Quinoline-based tetrazolium prochelators: formazan release, iron sequestration, and antiproliferative efficacy in cancer cells
Name:
Quin_Tetrazolium_Chem Comm_202 ...
Embargo:
2025-05-28
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1.525Mb
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PDF
Description:
Final Accepted Manuscript
Affiliation
Department of Chemistry and Biochemistry, The University of ArizonaIssue Date
2024-05-28
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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 CommunicationsRights
© 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 2024ISSN
1359-7345EISSN
1364-548XVersion
Final accepted manuscriptSponsors
National Institutes of Healthae974a485f413a2113503eed53cd6c53
10.1039/d4cc01523a