Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4391
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dc.contributor.authorMALWAL, SATISH R.en_US
dc.contributor.authorPARDESHI, KUNDANSINGH A.en_US
dc.contributor.authorCHAKRAPANI, HARINATHen_US
dc.date.accessioned2020-01-31T04:40:08Z
dc.date.available2020-01-31T04:40:08Z
dc.date.issued2020-04en_US
dc.identifier.citationChemBioChem, 21(8), 1201-1205.en_US
dc.identifier.issn1439-7633en_US
dc.identifier.issn1439-4227en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4391
dc.identifier.urihttps://doi.org/10.1002/cbic.201900614en_US
dc.description.abstractAlthough sulfur dioxide (SO2) finds widespread use in the food industry as its hydrated sulfite form, a number of aspects of SO2 biology remain to be completely understood. Of the tools available for intracellular enhancement of SO2 levels, most suffer from poor cell permeability and a lack of control over SO2 release. We report 1,2-cyclic sulfite diesters as a new class of reliable SO2 donors that dissociate in buffer through nucleophilic displacement to produce SO2 with tunable release profiles. We provide data in support of the suitability of these SO2 donors to enhance intracellular SO2 levels more efficiently than sodium bisulfite, the most commonly used SO2 donor for cellular studies.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectCyclic sulfite estersen_US
dc.subjectNucleophilic substitutionen_US
dc.subjectSubstituent effectsen_US
dc.subjectSulfitesen_US
dc.subjectsulfur dioxideen_US
dc.subjectTOC-JAN-2020en_US
dc.subject2020en_US
dc.titleSynthesis of Cyclic Sulfite Diesters and their Evaluation as Sulfur Dioxide (SO2) Donorsen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemBioChemen_US
dc.publication.originofpublisherForeignen_US
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