Publication
Title
6-Methyl-7-deazapurine nucleoside analogues as broad-spectrum antikinetoplastid agents
Author
Abstract
Kinetoplastid parasites are the causative agents of Chagas disease (CD), leishmaniasis and human African trypanosomiasis (HAT). Despite a sustained decrease in the number of HAT cases, more efforts are needed to discover safe and effective therapies against CD and leishmaniasis. Kinetoplastid parasites lack the capability to biosynthesize purines de novo and thus critically depend on uptake and processing of purines from host cells. As such, modified purine nucleoside analogues may act as broad-spectrum antikinetoplastid agents. This study assessed the in vitro activity profile of 7-modified 6-methyl tubercidin derivatives against Trypanosoma cruzi, Leishmania infantum, Trypanosoma brucei brucei and T. b. rhodesiense, and led to the identification of analogues that display activity against all these species, such as 7-ethyl (13) and 7-chloro (7) analogues. These selected analogues also proved sufficiently stable in liver microsomes to warrant in vivo follow-up evaluation.
Language
English
Source (journal)
International Journal for Parasitology: Drugs and Drug Resistance
Publication
2021
ISSN
2211-3207
DOI
10.1016/J.IJPDDR.2021.08.001
Volume/pages
17 (2021) , p. 57-66
ISI
000697478600008
Pubmed ID
34375904
Full text (Publisher's DOI)
Full text (open access)
UAntwerpen
Faculty/Department
Research group
Project info
Modified 7-deazapurine nucleoside analogues for the treatment of human African trypanosomiasis: towards a strong proof-of-concept.
Infla-Med: Fundamental and translational research into targets for the treatment of inflammatory diseases.
Control of sleeping sickness and leishmaniasis: from an insect bite to effective treatment.
Publication type
Subject
Affiliation
Publications with a UAntwerp address
External links
Web of Science
Record
Identifier
Creation 05.10.2021
Last edited 02.10.2024
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