Cargando…
Acyclic nucleoside phosphonates with adenine nucleobase inhibit Trypanosoma brucei adenine phosphoribosyltransferase in vitro
All medically important unicellular protozoans cannot synthesize purines de novo and they entirely rely on the purine salvage pathway (PSP) for their nucleotide generation. Therefore, purine derivatives have been considered as a promising source of anti-parasitic compounds since they can act as inhi...
Autores principales: | Doleželová, Eva, Klejch, Tomáš, Špaček, Petr, Slapničková, Martina, Guddat, Luke, Hocková, Dana, Zíková, Alena |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233378/ https://www.ncbi.nlm.nih.gov/pubmed/34172767 http://dx.doi.org/10.1038/s41598-021-91747-6 |
Ejemplares similares
-
Acyclic nucleoside phosphonates containing a second phosphonate group are potent inhibitors of the 6-oxopurine phosphoribosyltransferases and have antimalarial activity
por: Keough, Dianne, et al.
Publicado: (2014) -
Trypanosoma brucei adenine-phosphoribosyltransferases mediate adenine salvage and aminopurinol susceptibility but not adenine toxicity()
por: Lüscher, Alexandra, et al.
Publicado: (2013) -
Crystal structures and inhibition of Trypanosoma brucei hypoxanthine–guanine phosphoribosyltransferase
por: Terán, David, et al.
Publicado: (2016) -
Evaluation of the Trypanosoma brucei 6-oxopurine salvage pathway as a potential target for drug discovery
por: Doleželová, Eva, et al.
Publicado: (2018) -
Characterization of adenine phosphoribosyltransferase (APRT) activity in Trypanosoma brucei brucei: Only one of the two isoforms is kinetically active
por: Glockzin, Kayla, et al.
Publicado: (2022)