Reactive cyclic intermediates in the ProTide prodrugs activation: trapping the elusive pentavalent phosphorane
Author:
Affiliation:
1. Institute of Organic Chemistry and Biochemistry
2. Czech Academy of Sciences
3. 166 10 Prague 6
4. Czech Republic
5. Department of Organic Chemistry
6. Faculty of Science
7. Charles University
8. 128 43 Prague 2
Abstract
A combination of NMR and IRPD spectroscopy confirmed the existence of predicted cyclic phosphorus intermediates involved in ProTide prodrugs activation.
Funder
Akademie Věd České Republiky
H2020 European Research Council
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2019/OB/C8OB02870B
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1. Aryl Phosphoramidate Derivatives of d4T Have Improved Anti-HIV Efficacy in Tissue Culture and May Act by the Generation of a Novel Intracellular Metabolite
2. Tenofovir alafenamide: A novel prodrug of tenofovir for the treatment of Human Immunodeficiency Virus
3. Sofosbuvir, a Significant Paradigm Change in HCV Treatment
4. Therapeutic efficacy of the small molecule GS-5734 against Ebola virus in rhesus monkeys
5. Phosphoramidate ProTides of the Anticancer Agent FUDR Successfully Deliver the Preformed Bioactive Monophosphate in Cells and Confer Advantage over the Parent Nucleoside
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