English
新闻公告
More
化学进展 2016, Vol. 28 Issue (9): 1363-1386 DOI: 10.7536/PC160325 前一篇   后一篇

• 综述与评论 •

“精准医疗”背景下的分子靶向药物研究——精准药物设计策略浅析

展鹏, 王学顺, 刘新泳*   

  1. 山东大学药学院 药物化学研究所 化学生物学教育部重点实验室 济南 250012
  • 收稿日期:2016-03-01 修回日期:2016-05-01 出版日期:2016-09-15 发布日期:2016-08-16
  • 通讯作者: 刘新泳 E-mail:xinyongllab@163.com
  • 基金资助:
    国家自然科学基金重点国际合作研究项目(No.81420108027),国家自然科学基金面上项目(No.81573347,81273354),山东大学青年学者未来计划(No.2016WLJH32),山东省重点研发计划(重大关键技术)(No.2015ZDJS04001)和山东省科技发展计划项目(No.2014GSF118012)资助

Contemporary Molecular Targeted Drug in the Context of “Precision Medicine”: An Attempting Discussion of “Precision Drug Design”

Zhan Peng, Wang Xueshun, Liu Xinyong*   

  1. Department of Medicinal Chemistry, Key Laboratory of Chemical Biology(Ministry of Education), School of Pharmaceutical Sciences, Shandong University, Jinan 250012, China
  • Received:2016-03-01 Revised:2016-05-01 Online:2016-09-15 Published:2016-08-16
  • Supported by:
    The work was surpported by the Key Program of the National Natural Science Foundation of China(No. 81420108027),the National Natural Science Foundation of China (No. 81573347,81273354),the Young Scholars Program of Shandong University (YSPSDU No. 2016WLJH32),the Major Project of Science and Technology of Shandong Province(No. 2015ZDJS04001), and the Science and Technology Development Project of Shandong Province(No. 2014GSF118012).
如何实现对肿瘤、病毒感染等严重危害人类健康的疾病的精准治疗是当前医学界的难题和研究热点。随着“精准医疗”计划的启动,当代药物设计也随之进入“精准”靶向药物分子设计时代。基于靶标结构的合理药物设计及特异性的药物递送系统是当代精准药物设计的重要方面。靶标-配体精准相互作用为基于靶标的合理药物设计奠定了理论基础;精准“制导”化学合成方法学的研究为药物合成提供了强有力的工具;灵敏、准确分子探针的研究为当代化学生物学及发现特异性的药物递送系统提供有效的辅助手段。本文从以上几方面,从药物化学的视角综述了“精准医疗”背景下的分子靶向诊疗药物研究。
How to cure serious diseases which do harm to the health of human being such as tumor and virus infection by "precision medicine" is always a difficult problem and a research hotspot in the medical field. With the launch of "precision medicine" project, contemporary drug design has reached the new era, namely, "precise" targeted drug molecular design should be one of the key pillars of precision medicine. The structure-based rational drug design and the targeted drug delivery system are important aspects of the contemporary "precision drug design". Precise noncovalent interactions between ligands and proteins lay the theoretical foundations for structure-based rational drug design. The development of new synthetic methodologies provides a powerful tool for drug precise synthesis, focusing both on the identification of intrinsically novel reactions, as well as the discovery of improved methods for carrying out existing transformations. Chemical biology has a significant role to play in the discovery and validation of new therapeutic targets. Over the past few years, many sensitive and accurate probes based on small organic molecules have demonstrated considerable promise in "precision drug design" as they provide a chemoproteomic means to confirm and quantify target engagement and selectivity of small molecule drug candidates. In the viewpoint of medicinal chemistry, this review highlights recent advances made in contemporary molecular targeted drug design in the context of "precision medicine".

Contents
1 Introduction
2 Structure-based "precision drug design"
2.1 Target-specific drug design
2.2 Isoform-selective drug design
2.3 Drug design strategies to overcome drug resistance
3 Kinetic target-guided dynamic combina-toril chemistry
4 Precise noncovalent interactions between ligands and proteins
5 The development of new synthetic methodologies:late stage functionalization of drug-like molecules
6 Targeted drug precise delivery systems
6.1 Biomarker-based drug precise delivery systems
6.2 Microenvironment-based drug precise delivery systems
6.3 Drug precise delivery systems based on organ-specific enzymes
6.4 Organelle-targeted drug precise delivery systems:mitochondria
6.5 Photodynamic therapy
7 Probes:chemical biology tools for "precision drug design"
7.1 Peptides-based probes
7.2 H2O2 probes
7.3 H2S probes
7.4 Thiol-mediated cleavable fluorescent probles
7.5 Fluoride probes
7.6 Cysteamine two-photon fluorescence probes
7.7 Photo-triggered probes
7.8 MAO-B-specific probes
7.9 Biotin-based probes and diagnostic reagents
8 Conclusions and outlook

中图分类号: 

()
[1] 何明燕(He M Y), 夏景林(Xia J L), 王向东(Wang X D). 世界临床药物(World Clinical Drugs), 2015, (06):418.
[2] Collins F S, Varmus H. N. Engl. J. Med., 2015, 372(9):793.
[3] 汤立达(Tang L D), 徐为人(Xu W R). 现代药物与临床(Drugs & Clinic), 2015, 4:351.
[4] Poot A J, van Ameijde J, Slijper M, van den Berg A, Hilhorst R, Ruijtenbeek R, Rijkers D T, Liskamp R M. Chembiochem., 2009, 10:2042.
[5] van Wandelen L T, van Ameijde J, Mady A S, Wammes A E, Bode A, Poot A J, Ruijtnbeek R, Liskamp R M. ChemMedChem., 2012, 7:2113.
[6] Volkamer A, Eid S, Turk S, Rippmann F, Fulle S. J. Chem. Inf. Model., 2016, 56:335.
[7] Song Y, Zhan P, Li X, Rai D, de Clercq E, Liu X. Curr. Med. Chem., 2013, 20:815.
[8] Lucas M C, Goldstein D M, Hermann J C, Kuglstatter A, Liu W, Luk K C, Padilla F, Slade M, Villaseñor A G, Wanner J, Xie W, Zhang X, Liao C. J. Med. Chem., 2012, 55:10414.
[9] Melillo B, Liang S Y, Park J, Schon A, Courter J R, LaLonde J M, Wendler D J, Princiotto A M, Seaman M S, Freire E, Sodroski J, Madani N, Hendrickson W A, Smith A B. ACS Med. Chem. Lett., 2016, 7:330.
[10] Zhan P, Itoh Y, Suzuki T, Liu X. J. Med. Chem., 2015, 58:7611.
[11] Folkes A J, Ahmadi K, Alderton W K, Alix S, Baker S J, Box G, Chuckowree I S, Clarke P A, Depledge P, Eccles S A, Friedman L S, Hayes A, Hancox T C, KugendradasA, Lensun L, Moore P, Olivero A G, Pang J, Patel S, Pergl-Wilson G H, Raynaud F I, Robson A, Saghir N, Salphati L, Sohal S, Ultsch M H, Valenti M, Wallweber H J, Wan N C, Wiesmann C, Workman P, Zhyvoloup A, Zvelebil M J, Shuttleworth S J. J. Med. Chem., 2008, 51:5522.
[12] Nacht M, Qiao L, Sheets M P, St Martin T, Labenski M, Mazdiyasni H, Karp R, Zhu Z, Chaturvedi P, Bhavsar D, Niu D, Westlin W, Petter R C, Medikonda A P, Singh J. J. Med. Chem., 2013, 56:712.
[13] Schr der J, Klinger A, Oellien F, Marh fer R J, Duszenko M, Selzer P M. J. Med. Chem., 2013, 56:1478.
[14] Pinson J A, Zheng Z, Miller M S, Chalmers D K, Jennings I G, Thompson P E. ACS Med. Chem. Lett., 2013, 4:206.
[15] Jaime-Figueroa S, de Vicente J, Hermann J, Jahangir A, Jin S, Kuglstatter A, Lynch SM, Menke J, Niu L, Patel V, Shao A, Soth M, Vu M D, Yee C. Bioorg. Med. Chem. Lett., 2013, 23:2522.
[16] Zhu J, Yang Q, Dai D, Huang Q. J. Am. Chem. Soc., 2013, 135:11708.
[17] Shao Y X, Huang M, Cui W, Feng L J, Wu Y, Cai Y, Li Z, Zhu X Liu P, Wan Y, Ke H, Luo H B. J. Med. Chem., 2014, 57:10304.
[18] Yao Y, Chen P, Diao J, Cheng G, Deng L, Anglin J L, Prasad B V, Song Y. J. Am. Chem. Soc., 2011, 133:16746.
[19] Wang X, Huang B, Suzuki T, Liu X, Zhan P. Epigenomics., 2015, 7:1379.
[20] Ogasawara D, Itoh Y, Tsumoto H, Kakizawa T, Mino K, Fukuhara K, Nakagawa H, Hasegawa M, Sasaki R, Mizukami T, Miyata N, Suzuki T. Angew. Chem. Int. Ed. Engl., 2013, 52:8620.
[21] Ranganathan A, Stoddart L A, Hill S J, Carlsson J. J. Med. Chem., 2015, 58:9578.
[22] Wada Y, Shirahashi H, Iwanami T, Ogawa M, Nakano S, Morimoto A, Kasahara K, Tanaka E, Takada Y, Ohashi S, Mori M, Shuto S. J. Med. Chem., 2015, 58:6048.
[23] Yoon H, Kwak Y, Choi S, Cho H, Kim N D, Sim T. J. Med. Chem., 2016, 59:358.
[24] Zhan P, Pannecouque C, de Clercq E, Liu X. J. Med. Chem., 2016, 59:2849.
[25] Zhan P, Chen X, Li D, Fang Z, de Clercq E, Liu X. Med. Res. Rev., 2013, 33:E1.
[26] Zhan P, Liu X, Li Z, Pannecouque C, de Clercq E. Curr. Med. Chem., 2009, 16:3903.
[27] Kang D, Song Y, Chen W, Zhan P, Liu X. Mol. Biosyst., 2014, 10:1998.
[28] Song Y, Fang Z, Zhan P, Liu X. Curr. Med. Chem., 2014, 21:329.
[29] Campiani G, Nacci V, Fiorini I, de Filippis M P, Garofalo A, Greco G, Novellino E, Altamura S, di Renzo L. J. Med. Chem., 1996, 39:26720.
[30] Campiani G, Morelli E, Fabbrini M, Nacci V, Greco G, Novellino E, Ramunno A, Maga G, Spadari S, Caliendo G, Bergamini A, Faggioli E, Uccella I, Bolacchi F, Marini S, Coletta M, Nacca A, Caccia S. J. Med. Chem., 1999, 42:4462.
[31] Fattorusso C, Gemma S, Butini S, Huleatt P, Catalanotti B, Persico M, de Angelis M, Fiorini I, Nacci V, Ramunno A, Rodriquez M, Greco G, Novellino E, Bergamini A, Marini S, Coletta M, Maga G, Spadari S, Campiani G. J. Med. Chem., 2005, 48:7153.
[32] Zanoli S, Gemma S, Butini S, Brindisi M, Joshi B P, Campiani G, Fattorusso C, Persico M, Crespan E, Cancio R, Spadari S, Hübscher U, Maga G. Biochem. Pharmacol., 2008, 76:156.
[33] Butini S, Brindisi M, Cosconati S, Marinelli L, Borrelli G, Coccone S S, Ramunno A, Campiani G, Novellino E, Zanoli S, Samuele A, Giorgi G, Bergamini A, Di Mattia M, Lalli S, Galletti B, Gemma S, Maga G. J. Med. Chem., 2009, 52(4):1224.
[34] Zhan P, Li Z, Liu X, de Clercq E. Mini. Rev. Med. Chem., 2009, 9:1014.
[35] Li W, Li X, De Clercq E, Zhan P, Liu X. Eur. J. Med. Chem., 2015, 102:167.
[36] O'Meara J A, Jakalian A, LaPlante S, Bonneau P R, Coulombe R, Faucher A M, Guse I, Landry S, Racine J, Simoneau B, Thavonekham B, Yoakim C. Bioorg. Med. Chem. Lett., 2007, 17:3362.
[37] Gagnon A, Amad M H, Bonneau P R, Coulombe R, de Roy P L, Doyon L, Duan J, Garneau M, Guse I, Jakalian A, Jolicoeur E, Landry S, Malenfant E, Simoneau B, Yoakim C. Bioorg. Med. Chem. Lett., 2007, 17:4437.
[38] Hopkins A L, Ren J, Tanaka H, Baba M, Okamato M, Stuart D I, Stammers D K. J. Med. Chem., 1999, 42:4500.
[39] Cheng H, Nair S K, Murray B W, Almaden C, Bailey S, Baxi S, Behenna D C, Cho-Schultz S, Dalvie D, Dinh D M, Edwards M P, Feng J L, Ferre R, Gajiwala K S, Hemkens M D, Jackson-Fisher A, Jalaie M, Johnson T O, Kania R S, Kephart S, Lafontaine J A, Lunney E, Liu K K, Liu Z, Matthews J, Nagata A, Niessen S, Ornelas M A, Orr S T, Pairish M, Planken S, Ren S, Richter D T, Ryan K, Sach N W, Shen H, Smeal T, Solowiej J, Sutton S C, Tran K, Tseng E, Vernier W F, Walls M, Wang S, Weinrich S L, Xin S, Xu H, Yin M J, Zhou R, Zientek M, Kath J. J. Med. Chem., 2016, 59:2005.
[40] Engel J, Lategahn J, Rauh D. ACS Med. Chem. Lett., 2015, 7:2.
[41] Hu X, Manetsch R. Chem. Soc. Rev., 2010, 39(4):1316.
[42] Mamidyala S K, Finn M G. Chem. Soc. Rev., 2010, 39:1252.
[43] Sharpless K B, Manetsch R. Expert. Opin. Drug. Discov., 2006, 1:525.
[44] Corbett P T, Leclaire J, Vial L, West K R, Wietor J L, Sanders J K, Otto S. Chem. Rev., 2006, 106:3652.
[45] Wang X, Huang B, Liu X, Zhan P. Drug. Discov. Today., 2016, 21:118.
[46] Hu X, Sun J, Wang H G, Manetsch R. J. Am. Chem. Soc., 2008, 130:13820.
[47] Kulkarni S S, Hu X, Doi K, Wang H G, Manetsch R. ACS Chem. Biol., 2011, 6:724.
[48] Lu Y, Shi T, Wang Y, Yang H, Yan X, Luo X, Jiang H, Zhu W. J. Med. Chem., 2009, 52:2854.
[49] Lu Y, Liu Y, Xu Z, Li H, Liu H, Zhu W. Expert. Opin. Drug. Discov., 2012, 7:375.
[50] Lu Y, Wang Y, Xu Z, Yan X, Luo X, Jiang H, Zhu W. J. Phys. Chem. B., 2009, 113:12615.
[51] Lu Y, Wang Y, Zhu W. Phys. Chem. Chem. Phys., 2010, 12:4543.
[52] Ren J, He Y, Chen W, Chen T, Wang G, Wang Z, Xu Z, Luo X, Zhu W, Jiang H, Shen J, Xu Y. J. Med. Chem., 2014, 57:3588.
[53] Cernak T, Dykstra K D, Tyagarajan S, Vachal P, Krska S W. Chem. Soc. Rev., 2016, 45:546.
[54] Toutov A A, Liu W B, Betz K N, Stoltz B M, Grubbs R H. Nat. Protoc., 2015, 10:1897.
[55] Sharma A, Hartwig J F. Nature, 2015, 517:600.
[56] Wu N, Song F, Yan L, Li J, You J. Chemistry, 2014, 20:3408.
[57] Dai H X, Stepan A F, Plummer M S, Zhang Y H, Yu J Q. J. Am. Chem. Soc., 2011, 133:7222.
[58] Yamaguchi A D, Chepiga K M, Yamaguchi J, Itami K, Davies H M. J. Am. Chem. Soc., 2015, 137:644.
[59] He J, Hamann L G, Davies H M, Beckwith R E. Nat. Commun., 2015, 6:5943.
[60] Hong B, Li C, Wang Z, Chen J, Li H, Lei X. J. Am. Chem. Soc., 2015, 137:11946.
[61] Fox J C, Gilligan R E, Pitts A K, Bennett H R, Gaunt M J. Chem. Sci., 2016, 7:2706.
[62] Gayakhe V, Sanghvi Y S, Fairlamb I J, Kapdi A R. Chem. Commun (Camb)., 2015, 51:11944.
[63] Sekizawa H, Amaike K, Itoh Y, Suzuki T, Itami K, Yamaguchi J. ACS Med. Chem.Lett., 2014, 5:582.
[64] Liu Y J, Xu H, Kong W J, Shang M, Dai H X, Yu J Q. Nature, 2014, 515:389.
[65] Zhang F L, Hong K, Li T J, Park H, Yu JQ. Science., 2016, 351:252.
[66] Légaré M A, Courtemanche M A, Rochette É, Fontaine F G. Science., 2015, 349:513.
[67] Miyamura S, Araki M, Suzuki T, Yamaguchi J, Itami K. Angew. Chem. Int. Ed. Engl., 2015, 54:846.
[68] Saadi J, Wennemers H. Nature Chemistry, 2016, 8:276.
[69] Jaracz S, Chen J, Kuznetsova L V, Ojima I. Bioorg. Med. Chem., 2005, 13:5043.
[70] 李安良(Li A L), 李正香(Li Z X). 中国药学杂志(Chinese Pharmaceutical Journal)., 2003, 4:3.
[71] Burkhart D J, Barthel B L, Post G C, Kalet B T, Nafie J W, Shoemaker R K, Koch T H. J. Med. Chem., 2006, 49:7002.
[72] Barthel B L, Zhang Z, Rudnicki D L, Coldren C D, Polinkovsky M, Sun H, Koch G G, Chan D C, Koch T H. J. Med. Chem., 2009, 52:7678.
[73] Barthel B L, Rudnicki D L, Kirby T P, Colvin S M, Burkhart D J, Koch T H. J. Med. Chem., 2012, 55:6595.
[74] Leu Y L, Chen C S, Wu Y J, Chern J W. J. Med. Chem., 2008, 51:1740.
[75] Wei G, Loktionova N A, Pegg A E, Moschel R C. J. Med. Chem., 2005, 48:256.
[76] Brady S F, Pawluczyk J M, Lumma P K, Feng D M, Wai J M, Jones R, de Feo-Jones D, Wong B K, Miller-Stein C, Lin J H, Oliff A, Freidinger R M, Garsky V M. J. Med. Chem., 2002, 45:4706.
[77] de Feo-Jones D, Brady S F, Feng D M, Wong B K, Bolyar T, Haskell K, Kiefer D M, Leander K, McAvoy E, Lumma P, Pawluczyk J M, Wai J, Motzel S L, Keenan K, van Zwieten M, Lin J H, Garsky V M, Freidinger R, Oliff A, Jones R E. Mol. Cancer. Ther., 2002, 1:451.
[78] 梁旭华(Liang X H), 樊君(Fan J), 孙洋(Sun Y), 谭春雷(Fan C L). 中国新药杂志(Chinese Journal of New Drugs), 2012, 22:2647.
[79] 付利强(Fu L Q), 丁实(Ding S), 杨玉社(Yang Y S). 中国药物化学杂志(Chinese Journal of Medicinal Chemistry), 2013, 3:226.
[80] 王中领(Wang Z L), 郭亮(Guo L). 临床放射学杂志(Journal of Clinical Radiology), 2014, 1:143.
[81] Vlahov I R, Santhapuram H K, Kleindl P J, Howard S J, Stanford K M, Leamon C P. Bioorg. Med. Chem. Lett., 2006, 16:5093.
[82] Vlahov I R, Leamon C P. Bioconjug. Chem., 2012, 23:1357.
[83] Vlahov I R, Vite G D, Kleindl P J, Wang Y, Santhapuram H K, You F, Howard S J, Kim S H, Lee F F, Leamon C P. Bioorg. Med. Chem. Lett., 2010, 20:4578.
[84] Leamon C P, Reddy J A, Vlahov I R, Westrick E, Dawson A, Dorton R, Vetzel M, Santhapuram H K, Wang Y. Mol. Pharm., 2007, 4:659.
[85] Liu P, Xu J, Yan D, Zhang P, Zeng F, Li B, Wu S. Chem. Commun (Camb)., 2015, 51:9567.
[86] 杜钢军(Du G J), 时小燕(Shi X Y). 国际药学研究杂志(International Journal of Pharmaceutical Research), 2011, 5:336.
[87] 张慈安(Zhang C A), 魏品康(Wei P K), 李勇进(Li Y J). 肿瘤(Tumor), 2010, 6:550.
[88] Kuang Y, Balakrishnan K, Gandhi V, Peng X. J. Am. Chem. Soc., 2011, 133:19278.
[89] Kim E J, Bhuniya S, Lee H, Kim H M, Cheong C, Maiti S, Hong K S, Kim J S. J. Am. Chem. Soc., 2014, 136:13888.
[90] Park S, Kim E, Kim W Y, Kang C, Kim J S. Chem. Commun (Camb)., 2015, 51:9343.
[91] Erion M D, van Poelje P D, Mackenna D A, Colby T J, Montag A C, Fujitaki J M, Linemeyer D L, Bullough D A. J. Pharmacol. Exp. Ther., 2005, 312:554.
[92] Zhang Q, Milliken P, Kulczynska A, Slawin A M, Gordon A, Kirkby N S, Webb D J, Botting N P, Megson I L. J. Med. Chem., 2013, 56:5321.
[93] Juillerat-Jeanneret L, Flohr A, Schneider M, Walter I, Wyss J C, Kumar R, Golshayan D, Aebi J D. J. Med. Chem., 2015, 58:8097.
[94] Hochd rffer K, Abu Ajaj K, Schäfer-Obodozie C, Kratz F. J. Med. Chem., 2012, 55:7502.
[95] Lehoux D, Ostiguy V, Fadhil I, Laquerre K, Tanaka K S E, Kang T, Lafontaine Y, Houghton T J, Reddy R, Moeck G, Rafai Far A, Parr Jr T R. 18th European Congress of Clinical Microbiology and Infectious Diseases Barcelona, Spain. 2008.
[96] 瞿鼎(Qu D). 第四军医大学硕士论文(Master's Dissertation of Fourth Military Medical University), 2010.
[97] 齐倩倩(Qi Q Q), 贺艺超(He Y C), 肖典(Xiao D), 周辛波(Zhou X B), 赵国明(Zhao G M). 国际药学研究杂志(International Journal of Pharmaceutical Research), 2012, 39:460.
[98] Brewster M E, Anderson W R, Webb A I, Pablo L M, Meinsma D, Moreno D, Derendorf H, Bodor N, Pop E. Antimicrob Agents Chemother., 1997, 41:122.
[99] Berezovskaia IuV, Chudinov M V. Bioorg. Khim., 2005, 31:339.
[100] 潘凌立(Pan L L), 潘达(Pan D), 廖卫兵(Liao W B), 柯超(Ke C), 陈安清(Chen A Q), 郭清莲(Guo Q L). 医学综述(Medical Recapitulate), 2015, 1:37.
[101] 齐雪静(Qi X J), 郑楠楠(Zheng N N), 高亚男(Gao Y N), 吴琳华(Wu L H), 唐景玲(Tang J L). 中国药学杂志(Chinese Pharmaceutical Journal), 2015, 9:741.
[102] 张李巧(Zhang L Q). 中国医院药学杂志(Chinese Journal of Hospital Pharmacy), 2015, 24:2257.
[103] Sharpe M A, Han J, Baskin A M, Baskin D S. ChemMedChem., 2015, 10:621.
[104] Horbert R, Pinchuk B, Davies P, Alessi D, Peifer C. ACS Chem. Biol., 2015, 10:2099.
[105] Jones L H. Future. Med. Chem., 2015, 7:2131.
[106] Chowdhury M A, Moya I A, Bhilocha S, McMillan C C, Vigliarolo B G, Zehbe I, Phenix C P. J. Med. Chem., 2014, 57:6092.
[107] Lo L C, Chu C Y. Chem. Commun (Camb)., 2003, 21:2728.
[108] Carroll V, Michel B W, Blecha J, VanBrocklin H, Keshari K, Wilson D, Chang C J. J. Am. Chem. Soc., 2014, 136:14742.
[109] van de Bittner G C, Dubikovskaya E A, Bertozzi C R, Chang C J. Proc. Natl. Acad. Sci. U S A., 2010, 107(50):21316.
[110] Xu J, Zhang Y, Yu H, Gao X, Shao S. Anal. Chem., 2016, 88:1455.
[111] Narayanaswamy N, Narra S, Nair R R, Saini D K, Kondaiah P, Govindaraju T. Chem. Sci., 2016, 7:2832.
[112] Lin V S, Chen W, Xian M, Chang C J. Chem. Soc. Rev., 2015, 44:4596.
[113] Lee M H, Sessler J L, Kim J S. Acc. Chem. Res., 2015, 48:2935.
[114] Lee M H, Kim J Y, Han J H, Bhuniya S, Sessler J L, Kang C, Kim J S. J. Am.Chem. Soc., 2012, 134:12668.
[115] Bhuniya S, Maiti S, Kim E J, Lee H, Sessler J L, Hong K S, Kim J S. Angew. Chem. Int. Ed. Engl., 2014, 53:4469.
[116] Maiti S, Park N, Han J H, Jeon H M, Lee J H, Bhuniya S, Kang C, Kim J S. J. Am. Chem. Soc., 2013, 135:4567.
[117] Bhuniya S, Lee M H, Jeon H M, Han J H, Lee J H, Park N, Maiti S, Kang C, Kim J S. Chem. Commun (Camb)., 2013, 49:7141.
[118] 姜娜(Jiang N), 樊江莉(Fan J L), 杨洪宝(Yang H B), 彭孝军(Peng X J). 化工学报(Journal of Chemical Industry and Engineering(China)), 2016, 67:176.
[119] Lim C S, Masanta G, Kim H J, Han J H, Kim H M, Cho B R. J. Am. Chem. Soc., 2011, 133:11132.
[120] Yamamoto J, Maeda N, Komiya C, Tanaka T, Denda M, Ebisuno K, Nomura W, Tamamura H, Sato Y, Yamauchi A, Shigenaga A, Otaka A. Tetrahedron, 2014, 70:5122.
[121] Gu J A, Mani V, Huang S T. Analyst., 2015, 140:346.
[122] Sarkar A R, Heo C H, Kim E, Lee H W, Singh H, Kim J J, Kang H, Kang C, Kim H M. Chem. Commun (Camb)., 2015, 51:2407.
[123] Jung D, Sato K, Min K, Shigenaga A, Jung J, Otaka A, Kwon Y. Chem. Commun (Camb)., 2015, 51:9670.
[124] Furutani M, Uemura A, Shigenaga A, Komiya C, Otaka A, Matsuura K. Chem. Commun (Camb)., 2015, 51:8020.
[125] Li L, Zhang C W, Chen G Y, Zhu B, Chai C, Xu Q H, Tan E K, Zhu Q, Lim K L, Yao S Q. Nat. Commun., 2014, 5:3276.
[126] Li L, Zhang C W, Ge J, Qian L, Chai B H, Zhu Q, Lee J S, Lim K L, Yao S Q. Angew. Chem. Int. Ed. Engl., 2015, 54:10821.
[127] Vineberg J G, Wang T, Zuniga E S, Ojima I. J. Med. Chem., 2015, 58:2406.
[128] Peck R W. Nat. Rev. Drug. Discov., 2016, 15:145.
[129] 展鹏(Zhan P), 刘新泳(Liu X Y). 中国科技论文(China Sciencepaper), 2015, 10:2140.
[130] Tavassoli A. Future Med. Chem., 2015, 7:2089.
[131] 张艳(Zhang Y), 陈鹏(Chen P), 姚祝军(Yao Z J). 科学通报(Chinese Science Bulletin), 2013, 58:2872.
[132] Xie X S. JAMA., 2015, 313:2021.
[133] 杜建(Du J), 唐小利(Tang X L). 中国科学基金(Bulletin of National Natural Science Foundation of China), 2016, 1:20.
[1] 傅安辰, 毛彦佳, 王宏博, 曹志娟. 基于二氧杂环丁烷骨架的化学发光探针发展和应用研究[J]. 化学进展, 2023, 35(2): 189-205.
[2] 赖燕琴, 谢振达, 付曼琳, 陈暄, 周戚, 胡金锋. 基于1,8-萘酰亚胺的多分析物荧光探针的构建和应用[J]. 化学进展, 2022, 34(9): 2024-2034.
[3] 李立清, 郑明豪, 江丹丹, 曹舒心, 刘昆明, 刘晋彪. 基于邻苯二胺氧化反应的生物分子比色/荧光探针[J]. 化学进展, 2022, 34(8): 1815-1830.
[4] 周宇航, 丁莎, 夏勇, 刘跃军. 荧光探针在半胱氨酸检测的应用[J]. 化学进展, 2022, 34(8): 1831-1862.
[5] 颜范勇, 臧悦言, 章宇扬, 李想, 王瑞杰, 卢贞彤. 检测谷胱甘肽的荧光探针[J]. 化学进展, 2022, 34(5): 1136-1152.
[6] 赵惠, 胡文博, 范曲立. 双光子荧光探针在生物传感中的应用[J]. 化学进展, 2022, 34(4): 815-823.
[7] 王学川, 王岩松, 韩庆鑫, 孙晓龙. 有机小分子荧光探针对甲醛的识别及其应用[J]. 化学进展, 2021, 33(9): 1496-1510.
[8] 李斌, 付艳艳, 程建功. 检测有机磷神经毒剂及模拟物的荧光探针[J]. 化学进展, 2021, 33(9): 1461-1472.
[9] 任春平, 聂雯, 冷俊强, 刘振波. 反应型次氯酸荧光探针[J]. 化学进展, 2021, 33(6): 942-957.
[10] 侯晓涵, 刘胜男, 高清志. 小分子荧光探针在绿色农药开发中的应用[J]. 化学进展, 2021, 33(6): 1035-1043.
[11] 党耶城, 冯杨振, 陈杜刚. 红光/近红外光硫醇荧光探针[J]. 化学进展, 2021, 33(5): 868-882.
[12] 吴云雪, 张衡益, 刘育. 偶氮苯衍生物探针在乏氧细胞成像中的应用[J]. 化学进展, 2021, 33(3): 331-340.
[13] 刘园园, 郭芸, 罗晓刚, 刘根炎, 孙琦. 近红外荧光探针检测金属离子、小分子和生物大分子[J]. 化学进展, 2021, 33(2): 199-215.
[14] 刘加伟, 王婧, 王其, 范曲立, 黄维. 激活型有机光声造影剂的应用[J]. 化学进展, 2021, 33(2): 216-231.
[15] 徐云雪, 刘仁发, 徐坤, 戴志飞. 手术导航用荧光探针[J]. 化学进展, 2021, 33(1): 52-65.