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<title lang=en>Synthesis and biological properties of galactofuranosyl-containing fluorescent dyes</title>
<creator>Legentil, Laurent</creator>
<creator>Belaz, Sorya</creator>
<creator>Gangneux, Jean-Pierre</creator>
<creator>Robert-Gangneux, Florence</creator>
<creator>Ferrières, Vincent</creator>
<contributor>Institut des Sciences Chimiques de Rennes (ISCR) ; Université de Rennes 1 (UR1) - Ecole Nationale Supérieure de Chimie de Rennes - Institut National des Sciences Appliquées (INSA) - Centre National de la Recherche Scientifique (CNRS)</contributor>
<contributor>Institut de recherche, santé, environnement et travail [Rennes] (Irset) ; Université d'Angers (UA) - Université des Antilles et de la Guyane (UAG) - Université de Rennes 1 (UR1) - École des Hautes Études en Santé Publique [EHESP] (EHESP) - Institut National de la Santé et de la Recherche Médicale (INSERM) - Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )</contributor>
<contributor>Service de Parasitologie-Mycologie [Rennes] ; Université de Rennes 1 (UR1) - Hôpital Pontchaillou - CHU Pontchaillou [Rennes]</contributor>
<description>International audience</description>
<source>Bioorganic & Medicinal Chemistry Letters</source>
<identifier>hal-01446721</identifier>
<identifier>https://hal-univ-rennes1.archives-ouvertes.fr/hal-01446721</identifier>
<source>https://hal-univ-rennes1.archives-ouvertes.fr/hal-01446721</source>
<source>Bioorganic & Medicinal Chemistry Letters, 2017, 27 (2), pp.152-155. 〈10.1016/j.bmcl.2016.11.090〉</source>
<identifier>PUBMED : 27956346</identifier>
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<identifier>DOI : 10.1016/j.bmcl.2016.11.090</identifier>
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<language>en</language>
<subject>[CHIM] Chemical Sciences</subject>
<type>info:eu-repo/semantics/article</type>
<type>Journal articles</type>
<description lang=en>Two fluorescent galactofuranosides were synthesized and their biological activities evaluated on non-infected and Leishmania infected macrophages. Both tagged scaffolds were able to penetrate macrophages. Compared to the activity of the parent octyl galactofuranoside used as a reference, the fluorescein-conjugate showed altered biological properties while the rhodamine 6G one synergistically acted with the lipid chain to significantly increase antiparasitic activity.</description>
<date>2017</date>
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