Evaluation of the antiprotozoan properties of 5′-norcarbocyclic pyrimidine nucleosides

KJ Alzahrani, ES Matyugina… - Bioorganic & medicinal …, 2017 - Elsevier
Carbocyclic nucleoside analogues have a distinguished history as anti-infectious agents,
including key antiviral agents. Toxicity was initially a concern but this was reduced by the …

Investigation of 5'-norcarbocyclic nucleoside analogues as antiprotozoal and antibacterial agents

AL Khandazhinskaya, ES Matyugina, PN Solyev… - Molecules, 2019 - mdpi.com
Carbocyclic nucleosides have long played a role in antiviral, antiparasitic, and antibacterial
therapies. Recent results from our laboratories from two structurally related scaffolds have …

N6-modification of 7-deazapurine nucleoside analogues as anti-Trypanosoma cruzi and anti-Leishmania agents: Structure-activity relationship exploration and in vivo …

C Lin, DGJ Batista, AL Mazzeti, RD Girao… - European Journal of …, 2022 - Elsevier
Chagas disease and leishmaniasis are two poverty-related neglected tropical diseases that
cause high mortality and morbidity. Current treatments suffer from severe limitations and …

Revisiting Pyrazolo[3,4-d]pyrimidine Nucleosides as Anti-Trypanosoma cruzi and Antileishmanial Agents

J Bouton, L Ferreira de Almeida Fiuza… - Journal of Medicinal …, 2021 - ACS Publications
Chagas disease and visceral leishmaniasis are two neglected tropical diseases responsible
for numerous deaths around the world. For both, current treatments are largely inadequate …

Antitrypanosomal activity of purine nucleosides can be enhanced by their conversion to O-acetylated derivatives

JR Sufrin, D Rattendi, AJ Spiess, S Lane… - Antimicrobial agents …, 1996 - Am Soc Microbiol
Fifteen purine nucleosides and their O-acetylated ester derivatives were examined for in
vitro antitrypanosomal activity against the LAB 110 EATRO isolate of Trypanosoma brucei …

Structurally diverse 5-substituted pyrimidine nucleosides as inhibitors of Leishmania donovani promastigotes in vitro

PF Torrence, X Fan, X Zhang, PM Loiseau - Bioorganic & medicinal …, 2006 - Elsevier
The following structurally diverse 5-substituted-2′-deoxyuridine nucleosides displayed
potent in vitro antileishmanial activity: 5-formyl, 5-(2, 2,-dicyanovinyl)-, 5-(2-cyano-2 …

Synthesis and in vitro antileishmanial activity of 5-substituted-2′-deoxyuridine derivatives

C Peyron, R Benhida, C Bories, PM Loiseau - Bioorganic chemistry, 2005 - Elsevier
We report herein the synthesis and the in vitro antileishmanial evaluation of 5-substituted-
2′-deoxyuridine nucleosides. The most active compound against Leishmania donovani …

Discovery of Novel 7-Aryl 7-Deazapurine 3′-Deoxy-ribofuranosyl Nucleosides with Potent Activity against Trypanosoma cruzi

F Hulpia, K Van Hecke, C França da Silva… - Journal of Medicinal …, 2018 - ACS Publications
Chagas disease is the leading cause of cardiac-related mortality in Latin American countries
where it is endemic. Trypanosoma cruzi, the disease-causing pathogen, is unable to …

6‐Methyl‐7‐Aryl‐7‐Deazapurine Nucleosides as Anti‐Trypanosoma cruzi Agents: Structure‐Activity Relationship and in vivo Efficacy

C Lin, L Ferreira de Almeida Fiuza… - …, 2021 - Wiley Online Library
Chagas disease is a tropical infectious disease resulting in progressive organ‐damage and
currently lacks efficient treatment and vaccine options. The causative pathogen …

Structure–Activity Relationship Exploration of 3′-Deoxy-7-deazapurine Nucleoside Analogues as Anti-Trypanosoma brucei Agents

F Hulpia, GD Campagnaro, KJ Alzahrani… - ACS Infectious …, 2020 - ACS Publications
Human African trypanosomiasis is a neglected tropical disease caused by Trypanosoma
brucei parasites. These protists are unable to produce the purine ring, making them …