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research article

Perfluorinated HDAC inhibitors as selective anticancer agents

Walton, James W.
•
Cross, Jasmine M.
•
Riedel, Tina  
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2017
Organic & Biomolecular Chemistry

A series of potent histone deacetylase inhibitors is presented that incorporate alkyl or perfluorinated alkyl chains. Several new compounds show greater in vitro antiproliferative activity than the clinically approved inhibitor, SAHA. Furthermore, the new compounds show up to 5-fold greater activity against cancer cells than healthy cells. This selectivity is in contrast to SAHA, which is more active against the healthy cell line than the cancer cell line tested. Finally, we report an increase in activity for SAHA under mild hyperthermia, indicating that it could be an interesting candidate to use in combination with thermal therapy.

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Type
research article
DOI
10.1039/c7ob02339a
Web of Science ID

WOS:000414805900019

Author(s)
Walton, James W.
Cross, Jasmine M.
Riedel, Tina  
Dyson, Paul J.  
Date Issued

2017

Publisher

Royal Society of Chemistry

Published in
Organic & Biomolecular Chemistry
Volume

15

Issue

43

Start page

9186

End page

9190

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LCOM  
Available on Infoscience
December 4, 2017
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/142554
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