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服务平台首页>协同创新>专家库>专家详情

来芳芳(教授)

所属单位:中国医学科学院药物研究所

担任职务:

擅长领域:

联系方式:010-63165207 邮箱:登录后查看

 

来芳芳

 

教育背景

2003.9-2007.7  浙江大学药学院 陈海亮辅导员  本科/理学学士

2007.9-2012.7  北京协和医学院医药生物技术研究所  司书毅研究员  博士(直博)/医学博士

2010.5-2012.5  美国托莱多大学  Zijian Xie 教授  交流访问

 

联系方式

Tel010-63165207

Emaillaifangfang@imm.ac.cn

 

工作经历

2012.8-2016.7    中国医学科学院药物研究所 陈晓光研究员课题组 助理研究员2016.7-至今      中国医学科学院药物研究所 药理系 副高级研究员

 

专业研究领域

主要从事肿瘤和肿瘤免疫学的药理学研究及相应的新药临床前开发。2012年至今共发表SCI论文20余篇,核心期刊5篇;申请专利14项,授权专利2项。近年来主持承担了国家自然科学基金青年基金、药物所基本科研业务费团队建设专项等多个研究项目,并作为主要研究人员参与了协和重大协同创新项目、十三五国家重大科技专项和多项国家自然科学基金面上项目等。参与编写《中国药用植物志》、《中华医学百科全书》等专业书籍3部。作为临床前药效学研究的的主要完成人,正在全程参与研发与申报11.1类新药。

 

发表论文

[1] Y. He, J. Wen, Q. Cui, F. Lai, D. Yin, H. Cui, Quantitative Evaluation of in Vivo Target Efficacy of Anti-tumor Agents via an Immunofluorescence and EdU Labeling Strategy, Front Pharmacol, 9 (2018) 812.

[2] F. Lai, N. Madan, Q. Ye, Q. Duan, Z. Li, S. Wang, S. Si, Z. Xie, Identification of a mutant alpha1 Na/K-ATPase that pumps but is defective in signal transduction, J Biol Chem, 288 (2013) 13295-13304.

[3] Q. Ye, F. Lai, M. Banerjee, Q. Duan, Z. Li, S. Si, Z. Xie, Expression of mutant alpha1 Na/K-ATPase defective in conformational transition attenuates Src-mediated signal transduction, J Biol Chem, 288 (2013) 5803-5814.

[4] F. Lai, Q. Liu, X. Liu, M. Ji, P. Xie, X. Chen, LXY6090 - a novel manassantin A derivative - limits breast cancer growth through hypoxia-inducible factor-1 inhibition, Onco Targets Ther, 9 (2016) 3829-3840.

[5] F. Lai, Z. Shen, H. Wen, J. Chen, X. Zhang, P. Lin, D. Yin, H. Cui, X. Chen, A Morphological identification cell cytotoxicity assay using cytoplasm-localized fluorescent probe (CLFP) to distinguish living and dead cells, Biochem Biophys Res Commun, 482 (2017) 257-263.

[6] Y. Xu, Q. Liu, Y. Xu, C. Liu, X. Wang, X. He, N. Zhu, J. Liu, Y. Wu, Y. Li, N. Li, T. Feng, F. Lai, M. Zhang, B. Hong, J.D. Jiang, S. Si, Rutaecarpine suppresses atherosclerosis in ApoE-/- mice through upregulating ABCA1 and SR-BI within RCT, J Lipid Res, 55 (2014) 1634-1647.

[7] M. Ji, L. Wang, J. Chen, N. Xue, C. Wang, F. Lai, R. Wang, S. Yu, J. Jin, X. Chen, CAT3, a prodrug of 13a(S)-3-hydroxyl-6,7-dimethoxyphenanthro[9,10-b]-indolizidine, circumvents temozolomide-resistant glioblastoma via the Hedgehog signaling pathway, independently of O(6)-methylguanine DNA methyltransferase expression, Onco Targets Ther, 11 (2018) 3671-3684.

[8] M. Ji, L. Wang, N. Xue, F. Lai, S. Zhang, J. Jin, X. Chen, The Development of a Biotinylated NAD(+)-Applied Human Poly(ADP-Ribose) Polymerase 3 (PARP3) Enzymatic Assay, SLAS Discov, 23 (2018) 545-553.

[9] N. Yan, Y. He, H. Wen, F. Lai, D. Yin, H. Cui, A Suzuki-Miyaura method for labelling proliferating cells containing incorporated BrdU, Analyst, 143 (2018) 1224-1233.

[10] F. Niu, Y. Li, F.F. Lai, X.G. Chen, [Research progress of hypoxia-inducible factor 1 inhibitors against tumors], Yao Xue Xue Bao, 49 (2014) 832-836.

[11] J. Miao, H. Cui, J. Jin, F. Lai, H. Wen, X. Zhang, G.F. Ruda, X. Chen, D. Yin, Development of 3-alkyl-6-methoxy-7-hydroxy-chromones (AMHCs) from natural isoflavones, a new class of fluorescent scaffolds for biological imaging, Chem Commun (Camb), 51 (2015) 881-884.

[12] Y. Wang, Q. Ye, C. Liu, J.X. Xie, Y. Yan, F. Lai, Q. Duan, X. Li, J. Tian, Z. Xie, Involvement of Na/K-ATPase in hydrogen peroxide-induced activation of the Src/ERK pathway in LLC-PK1 cells, Free Radic Biol Med, 71 (2014) 415-426.

[13] H. Wen, Q. Cui, H. Meng, F. Lai, S. Wang, X. Zhang, X. Chen, H. Cui, D. Yin, A high-resolution method to assess cell multinucleation with cytoplasm-localized fluorescent probes, Analyst, 141 (2016) 4010-4013.

[14] N. Xue, Q. Zhou, M. Ji, J. Jin, F. Lai, J. Chen, M. Zhang, J. Jia, H. Yang, J. Zhang, W. Li, J. Jiang, X. Chen, Chlorogenic acid inhibits glioblastoma growth through repolarizating macrophage from M2 to M1 phenotype, Sci Rep, 7 (2017) 39011.

[15] L. Yan, F. Lai, X. Chen, Z. Xiao, Discovery of novel indirubin-3'-monoxime derivatives as potent inhibitors against CDK2 and CDK9, Bioorg Med Chem Lett, 25 (2015) 2447-2451.

[16] S. Zhang, D. Wang, N. Xue, F. Lai, M. Ji, J. Jin, X. Chen, Nicousamide protects kidney podocyte by inhibiting the TGFbeta receptor II phosphorylation and AGE-RAGE signaling, Am J Transl Res, 9 (2017) 115-125.

[17] H. Zhao, M. Ji, G. Cui, J. Zhou, F. Lai, X. Chen, B. Xu, Discovery of novel quinazoline-2,4(1H,3H)-dione derivatives as potent PARP-2 selective inhibitors, Bioorg Med Chem, 25 (2017) 4045-4054.

[18] A. Zhou, L. Yan, F. Lai, X. Chen, M. Goto, K.H. Lee, Z. Xiao, Design, synthesis and biological evaluation of novel indolin-2-ones as potent anticancer compounds, Bioorg Med Chem Lett, 27 (2017) 3326-3331.

[19] Y. Xu, F. Lai, Y. Xu, Y. Wu, Q. Liu, N. Li, Y. Wei, T. Feng, Z. Zheng, W. Jiang, L. Yu, B. Hong, S. Si, Mycophenolic acid induces ATP-binding cassette transporter A1 (ABCA1) expression through the PPARgamma-LXRalpha-ABCA1 pathway, Biochem Biophys Res Commun, 414 (2011) 779-782.

[20] F. Niu, Y. Li, F.F. Lai, L. Ni, M. Ji, J. Jin, H.Z. Yang, C. Wang, D.M. Zhang, X.G. Chen, LB-1 Exerts Antitumor Activity in Pancreatic Cancer by Inhibiting HIF-1alpha and Stat3 Signaling, J Cell Physiol, 230 (2015) 2212-2223.

[21] F.F. Lai, F. Niu, H.Z. Yang, W.Q. Zhou, X.G. Chen, [Development of a novel screening assay for inhibitors targeting HIF-1alpha and P300 interaction], Yao Xue Xue Bao, 49 (2014) 849-853.

 

专著

1.《中国药用植物志》,艾铁民 (2016)。 撰写第五卷下册,P915-P964

2.《中华医学百科全书》,张奉春 (2017)。撰写肿瘤学-抗肿瘤生物疗法

 

专利

1、司书毅,许艳妮,刘祺,蒋建东,洪斌,李卓荣,姜威,贺晓波,徐扬,李永臻,来芳芳,巫晔翔,李霓,王智敏,刘伟,吴茱萸次碱类化合物的新用途,授权日期2012.9.26,授权号CN201110067053.1

2、司书毅,张忠兵,刘继开,许艳妮,谢子建,洪斌,姜威,李卓荣,王智敏,来芳芳,刘伟,冯婷婷,人ATP结合盒转运体A1活性调节剂筛选模型及其应用,授权日期2012.10.3,授权号CN201110074634.8

3、冯志强,陈晓光,杨阳,来芳芳,季鸣,张莉婧,郑义,薛妮娜,王克,李凌。苄苯醚类衍生物、及其制法和药物组合物与用途。申请日期:2017.05.23,申请号:PCT/CN2017/085417

4、冯志强,陈晓光,杨阳,郑义,来芳芳,季鸣,周川,张莉婧,王克,薛妮娜,李凌。烟醇醚类衍生物、及其制法和药物组合物与用途。申请日期:2017.05.23,申请号:PCT/CN2017/085418

5、冯志强,陈晓光,张莉婧,杨阳,来芳芳,季鸣,周川,郑义,薛妮娜,李凌。溴代苄醚衍生物、及其制法和药物组合物与用途。申请日期:2017.05.23,申请号:PCT/CN2017/085419

6、冯志强,陈晓光,杨阳,周川,来芳芳,季鸣,金小锋,薛妮娜,郑义,陈浩,李凌。苯醚类衍生物、及其制法和药物组合物与用途。申请日期:2017.05.23,申请号:PCT/CN2017/085420

7、冯志强,陈晓光,杨阳,来芳芳。2-羟基-4-(2,3-双取代苄氧基)-5-取代苯甲醛衍生物的制备方法。申请日期:2017.05.23,申请号:PCT/CN2017/085421

8、冯志强,陈晓光,杨阳,来芳芳,季鸣,张莉婧,郑义,薛妮娜,王克,李凌。苄苯醚类衍生物、及其制法和药物组合物与用途。申请日期:2017.05.23,申请号:2017103656711

9、冯志强,陈晓光,杨阳,郑义,来芳芳,季鸣,周川,张莉婧,王克,薛妮娜,李凌。烟醇醚类衍生物、及其制法和药物组合物与用途。申请日期:2017.05.23 ,申请号:2017103635221

10、冯志强,陈晓光,张莉婧,杨阳,来芳芳,季鸣,周川,郑义,薛妮娜,李凌。溴代苄醚衍生物、及其制法和药物组合物与用途。申请日期:2017.05.23,申请号:2017103656961

11、冯志强,陈晓光,杨阳,周川,来芳芳,季鸣,金小锋,薛妮娜,郑义,陈浩,李凌。苯醚类衍生物、及其制法和药物组合物与用途。申请日期:2017.05.23,申请号:2017103599795

12、冯志强,陈晓光,杨阳,来芳芳。2-羟基-4-(2,3-双取代苄氧基)-5-取代苯甲醛衍生物的制备方法。申请日期:2017.05.23,申请号:2017103635236

13、崔华清、文辉、尹大力、林平、沈政委、陈嘉凌、张翔、来芳芳、陈晓光。丹磺酰胺化合物及其制备方法。申请日期:2015.06.23,申请号:201510679418.4

14、张东明,陈晓光,王超,郎立伟,李创军,来芳芳,牛非。雷醇内酯衍生物及其应用。申请日期:2013.10.08,申请号:201310463847.9

 

 

 

 

 

 

 

 

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