The Synthesis and Biological Evaluation of Some C-9 and C-10 Substituted Derivatives of the RNA Polymerase I Transcription Inhibitor CX-5461
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Amarasiri, Madushani Chathurika Kumari
VO, Yen Thi-Hoang
Gardiner, Michael
Poh, Perlita
Soo, Priscilla
Pavy, Megan
Hein, Nadine
Ferreira, Rita
Hannan, Kate
Hannan, Ross
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CSIRO Publishing
Abstract
The regio-isomeric alkynyl-substituted derivatives, 2 and 3, of the RNA Polymerase I (Pol I) transcription inhibitor CX-5461 (1) were prepared and the active one (compound 3) subjected to click reactions ([3 + 2]-cycloaddition reactions) with certain alkyl azides bearing biotin or fluorescent tags. Compounds 2 and 3, as well as four [3 + 2]-cycloadducts of the latter, were subjected to biological evaluation in a human acute myeloid leukemia cell line model. Among the six compounds tested only alkyne 3 remained active but this was less potent than parent 1.
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Australian Journal of Chemistry
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2099-12-31
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