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Literature DB >> 23295243

A turn-on fluorescent sensor for the discrimination of cystein from homocystein and glutathione.

Li-Ya Niu¹, Ying-Shi Guan, Yu-Zhe Chen, Li-Zhu Wu, Chen-Ho Tung, Qing-Zheng Yang.

Abstract

We report a turn-on fluorescent sensor based on nitrothiophenolate boron dipyrromethene (BODIPY) derivatives for the discrimination of cystein (Cys) from homocystein (Hcy) and glutathione (GSH). The sensor was applied for detection of Cys in living cells.

Entities: Chemical Disease

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Year: 2013 PMID： 23295243 DOI： 10.1039/c2cc38429a

Source DB: PubMed Journal: Chem Commun (Camb) ISSN： 1359-7345 Impact factor: 6.222

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Cited

12 in total

1. Synthesis and spectroscopic properties of β,β'-dibenzo-3,5,8-triaryl-BODIPYs.

Authors: Qianli Meng; Frank R Fronczek; M Graça H Vicente
Journal: New J Chem Date: 2016-02-08 Impact factor: 3.591

2. The fluorescence regulation mechanism of the paramagnetic metal in a biological HNO sensor.

Authors: Wenjing Yang; Xuebo Chen; Huizhen Su; Weihai Fang; Yong Zhang
Journal: Chem Commun (Camb) Date: 2015-06-14 Impact factor: 6.222

3. A fluorescence and UV/vis absorption dual-signaling probe with aggregation-induced emission characteristics for specific detection of cysteine.

Authors: Ruru Li; Xiaoyu Huang; Guolin Lu; Chun Feng
Journal: RSC Adv Date: 2018-07-05 Impact factor: 4.036

4. A dual emission fluorescent probe enables simultaneous detection of glutathione and cysteine/homocysteine.

Authors: Xiao-Feng Yang; Qian Huang; Yaogang Zhong; Zheng Li; Hua Li; Mark Lowry; Jorge O Escobedo; Robert M Strongin
Journal: Chem Sci Date: 2014-06-01 Impact factor: 9.825

5. Preparation of a cyanine-based fluorescent probe for highly selective detection of glutathione and its use in living cells and tissues of mice.

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Journal: Nat Protoc Date: 2015-10-15 Impact factor: 13.491

6. Exploring cysteine regulation in cancer cell survival with a highly specific "Lock and Key" fluorescent probe for cysteine.

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Journal: Chem Sci Date: 2019-09-07 Impact factor: 9.825

7. Rational design of a "dual lock-and-key" supramolecular photosensitizer based on aromatic nucleophilic substitution for specific and enhanced photodynamic therapy.

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Journal: Chem Sci Date: 2020-08-25 Impact factor: 9.825