Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1930
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dc.contributor.authorJain, Deepak R.en_US
dc.contributor.authorGANESH, KRISHNA N.en_US
dc.date.accessioned2019-02-25T09:00:43Z
dc.date.available2019-02-25T09:00:43Z
dc.date.issued2014-07en_US
dc.identifier.citationJournal of Organic Chemistry, 79(14), 6708-6714.en_US
dc.identifier.issn0022-3263en_US
dc.identifier.issn1520-6904en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1930-
dc.identifier.urihttps://doi.org/10.1021/jo500834uen_US
dc.description.abstractSynthesis, 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.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectFluorescent Derivativesen_US
dc.subjectPeptide Nucleic Aciden_US
dc.subjectDNA Hybridizationen_US
dc.subjectCell Penetration Studiesen_US
dc.subjectCarboxyfluoresceinen_US
dc.subjectNuclear membraneen_US
dc.subject2014en_US
dc.titleClickable Cγ-Azido(methylene/butylene) Peptide Nucleic Acids and Their Clicked Fluorescent Derivatives: Synthesis, DNA Hybridization Properties, and Cell Penetration Studiesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleJournal of Organic Chemistryen_US
dc.publication.originofpublisherForeignen_US
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