Citation: Zhang Shengrui, Wang Qin, Yang Jiajun, Yang Xiao-Feng, Li Zheng, Li Hua. A photocalibrated NO donor based on N-nitrosorhodamine 6G upon UV irradiation[J]. Chinese Chemical Letters, ;2019, 30(2): 454-456. doi: 10.1016/j.cclet.2018.03.011 shu

A photocalibrated NO donor based on N-nitrosorhodamine 6G upon UV irradiation

Zhang Shengrui ^a,b ,
Wang Qin ^a,b ,
Yang Jiajun ^c ,
Yang Xiao-Feng ^a,*, ,
Li Zheng ^c ,
Li Hua ^d,*,

a.
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi'an 710127, China
b.
Shaanxi Key Laboratory of Catalysis, School of Chemistry and Environment Science, Shaanxi University of Technology, Hanzhong 723000, China
c.
College of Life Sciences, Northwest University, Xi'an 710069, China
d.
College of Chemistry and Chemical Engineering, Xi'an Shiyou University, Xi'an 710065, China

xfyang@nwu.edu.cn

Huali@nwu.edu.cn

Received Date: 12 January 2018
Revised Date: 5 March 2018
Accepted Date: 6 March 2018
Available Online: 9 February 2018

Figures(4)

A photocalibrated NO donor, N-nitrosated rhodamine 6G acid (NOG) was designed for monitoring the kinetics or the dose of NO release in a real-time fashion with spectroscopic methods Upon irradiation, a drastic fluorescence turn-on was observed, and the NO release from NOG was not interfered by biothiols. Furthermore, this NO donor enabled time- and site-controlled NO release in living cells. With these merits, NOG can be a useful molecular tool in NO biology.
- Photocalibrated,
- UV irradiation,
- NO donor,
- R6G acid,
- Fluorescence
1. [1]
  J.G. Umans, R. Levi, Annu. Rev. Physiol. 57(1995) 771-790. doi: 10.1146/annurev.ph.57.030195.004011
2. [2]
  D.M. Lloyd-Jones, K.D. Bloch, Annu. Rev. Med. 47(1996) 365-375. doi: 10.1146/annurev.med.47.1.365
3. [3]
  D. Fukumura, S. Kashiwagi, R.K. Jain, Nat. Rev. Cancer 6(2006) 521-534. doi: 10.1038/nrc1910
4. [4]
  J.S. Stamler, Cell 78(1994) 931-936. doi: 10.1016/0092-8674(94)90269-0
5. [5]
  J.W. Jung, K. Damodar, J.K. Kim, et al., Chin. Chem. Lett. 28(2017) 1114-1118. doi: 10.1016/j.cclet.2016.12.041
6. [6]
  D.A. Wink, Y. Vodovotz, J. Laval, et al., Carcinogenesis 19(1998) 711-721. doi: 10.1093/carcin/19.5.711
7. [7]
  L.A. Ridnour, D.D. Thomas, S. Donzelli, et al., Antioxid. Redox Sign. 8(2006) 1329-1337. doi: 10.1089/ars.2006.8.1329
8. [8]
  T. Yamamoto, R.J. Bing, P. Soc. Exp. Biol. Med. 225(2000) 200-206. doi: 10.1046/j.1525-1373.2000.22525.x
9. [9]
  K. Hishikawa, H. Nakagawa, T. Furuta, et al., J. Am. Chem. Soc.131(2009) 7488-7489. doi: 10.1021/ja8093668
10. [10]
  P.T. Burks, J.V. Garcia, R. GonzalezIrias, et al., J. Am. Chem. Soc. 135(2013) 18145-18152. doi: 10.1021/ja408516w
11. [11]
  J.A. Hrabie, J.R. Klose, D.A. Wink, et al., J. Org. Chem. 58(1993) 1472-1476. doi: 10.1021/jo00058a030
12. [12]
  N.L. Fry, P.K. Mascharak, Acc. Chem. Res. 44(2011) 289-298. doi: 10.1021/ar100155t
13. [13]
  H. Okuno, N. Ieda, Y. Hotta, et al., Org. Biomol. Chem. 15(2017) 2791-2796. doi: 10.1039/C7OB00245A
14. [14]
  Z.Q. Zhang, J.Y. Wu, Z.H. Shang, et al., Anal. Chem. 88(2016) 7274-7280. doi: 10.1021/acs.analchem.6b01603
15. [15]
  X.L. Xie, J.L. Fan, M.W. Liang, et al., Chem. Commun. 53(2017) 11941-11944. doi: 10.1039/C7CC06820D
16. [16]
  H.H. He, Z.W. Ye, Y. Xiao, et al., Anal. Chem. 90(2018) 2164-2169. doi: 10.1021/acs.analchem.7b04510
17. [17]
  H.H. He, Z.W. Ye, Y. Zheng, et al., Chem. Commun. 54(2018) 2842-2845. doi: 10.1039/C7CC08886H
18. [18]
  H.N. Kim, M.H. Lee, H.J. Kim, et al., Chem. Soc. Rev. 37(2008) 1465-1472. doi: 10.1039/b802497a
19. [19]
  S. Ma, L. Li, M. She, et al., Chin. Chem. Lett. 28(2017) 2014-2018. doi: 10.1016/j.cclet.2017.09.027
20. [20]
  X.M. Li, R.R. Zhao, Y.L. Wei, et al., Chin. Chem. Lett. 27(2016) 813-816. doi: 10.1016/j.cclet.2016.04.001
21. [21]
  T.A. Grover, J.A. Ramseyer, L.H. Piette, Free Radic. Biol. Med. 3(1987) 27-32. doi: 10.1016/0891-5849(87)90036-0
22. [22]
  K. Piech, T. Bally, A. Sikora, et al., J. Am. Chem. Soc. 129(2007) 3211-3217. doi: 10.1021/ja066855e
23. [23]
  M. Tanno, S. Sueyoshi, N. Miyata, et al., Chem. Pharm. Bull. 45(1997) 595-598. doi: 10.1248/cpb.45.595
24. [24]
  D.A. Wink, J.A. Cook, S.Y. Kim, et al., J. Biol. Chem. 272(1997) 11147-11151. doi: 10.1074/jbc.272.17.11147
25. [25]
  A. Balcerczyk, M. Soszynski, G. Bartosz, Free Radic. Biol. Med. 39(2005) 327-335. doi: 10.1016/j.freeradbiomed.2005.03.017
1. [1]
  Ying Xu , Chengying Shen , Hailong Yuan , Wei Wu . Mapping multiple phases in curcumin binary solid dispersions by fluorescence contrasting. Chinese Chemical Letters, 2024, 35(9): 109324-. doi: 10.1016/j.cclet.2023.109324
2. [2]
  Ying Wang , Hong Yang , Caixia Zhu , Qing Hong , Xuwen Cao , Kaiyuan Wang , Yuan Xu , Yanfei Shen , Songqin Liu , Yuanjian Zhang . Cascading oxidoreductases-like nanozymes for high selective and sensitive fluorescent detection of ascorbic acid. Chinese Chemical Letters, 2025, 36(4): 110153-. doi: 10.1016/j.cclet.2024.110153
3. [3]
  Deshuai Zhen , Chunlin Liu , Qiuhui Deng , Shaoqi Zhang , Ningman Yuan , Le Li , Yu Liu . A review of covalent organic frameworks for metal ion fluorescence sensing. Chinese Chemical Letters, 2024, 35(8): 109249-. doi: 10.1016/j.cclet.2023.109249
4. [4]
  Manman Ou , Yunjian Zhu , Jiahao Liu , Zhaoxuan Liu , Jianjun Wang , Jun Sun , Chuanxiang Qin , Lixing Dai . Polyvinyl alcohol fiber with enhanced strength and modulus and intense cyan fluorescence based on covalently functionalized graphene quantum dots. Chinese Chemical Letters, 2025, 36(2): 110510-. doi: 10.1016/j.cclet.2024.110510
5. [5]
  Junqing Wu , Yiyang Zhang , Qingqing Hong , Hui Yang , Lifeng Zhang , Ming Zhang , Lei Yu . Organometallic modification of silica with europium endowing the fluorescence properties: The key technique for numerical quality monitoring. Chinese Chemical Letters, 2025, 36(4): 110165-. doi: 10.1016/j.cclet.2024.110165
6. [6]
  Zhiwei Zhong , Yanbin Huang , Wantai Yang . A simple photochemical method for surface fluorination using perfluoroketones. Chinese Chemical Letters, 2024, 35(5): 109339-. doi: 10.1016/j.cclet.2023.109339
7. [7]
  Kuan Deng , Fei Yang , Zhi-Qi Cheng , Bi-Wen Ren , Hua Liu , Jiao Chen , Meng-Yao She , Le Yu , Xiao-Gang Liu , Hai-Tao Feng , Jian-Li Li . Construction of wavelength-tunable DSE quinoline salt derivatives by regulating the hybridization form of the nitrogen atom and intramolecular torsion angle. Chinese Chemical Letters, 2024, 35(10): 109464-. doi: 10.1016/j.cclet.2023.109464
8. [8]
  Mengfan Zhang , Lingyan Liu , Peng Wei , Wei Feng , Tao Yi . A proximity tagging strategy utilizing an activated aldehyde group as the active site. Chinese Chemical Letters, 2025, 36(4): 110127-. doi: 10.1016/j.cclet.2024.110127
9. [9]
  Ren Shen , Yanmei Fang , Chunxiao Yang , Quande Wei , Pui-In Mak , Rui P. Martins , Yanwei Jia . UV-assisted ratiometric fluorescence sensor for one-pot visual detection of Salmonella. Chinese Chemical Letters, 2025, 36(4): 110143-. doi: 10.1016/j.cclet.2024.110143
10. [10]
  YanYuan Jia , Rong Rong , Jie Liu , Jing Guo , GuoYu Jiang , Shuo Guo . Unity is Strength, and Independence Shines: A Science Popularization Experiment on AIE and ACQ Effects. University Chemistry, 2024, 39(9): 349-358. doi: 10.12461/PKU.DXHX202402035
11. [11]
  Qin Li , Kexin Yang , Qinglin Yang , Xiangjin Zhu , Xiaole Han , Tao Huang . Illuminating Chlorophyll: Innovative Chemistry Popularization Experiment. University Chemistry, 2024, 39(9): 359-368. doi: 10.3866/PKU.DXHX202309059
12. [12]
  Zehua Zhang , Haitao Yu , Yanyu Qi . 多重共振TADF分子的设计策略. Acta Physico-Chimica Sinica, 2025, 41(1): 2309042-. doi: 10.3866/PKU.WHXB202309042
13. [13]
  Feng Lu , Tao Wang , Qi Wang . Preparation and Characterization of Water-Soluble Silver Nanoclusters: A New Design and Teaching Practice in Materials Chemistry Experiment. University Chemistry, 2025, 40(4): 375-381. doi: 10.12461/PKU.DXHX202406005
14. [14]
  Guixu Pan , Zhiling Xia , Ning Wang , Hejia Sun , Zhaoqi Guo , Yunfeng Li , Xin Li . Preparation of high-efficient donor-π-acceptor system with crystalline g-C3N4 as charge transfer module for enhanced photocatalytic hydrogen evolution. Chinese Journal of Structural Chemistry, 2024, 43(12): 100463-100463. doi: 10.1016/j.cjsc.2024.100463
15. [15]
  Ao Sun , Zipeng Li , Shuchun Li , Xiangbao Meng , Zhongtang Li , Zhongjun Li . Stereoselective synthesis of α-3-deoxy-D-manno-oct-2-ulosonic acid (α-Kdo) derivatives using a C3-p-tolylthio-substituted Kdo fluoride donor. Chinese Chemical Letters, 2025, 36(3): 109972-. doi: 10.1016/j.cclet.2024.109972
16. [16]
  Zhixiao Xiong , Shanni Qiu , Yuyu Wang , Houna Duan , Yi Xiao , Yufang Xu , Weiping Zhu , Xuhong Qian . Photocalibrated NO release from the zinc ion fluorescent probe based on naphthalimide and its application in living cells. Chinese Chemical Letters, 2025, 36(4): 110002-. doi: 10.1016/j.cclet.2024.110002
17. [17]
  Wenya Jiang , Jianyu Wei , Kuan-Guan Liu . Atomically precise superatomic silver nanoclusters stabilized by O-donor ligands. Chinese Journal of Structural Chemistry, 2024, 43(9): 100371-100371. doi: 10.1016/j.cjsc.2024.100371
18. [18]
  Lu LIU , Huijie WANG , Haitong WANG , Ying LI . Crystal structure of a two-dimensional Cd(Ⅱ) complex and its fluorescence recognition of p-nitrophenol, tetracycline, 2, 6-dichloro-4-nitroaniline. Chinese Journal of Inorganic Chemistry, 2024, 40(6): 1180-1188. doi: 10.11862/CJIC.20230489
19. [19]
  Kaimin WANG , Xiong GU , Na DENG , Hongmei YU , Yanqin YE , Yulu MA . Synthesis, structure, fluorescence properties, and Hirshfeld surface analysis of three Zn(Ⅱ)/Cu(Ⅱ) complexes based on 5-(dimethylamino) isophthalic acid. Chinese Journal of Inorganic Chemistry, 2024, 40(7): 1397-1408. doi: 10.11862/CJIC.20240009
20. [20]
  Rong-Nan Yi , Wei-Min He . Electron donor-acceptor complex enabled arylation of dithiocarbamate anions with thianthrenium salts under aqueous micellar conditions. Chinese Chemical Letters, 2024, 35(11): 110194-. doi: 10.1016/j.cclet.2024.110194

Get Citation

PDF

XML

Metrics

PDF Downloads(2)
Abstract views(740)
HTML views(31)

通讯作者: 陈斌, bchen63@163.com

1.
沈阳化工大学材料科学与工程学院沈阳 110142