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An esterase-cleavable persulfide donor with no electrophilic byproducts and a fluorescence reporter

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dc.contributor.author CHOUDHARY, BHARAT S. en_US
dc.contributor.author KUMAR, T. ANAND en_US
dc.contributor.author Vashishtha, Akshi en_US
dc.contributor.author TEJASRI, SUSHMA en_US
dc.contributor.author KUMAR, AMAL S. en_US
dc.contributor.author Agarwal, Rachit en_US
dc.contributor.author CHAKRAPANI, HARINATH en_US
dc.date.accessioned 2024-01-30T05:10:09Z
dc.date.available 2024-01-30T05:10:09Z
dc.date.issued 2024-01 en_US
dc.identifier.citation Chemical Communications en_US
dc.identifier.issn 1359-7345 en_US
dc.identifier.issn 1364-548X en_US
dc.identifier.uri https://doi.org/10.1039/D3CC04948E en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8432
dc.description.abstract Hydrogen sulfide (H2S) and associated sulfur species known as persulfide or sulfane sulfur are considered among the first responders to oxidative stress. However, tools that reliably generate these species without any potentially toxic byproducts are limited, and even fewer report the generation of a persulfide. Here, using a latent fluorophore embedded with N-acetylcysteine persulfide, we report a new tool that is cleaved by esterase to produce a persulfide as well as a fluorescence reporter without any electrophilic byproducts. The rate of formation of the fluorescence reporter is nearly identical to the rate of formation of the persulfide suggesting that the use of this probe eliminates the need for secondary assays that report persulfide formation. Symptomatic with persulfide generation, the newly developed donor was able to protect chondrocyte cells from oxidative stress. en_US
dc.language.iso en en_US
dc.publisher Royal Society of Chemistry en_US
dc.subject Activation en_US
dc.subject Sulfide en_US
dc.subject 2024-JAN-WEEK2 en_US
dc.subject TOC-JAN-2024 en_US
dc.subject 2024 en_US
dc.title An esterase-cleavable persulfide donor with no electrophilic byproducts and a fluorescence reporter en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Chemical Communications en_US
dc.publication.originofpublisher Foreign en_US


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