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Conjugated structures based on quinazolinones and their application in fluorescent labeling
As an alkaloid, quinazolinone exhibits excellent biological properties; structurally, it also has the potential to construct fluorescent probes with conjugated structures. In this work, probes 5a-c and 6b were obtained by introducing quinazolone into aldehydes with different numbers of double bonds....
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Published in: | Organic & biomolecular chemistry 2023-03, Vol.21 (9), p.1992-2 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | As an alkaloid, quinazolinone exhibits excellent biological properties; structurally, it also has the potential to construct fluorescent probes with conjugated structures. In this work, probes
5a-c
and
6b
were obtained by introducing quinazolone into aldehydes with different numbers of double bonds. Their absorption maxima were located at 420-540 nm and their emission maxima were at 500-600 nm in solvents of different polarities. In particular, probe
5c
showed significant fluorescence enhancement with the increase in viscosity due to the limited intramolecular rotation, and its fluorescence intensity in glycerol was 37.8 times higher than that in water. Moreover, probes
5a-c
and
6b
containing the N
H
structure showed sensitive response to pH, and their fluorescence intensity in alkaline solution (pH 9-11) was suddenly enhanced, which was elucidated with the help of theoretical calculation. In addition, the cell experiments showed that probes
5a
and
5b
had the ability to target mitochondria and probes
5c
and
6b
targeted lysosomes in HeLa cells. Furthermore, the viscosity-sensitive probe
5c
could be used for monitoring changes in lysosomal viscosity in HeLa cells, which had important guiding significance for designing multi-response fluorogenic probes and promoting the advancement of cancer diagnosis.
Four probes containing quinoxalinone were designed and synthesized for self-targeting different organelles in HeLa cells. |
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ISSN: | 1477-0520 1477-0539 |
DOI: | 10.1039/d2ob02293a |