Photoinduced Ring-Opening and Phototoxicity of an Indolin-3-one Derivative
The study of a fluorescent indolin-3-one derivative is reported that, as opposed to its previously described congeners, selectively undergoes photoactivated ring-opening in apolar solvents. The excited state involved in this photoisomerization was partially deactivated by the formation of singlet ox...
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Published in | Chemistry : a European journal Vol. 29; no. 59; p. e202300864 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
WEINHEIM
Wiley
12.09.2023
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | The study of a fluorescent indolin-3-one derivative is reported that, as opposed to its previously described congeners, selectively undergoes photoactivated ring-opening in apolar solvents. The excited state involved in this photoisomerization was partially deactivated by the formation of singlet oxygen. Cell studies revealed lipid droplet accumulation and efficient light-induced cytotoxicity. |
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Bibliography: | Vinnova Swedish Research Council ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0947-6539 1521-3765 1521-3765 |
DOI: | 10.1002/chem.202300864 |