| Literature DB >> 27094621 |
Yen Leng Pak1, Jun Li1, Kyoung Chul Ko2, Gyoungmi Kim1, Jin Yong Lee2, Juyoung Yoon1.
Abstract
In this study, we developed a turn-on mitochondria-targeting hydrogen sulfide, "probe 1", based on the selective thiolysis of 7-nitro-1,2,3-benzoxadiazole amine moiety attached to the piperazine-based naphthalimide scaffold. Probe 1 exhibited excellent properties with 68-fold fluorescence enhancement, a low detection limit (2.46 μM), a low cytotoxicity, and a good selectivity toward hydrogen sulfide. The success of intracellular imaging indicated that probe 1 could be used in further applications for the investigation of biological functions and pathological roles of H2S in living systems.Entities:
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Year: 2016 PMID: 27094621 DOI: 10.1021/acs.analchem.6b00956
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986