Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5231
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dc.contributor.authorCHAUHAN, DINESH PRATAPSINHen_US
dc.contributor.authorSAHA, TANMOYen_US
dc.contributor.authorLAHIRI, MAYURIKAen_US
dc.contributor.authorTALUKDAR, PINAKIen_US
dc.date.accessioned2020-10-20T07:07:33Z-
dc.date.available2020-10-20T07:07:33Z-
dc.date.issued2014-01en_US
dc.identifier.citationTetrahedron Letters, 55(1), 244-247.en_US
dc.identifier.issn0040-4039en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5231-
dc.identifier.urihttps://doi.org/10.1016/j.tetlet.2013.11.003en_US
dc.description.abstractThe design, synthesis, and photophysical properties of new BODIPY-based fluorogenic ‘click on’ dyes are reported. CuAAC reaction of non-fluorescent BODIPY azide with a series of non-fluorescent alkyne molecules resulted in fluorescent triazoles which displayed up to 532-fold enhancement of fluorescence in the red region. Imaging studies confirmed the general trend of cell permeability and a cholesterol linked derivative exhibited selective localization into intracellular membranes.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.subjectBODIPYen_US
dc.subjectAzide-alkyne click reactionen_US
dc.subjectFluorescenceen_US
dc.subjectSolvatochromic propertiesen_US
dc.subjectCell imagingen_US
dc.subject2014en_US
dc.titleBODIPY based 'click on' fluorogenic dyes: application in live cell imagingen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Biologyen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleTetrahedron Lettersen_US
dc.publication.originofpublisherForeignen_US
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