共找到3條詞條名為李敏勇的結果 展開
- 中國台灣學者
- 山東大學教授
- 廈門興才職業技術學院藝術與建築學院副院長
李敏勇
山東大學教授
2000.9 – 2005.6 中國藥科大學藥物化學專業學習,獲理學博士學位;
2003.7 - 2003.9 北京大學天然藥物與仿生藥物國家重點實驗室進行客座研究;
2005.9 – 2007.10 美國喬治亞州立大學(Georgia State University)化學系進行博士后研究工作;
2007.10 – 2009.4美國喬治亞州立大學(Georgia State University)化學系助理教授;
2009.4- 至今 山東大學藥學院藥物化學研究所關鍵崗教授、博士生導師。
李敏勇為American Chemical Society、Cheminformatics and QSAR Society、Sigma Xi, the Scientific Research Society、中國化學會會員和中國藥學會高級會員,曾擔任Chemical Communication、Physical Chemistry Chemical Physics、Molecular BioSystems、Organic & Biomolecular Chemistry、Chemical Biology & Drug Design、Journal of Computational Chemistry、Journal of Molecular Modeling、Journal of Computer-Aided Molecular Design、FEBS Letters、Bioorganic Medicinal Chemistry Letters、Bioorganic Medicinal Chemistry、Journal of Global Infectious Diseases、Journal of Biological Research、Molecules、Journal of Medicinal Plants Research、Letters in Drug Design & Discovery和Drug Design, Development and Therapy等國際學術雜誌審稿人,同時任Current Topics in Medicinal Chemistry雜誌的特邀編委。
2022年3月,藥學院李敏勇教授團隊與基礎醫學院馬春紅教授團隊合作在Journal of the American Chemical Society(中科院JCR一區,IF=15.419)上發表了以“Photophosphatidylserine guides natural killer cells photoimmunotherapyviaTim-3”為題的合作研究成果。
1. 華實海洋藥物獎勵基金管理委員會,首屆華實海洋藥物青年科技獎二等獎,2009
2. ELSEVIER中國科技部,SCOPUS青年科學之星,2009
承擔主要科研項目情況
1. 芳基磺醯類新型抗菌活性化合物的研究,山東省中青年科學家科研獎勵基金(BS2009SW011),5萬,主持,2009.12-2012.12
2. SecA ATPase 抑製劑的抗菌活性研究,高等學校博士學科點專項科研基金(20090131120080),3.6萬,主持,2010.1-2012.12
3. 藥效團與骨架躍遷策略在天然先導優化中的應用研究,霍英東教育基金會高等院校青年教師基金 (122036),2萬美元,主持,2010.5-2013.4
4. AI-2型群體感應抑製劑的抗菌活性研究,國家自然科學基金(81001362),23萬,主持,2011.1-2013.12
6. 分子探針在藥物研究中的應用,山東省自然科學基金傑出青年基金(JQ201019),50萬,主持,2010.10-2013.10
目前已發表60餘篇SCI論文,其中第一或通訊作者有29篇,被SCI引用次數有380餘次,被引用H指數(H index)為13,申請中國、美國和世界專利8項,目前作為課題負責人主持國家自然科學基金、山東省自然科學傑出青年基金、霍英東教育基金會高等院校青年教師基金、教育部博士點專項資金、山東省中青年優秀科學家科技獎勵基金、山東大學自主創新基金自然科學類專項傑出青年基金等多項科研項目,總經費130餘萬元。由於在化學與生命科學領域的突出貢獻,李敏勇教授獲得了2009年“華實海洋藥物青年科技獎”、“SCOPUS青年科學之星”等多項科技獎勵,並多次受邀在國內和國際學術會議上做學術報告。
主編教材及著作
1.《抗腫瘤藥物設計與發現》,化學工業出版社,2017年
3.《計算機輔助藥物設計實驗講義》,內部使用,2013年
1. 基於生物靶標的合理藥物設計、合成及生物活性研究
主要圍繞與疾病相關如AI-2型細菌群體效應受體LuxP、細菌SecA ATPase、α1-腎上腺素能受體、鉀離子通道等生物靶點,以有機化學、藥物化學、計算化學等方法為研究手段,進行基於靶點結構的合理藥物分子設計、合成與生物活性研究。
2. 化學生物學研究
1. Li, M. Y.; Du, L. P.; Wu, B.; Xia, L. Self-organizing molecular field analysis on α1a-adrenoceptor dihydropyridine antagonists. Bioorg. Med. Chem. 2003, 11, 3945-3951.
2. Li, M. Y.; Tsai, K. C.; Xia, L. Pharmacophore identification of α1A-adrenoceptor antagonists. Bioorg. Med. Chem. Lett. 2005, 15, 657-664.
3. Li, M. Y.; Fang, H.; Xia, L. Pharmacophore-based design, synthesis, biological evaluation, and 3D-QSAR studies of aryl-piperazines as α1-adrenoceptor antagonists. Bioorg. Med. Chem. Lett. 2005, 15, 3216-3219.
4. Li, M. Y.; Lu, J. F.; Xia, L. Receptor-based molecular modeling study on antagonist-bound human α1A, α1B and α1D-adrenoceptors. Acta Chim. Sinica 2005, 63, 1875-1883.
5. Li, M. Y.; Wang, B. H. Computational studies of H5N1 hemagglutinin binding with SA-α-2, 3-Gal and SA-α-2, 6-Gal. Biochem. Biophys. Res. Commun. 2006, 347, 662-668. (Top 10 Hottest Articles on Biochemical and Biophysical Research Communications on July – September 2006)
6. Li, M. Y.; Xia, L. Rational design, synthesis, biological evaluation, and structure-activity relationship studies of novel 1-indanone α1-adrenoceptor antagonists. Chem. Biol. Drug Des. 2007, 70, 461-464.
7. Li, M. Y.; Wang, B. H. Homology modeling and examination of the effect of the D92E mutation on the H5N1 nonstructural protein NS1 effector domain. J. Mol. Model. 2007, 13, 1237-1244.
8. Yang, Q.; Wang, Y. J.; Du, L. P.; Li, M. Y.*; You, Q. D. Strategies for atrial fibrillation therapy: focusing on IKur potassium channel. Expert Opin. Ther. Patents 2007, 17, 1443-1456.
9. Li, M. Y.; Huang, Y. J.; Tai, P. C.; Wang, B. H. Discovery of the first SecA inhibitors using structure-based virtual screening. Biochem. Biophys. Res. Commun. 2008, 368, 839-845.
10. Ni, N. T.; Chou, H. T.; Wang, J. F.; Li, M. Y.; Lu, C. D.; Tai, P. C.; Wang, B. H. Identification of boronic acids as antagonists of bacterial quorum sensing in Vibrio harveyi. Biochem. Biophys. Res. Commun. 2008, 369, 590-594.
11. Li, M. Y.*; Ni, N. T.; Wang, B. H.; Zhang, Y. Q. Modeling the excitation wavelengths (λex) of boronic acids. J. Mol. Model. 2008, 14, 441-449.
12. Yang, Q.; Du, L. P.; Wang, X. J.; Li, M. Y.*; You, Q. D. Modeling the binding modes of Kv1.5 potassium channel and blockers. J. Mol. Graph. Model. 2008, 27, 178-187.
13. Li, M. Y.; Ni, N. T.; Chou, H. T.; Lu, C. D.; Tai, P. C.; Wang, B. H. Structure-based discovery and experimental verification of novel Al-2 quorum sensing inhibitors against Vibrio harveyi. ChemMedChem 2008, 3, 1242-1249.
14. Tsai, K. C.; Wang, S. H.; Hsiao, N. W.; Li, M. Y.*; Wang, B. H. The effect of different electrostatic potentials on docking accuracy: A case study using DOCK5.4. Bioorg. Med. Chem. Lett. 2008, 18, 3509-3512.
15. Li, M. Y.*; Fang, H.; Du, L. P.; Xia, L.; Wang, B. H. Computational studies of the binding site of α1A-adrenoceptor antagonists. J. Mol. Model. 2008, 14, 957-966.
16. Li, M. Y.; Lin, N.; Huang, Z.; Du, L. P.; Altier, C.; Fang, H.; Wang, B. H. Selecting aptamers for a glycoprotein through the incorporation of the boronic acid moiety. J. Am. Chem. Soc. 2008, 130, 12636-12638. (Highlighted by Faculty of 1000 Biology)
17. Yang, Q.; Du, L. P.; Wang, X. J.; Li, M. Y.*; You, Q. D. Pharmacophore Mapping for Kv1.5 Potassium Channel Blockers. QSAR Comb. Sci. 2009, 28, 59-71.
18. Li, M. Y.* The medicinal chemistry of ion channels and their relevance in drug discovery. Curr. Top. Med. Chem. 2009, 9, 321.
19. Du, L. P.; Li, M. Y.*; You, Q. D. The interactions between hERG potassium channel and blockers. Curr. Top. Med. Chem. 2009, 9, 330-338.
20. Yang, Q.; Wang, X. J.; Du, L. P.; Li, M. Y.*; You, Q. D. Drug discoveries towards Kv1.5 potassium channel. Curr. Top. Med. Chem. 2009, 9, 339-347.
21. Jin, S., Choudhary, G., Cheng, Y.F., Dai, C.F., Li, M.Y.* and Wang, B.H., Fluoride Protects Boronic Acids in Copper (I)-mediated Click Reaction, Chem. Commun., 2009, 5251-5253.
22. Cheng, Y.F., Li, M.Y.*, Wang, S.R., Peng, H.J., Reid, S., Ni, N.T., Fang, H., Xu, W.F. and Wang, B.H., Carbohydrate Biomarkers for Future Disease Detection and Treatment, Sci. China Chem. 2010, 53, 3-20.
23. Du, L.P., Ni, N.T., Li, M.Y.* and Wang, B.H., A Fluorescent Hydrogen Peroxide Probe Based on a ‘Clickable’ Coumarin Fluorophore, Tetrahedron Lett. 2010, 51, 1152-1154.
24. Tsai, K.C., Wang, S.H., Hsiao, N.W., Li, M.Y.*, and Wang, B.H., A Comparsion of Different Electrostatic Potentials on Prediction Accuracy using CoMFA and CoMSIA Studies, Eur. J. Med. Chem. 2010, 45, 1544-1551.
25. Wang, X.J., Yang, Q., Yin, D.L., Li, M.Y.* and You, Q.D., in silico Binding Characteristics between Human Histamine H1 Receptor and Antagonists, J. Mol. Model., 2010, 16, 1529-1537.
26. Du, L.P. and Li, M.Y. *, Modeling the Interactions Between α1-Adrenergic Receptors and Their Antagonists, Curr. Comput. Aid. Drug Des. 2010, 6, 165-178.
27. Sun, W., Du, L.P. and Li, M.Y.*, Aptamer-based Carbohydrate Recognition, Curr. Pharm. Des., 2010, 16, 2269-2278.
28. King-Keller, S., Li, M.Y., Smith, A., Zheng, S., Kaur, G., Yang, X., Wang, B.H. and Docampo, R. Chemical Validation of Phosphodiesterase C as a Chemotherapeutic Target in Trypanosoma cruzi, the Etiological Agent of Chagas' Disease, Antimicrob. Agents Chemother., 2010, 54, 3738-3745 (co-first author)
29. Yang, Q., Fedida, D., Xu, H., Wang, B., Du, L., Wang, X., Li, M.Y.* and You, Q.D. Structure-Based Virtual Screening and Electrophysiological Evaluation of New Chemotypes of Kv1.5 Channel Blockers, ChemMedChem, 2010, 5, 1353-1358.
30. Gao Y, Lin Y, Liu T, Chen H, Yang X, Tian C, Du L and Li MY.*. A Bioluminescent Probe for Tumor Hypoxia Detection via CYP450 Reductase in Living Animals. Anal. Chem. 2017, 89, 12488-93.
31. Wu W, Su J, Tang C, Bai H, Ma Z, Zhang T, Yuan Z, Li Z, Zhou W, Zhang H, Liu Z, Wang Y, Zhou Y, Du L, Gu L and Li, M.Y.* cybLuc: An Effective Aminoluciferin Derivative for Deep Bioluminescence Imaging. Anal. Chem. 2017, 89, 4808-16.
32. Zhang H, Su J, Lin Y, Bai H, Liu J, Chen H, Du L, Gu L and Li, M.Y.* Inhibiting Firefly Bioluminescence by Chalcone. Anal. Chem. 2017, 89, 6099-6105