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Clickable Cγ-Azido(methylene/butylene) Peptide Nucleic Acids and Their Clicked Fluorescent Derivatives: Synthesis, DNA Hybridization Properties, and Cell Penetration Studies

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dc.contributor.author Jain, Deepak R. en_US
dc.contributor.author GANESH, KRISHNA N. en_US
dc.date.accessioned 2019-02-25T09:00:43Z
dc.date.available 2019-02-25T09:00:43Z
dc.date.issued 2014-07 en_US
dc.identifier.citation Journal of Organic Chemistry, 79(14), 6708-6714. en_US
dc.identifier.issn 0022-3263 en_US
dc.identifier.issn 1520-6904 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1930
dc.identifier.uri https://doi.org/10.1021/jo500834u en_US
dc.description.abstract Synthesis, characterization, and DNA complementation studies of clickable Cγ-substituted methylene (azm)/butylene (azb) azido PNAs show that these analogues enhance the stability of the derived PNA:DNA duplexes. The fluorescent PNA oligomers synthesized by their click reaction with propyne carboxyfluorescein are seen to accumulate around the nuclear membrane in 3T3 cells. en_US
dc.language.iso en en_US
dc.publisher American Chemical Society en_US
dc.subject Fluorescent Derivatives en_US
dc.subject Peptide Nucleic Acid en_US
dc.subject DNA Hybridization en_US
dc.subject Cell Penetration Studies en_US
dc.subject Carboxyfluorescein en_US
dc.subject Nuclear membrane en_US
dc.subject 2014 en_US
dc.title Clickable Cγ-Azido(methylene/butylene) Peptide Nucleic Acids and Their Clicked Fluorescent Derivatives: Synthesis, DNA Hybridization Properties, and Cell Penetration Studies en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Journal of Organic Chemistry en_US
dc.publication.originofpublisher Foreign en_US


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