社会兼职情况:军事医学科学院卫生学环境医学研究所科学技术委员会委员,中国医药生物技术协会单克隆抗体专业委员会委员,国家自然基金、北京市和天津市自然基金函审评委,863计划评审专家库成员;中国药理与毒理学杂志、中国药理学通报、国际药学研究杂志、生命的化学和中国应用生理学等多个杂志评审专家,PLoS ONE、Current Analytical Chemistry、Mini-reviews in Medicinal Chemistry杂志审稿人,福建医科大学药学院客座教授。
研究方向:
(1)抗肿瘤药物的新药设计与活性评价;
(2)肿瘤耐药分子网络机制及克服新策略;
(3)环境与肿瘤药学;
(4)极端特殊环境因素(高原、寒区、热区)损伤的防治;
近五年发表SCI论文(按时间排序)
1. Gu X, Tang X, Zhao Q, Peng H*(通讯作者), Peng S, Zhang Y*. Discovery of alkoxyl biphenyl derivatives bearing dibenzo[c,e]azepine scaffold as potential dual inhibitors of P-glycoprotein and breast cancer resistance protein. Bioorg Med Chem Lett. 2014; 24(15): 3419-21 IF: 2.331
2. Huang W#, Dong Z#, Wang F#, Peng H, Liu JY, Zhang JT. A Small Molecule Compound Targeting STAT3 DNA-Binding Domain Inhibits Cancer Cell Proliferation, Migration, and Invasion. ACS Chem Biol. 2014 May 16; 9(5):1188-96 IF: 5.356
3. Xi Y, Wu X, Gao L, Shao Y, Peng H, Chen H, Chen H, Hu X, Yue J. Improving the Anti-Toxin Abilities of the CMG2-Fc Fusion Protein with the Aid of Computational Design. PLoS One. 2014 Aug 7;9(8):e104674 IF: 3.534
4. Jia Y; Zhang Y, Qiao C, Liu G, Zhao Q, Zhou T, Chen G, Li Y, Feng J, Li Y; Zhang Q*, Peng H*(通讯作者); IGF-1R and ErbB3/HER3 Contribute to Enhanced Proliferation and Carcinogenesis in Trastuzumab-resistant Ovarian Cancer model. Biochem Bioph Res Comm 2013; 436(4):740-745. IF: 2.281
5. Zhang SL, Wei YX, Li Q, Sun HP, Peng H*(通讯作者), You QD*; Pharmacophore-based drug design and biological evaluation of novel ABCB1 inhibitors. Chem Biol Drug Des. 2013; 81(3):349-358. IF: 2.507
6. Li Z, Peng H, Qin L, Qi J, Zuo X, Liu JY, Zhang JT; Determinants of
7. Dong Z, Qi J, Peng H, Liu J, Zhang JT; Spectrin domain of eukaryotic initiation factor
8. Wang Q, Feng J, Wang J, Zhang X, Zhang D, Zhu T, Wang W, Wang X, Jin J,
9. Wei Y, Ma Y, Zhao Q, Ren Z, Li Y, Hou T*, Peng H*(通讯作者); New use for an old drug: inhibiting ABCG2 with sorafenib. Mol Cancer Ther. 2012; 11(8):1693-1702 IF: 5.599
10. Tang X, Gu X, Ren Z, Ma Y, Lai Y, Peng H*(通讯作者), Peng S, Zhang Y*; Synthesis and evaluation of substituted dibenzo[c,e]azepine-5-ones as P-glycoprotein-mediated multidrug resistance reversal agents. Bioorg Med Chem Lett. 2012; 22(8):2675-80 IF: 2.338
11. Gu X, Ren Z, Tang X, Peng H*(通讯作者), Ma Y, Lai Y, Peng S, Zhang Y*; Synthesis and biological evaluation of bifendate-chalcone hybrids as a new class of potential P-glycoprotein inhibitors. Bioorg Med Chem. 2012; 20(8):2540-8 IF: 2.903
12. Gu X, Ren Z, Tang X, Peng H*(通讯作者), Zhao Q, Lai Y, Peng S, Zhang Y*; Synthesis and biological evaluation of novel bifendate derivatives bearing 6,7-dihydro-dibenzo[c,e] azepine scaffold as potent P-glycoprotein inhibitors. Eur. J. Med. Chem. 2012; 51:137-144. IF: 3.499
13. Tang X, Gu X, Ai H, Wang G, Peng H, Lai Y, Zhang Y; Synthesis and evaluation of nitric oxide-releasing DDB derivatives as potential Pgp-mediated MDR reversal agents in MCF-7/Adr cells. Bioorg Med Chem Lett. 2012; 22(2):801-5 IF: 2.338
14. Chen L, Li Y, Zhao Q, Peng H*(通讯作者), Hou T*; ADME Evaluation in Drug Discovery. 10. Predictions of P-Glycoprotein Inhibitors using Recursive Partitioning and Naïve Bayesian Classification Techniques. Mol Pharmaceutics 2011; 8(3):889-900. IF: 4.782
15. Wei H¶, Lin Z¶, Feng J¶, Peng H, Guo R, Han G, Geng S, Lang X, Sun Y, Shen B, Li Y; Identification of conformational core epitope Lys
16. Li Y, Feng J, Geng S, Geng S, Wei H, Chen G, Li X, Wang L, Wang R, Peng H, Han G, Shen B, Li Y. The N- and C-terminal carbohydrate recognition domains of galectin-9 contribute differently to its multiple functions in innate immunity and adaptive immunity. Mol Immunol. 2011; 48(4):670-7. IF: 2.897
17. Zhang Y, Yang M, Ji Q, Fan D, Peng H, Yang C, Xiong D, Zhou Y; Anoikis induction and metastasis suppression by a new integrin αvβ3 inhibitor in human melanoma cell line M21. Invest New Drugs 2011; 29:666~73 IF: 3.357
18. Wu J, Wang Y, Jia P, Wang C, Zhao Y, Peng H, Wei W, Li H; Immunochromatography detection of ricin in environmental and biological samples. Nano Biomed.
19. Peng H, Qi J, Dong Z, Zhang JT; Dynamic vs Static ABCG2 Inhibitors to Sensitize Drug Resistant Cancer Cells. PLoS ONE 2010; 5(12):e15276 IF: 4.411
20. Peng H, Dong Z, Qi J, Yang Y, Liu Y, Li Z, Xu J, Zhang JT; A Novel Two Mode-Acting Inhibitor of ABCG2-mediated Multidrug Transport and Resistance in Cancer Chemotherapy. PLoS ONE 2009; 4(5):e5676 IF: 4.351
21. Liu Y, Yang Y, Qi J, Peng H, Zhang JT; Effect of cysteine mutagenesis on the function and disulfide bond formation of human ABCG2. J Pharmacol Exp Ther. 2008; 326(1):33-40 IF: 4.309
22. Xu J, Peng H, Zhang JT. Human Multidrug Transporter ABCG2, a Target for Sensitizing Drug Resistance in Cancer Chemotherapy. Curr Med Chem. 2007; 14:689-701 IF: 4.944
23. Xu J, Peng H, Chen Q, Liu Y, Dong Z, Zhang JT; Oligomerization domain of the multidrug resistance-associated transporter ABCG2 and its dominant inhibitory activity. Cancer Res. 2007; 67(9):4373-81 IF: 7.672
24. Yang Y, Liu Y, Dong Z, Xu J, Peng H, Liu Z, Zhang JT; Regulation of function by dimerization through the amino terminal membrane-spanning domain of human ABCC1/MRP1. J Biol Chem. 2007; 282(12):8821-30 IF: 4.773
获奖情况:
1.“血液肿瘤耐药机制及克服耐药研究” (编号:2004JB-1-007)
2005年天津市科技进步一等奖
2.“亲溶酶体剂净化白血病骨髓药物构效关系研究” (编号:2001JB-3-121)
2002年天津市科技进步三等奖
3.“抗CD3和抗CD20双功能抗体的研制” (编号:2001JB-2-029)
2002年天津市科技进步二等奖
联系方式:
联系地址:北京市海淀区太平路27号军科院四所十室,邮编:100850
联系电话:(O),**
Email:p_h2002@hotmail.com