2 suicide inhibitors. Bioorg. Med. Chem. 2020, 28(6), 115353.
4. Zinc-dependent Deacetylase (HDAC) Inhibitors with Different ZBG Groups. Curr. Top. Med. Chem. 2019, 19(3), 223-241.
5. The mimics of Nε-acyl-lysine derived from cysteine as sirtuin inhibitor. Bioorg. Med. Chem. Lett. 2018, 28(14), 2375-2378.
6. SIRT4 is the last puzzle of mitochondrial sirtuins. Bioorg. Med. Chem. 2018, 26(14):3861-3865.
7. Scutellarin inhibits Hela cell growth and glycolysis by inhibiting the activity of pyruvate kinase M2. Bioorg. Med. Chem. Lett. 2017, 27(24), 5404-5408.
8. SIRT2 reverses 4-oxononanoyl lysine modification on histones. J. Am. Chem. Soc. 2016, 138(38), 12304-12307.
9. A SIRT2-Selective Inhibitor Promotes c-Myc Oncoprotein Degradation and Exhibits Broad Anticancer Activity. Cancer Cell 2016, 29(3), 297-310.
10. A FRET-based assay for screening SIRT6 modulators. Eur. J. Med. Chem. 2015, 96, 245-249.
11. Thiomyristoyl peptides as cell-permeable Sirt6 inhibitors. Org. Biomol. Chem. 2014, 12(38), 7498-7502.
12. SIRT6 regulates TNF-a secretion through hydrolysis of long-chain fatty acyl lysine. Nature 2013, 496(7443), 110-113.
13. Thiosuccinyl Peptides as Sirt5-Specific Inhibitors. J. Am. Chem. Soc. 2012, 134(4), 1922-1925.
14. Sirt5 Is a NAD-Dependent Protein Lysine Demalonylase and Desuccinylase. Science 2011, 334(6057), 806-809.