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    Quinoline-based tetrazolium prochelators: formazan release, iron sequestration, and antiproliferative efficacy in cancer cells

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    Name:
    Quin_Tetrazolium_Chem Comm_202 ...
    Size:
    1.525Mb
    Format:
    PDF
    Description:
    Final Accepted Manuscript
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    Author
    Sung, Yu-Shien
    Tomat, Elisa
    Affiliation
    Department of Chemistry and Biochemistry, The University of Arizona
    Issue Date
    2024-05-28
    
    Metadata
    Show full item record
    Publisher
    Royal Society of Chemistry (RSC)
    Citation
    Sung, Y. S., & Tomat, E. (2024). Quinoline-based tetrazolium prochelators: formazan release, iron sequestration, and antiproliferative efficacy in cancer cells. Chemical Communications.
    Journal
    Chemical Communications
    Rights
    © 2024 The Royal Society of Chemistry.
    Collection Information
    This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
    Abstract
    Iron-binding strategies in anticancer drug design target the key role of iron in cancer growth. The incorporation of a quinoline moiety in the design of tetrazolium-based prochelators facilitates their intracellular reduction/activation to iron-binding formazans. The new prochelators are antiproliferative at submicromolar levels, induce apoptosis and cell cycle arrest, and impact iron signaling in cancer cells.
    Note
    12 month embargo; first published 28 May 2024
    ISSN
    1359-7345
    EISSN
    1364-548X
    DOI
    10.1039/d4cc01523a
    Version
    Final accepted manuscript
    Sponsors
    National Institutes of Health
    ae974a485f413a2113503eed53cd6c53
    10.1039/d4cc01523a
    Scopus Count
    Collections
    UA Faculty Publications

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