Please use this identifier to cite or link to this item: https://doi.org/10.1039/c6sc01643j
Title: Fluorescent transmembrane anion transporters: Shedding light on anionophoric activity in cells
Authors: Berry, S.N
Soto-Cerrato, V
Howe, E.N.W
Clarke, H.J
Mistry, I
Tavassoli, A
Chang, Y.-T 
Pérez-Tomás, R
Gale, P.A
Keywords: Cell membranes
Cytology
Fluorescence
Ion exchange
Ions
Metabolism
Transport properties
Urea
Antineoplastic agents
Cancer cells
Fluorescence studies
Fluorinated compound
Naphthalimide
Shedding light
Thiourea groups
Transmembranes
Cells
Issue Date: 2016
Publisher: Royal Society of Chemistry
Citation: Berry, S.N, Soto-Cerrato, V, Howe, E.N.W, Clarke, H.J, Mistry, I, Tavassoli, A, Chang, Y.-T, Pérez-Tomás, R, Gale, P.A (2016). Fluorescent transmembrane anion transporters: Shedding light on anionophoric activity in cells. Chemical Science 7 (8) : 5069-5077. ScholarBank@NUS Repository. https://doi.org/10.1039/c6sc01643j
Rights: Attribution 4.0 International
Abstract: A series of fluorescent anion transporters consisting of a urea or thiourea group linked to a naphthalimide fluorophore have been synthesised and their anion transport properties studied. The compounds possess similar anion transport properties to (thio)urea-based anionophores that have previously been reported. Fluorescence studies in cells show all anionophores cross the plasma membrane and localise within the interior of cells. The most lipophilic, aromatic substituted transporters localise homogeneously throughout the cell and are toxic towards cancer cells with the highly fluorinated compound 6 being the most effective. The least lipophilic, alkyl substituted transporters localise in specific vesicles and are non-toxic to cells. This work provides new insight to the actions of anionophores in cells and may be useful in the design of novel antineoplastic agents. © The Royal Society of Chemistry 2016.
Source Title: Chemical Science
URI: https://scholarbank.nus.edu.sg/handle/10635/180391
ISSN: 2041-6520
DOI: 10.1039/c6sc01643j
Rights: Attribution 4.0 International
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