Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4146
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dc.contributor.authorCHAUHAN, PREETIen_US
dc.contributor.authorGupta, Kavyaen_US
dc.contributor.authorRAVIKUMAR, GOVINDANen_US
dc.contributor.authorSaini, Deepak Kumaren_US
dc.contributor.authorCHAKRAPANI, HARINATHen_US
dc.date.accessioned2019-10-23T08:48:20Z
dc.date.available2019-10-23T08:48:20Z
dc.date.issued2019-12en_US
dc.identifier.citationChemistry-An Asian Journal, 14(24).en_US
dc.identifier.issn1861-4728en_US
dc.identifier.issn1861-471Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4146-
dc.identifier.urihttps://doi.org/10.1002/asia.201901148en_US
dc.description.abstractThe emergence of hydrogen sulfide (H2S) as an important signalling molecule in redox biology with therapeutic potential has triggered interest in generating this molecule within cells. One strategy that has been proposed is to use carbonyl sulfide (COS) as a surrogate for hydrogen sulfide. Small molecules that generate COS have been shown to produce hydrogen sulfide in the presence of carbonic anhydrase, a widely prevalent enzyme. However, other studies have indicated that COS may have biological effects which are distinct from H2S. Thus, it would be useful to develop tools to compare (and contrast) effects of COS and H2S. Here we report enzyme?activated COS donors that are capable of inducing protein persulfidation, which is symptomatic of generation of hydrogen sulfide. The COS donors are also capable of mitigating stress induced by elevated reactive oxygen species. Together, our data suggests that the effects of COS parallel that of hydrogen sulfide, laying the foundation for further development of these donors as possible therapeutic agents.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectCarbonyl Sulfideen_US
dc.subjectHydrogen Sulfideen_US
dc.subjectPersulfidationen_US
dc.subjectProdrugen_US
dc.subjectTOC-OCT-2019en_US
dc.subject2019en_US
dc.titleCarbonyl Sulfide (COS) Donor Induced Protein Persulfidation Protects against Oxidative Stressen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemistry-An Asian Journalen_US
dc.publication.originofpublisherForeignen_US
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