The potential of secondary metabolites from plants as drugs or leads against protozoan neglected diseases—Part III: In-silico molecular docking investigations

IV Ogungbe, WN Setzer - Molecules, 2016 - mdpi.com
Malaria, leishmaniasis, Chagas disease, and human African trypanosomiasis continue to
cause considerable suffering and death in developing countries. Current treatment options …

Recent advances in the development of broad-spectrum antiprotozoal agents

A Moreno-Herrera, S Cortez-Maya… - Current Medicinal …, 2021 - ingentaconnect.com
Infections caused by Trypanosoma brucei, Trypanosoma cruzi, Leishmania spp.,
Entamoeba histolytica, Giardia lamblia, Plasmodium spp., and Trichomonas vaginalis, are …

Discovery of potent pteridine reductase inhibitors to guide antiparasite drug development

A Cavazzuti, G Paglietti, WN Hunter… - Proceedings of the …, 2008 - National Acad Sciences
Pteridine reductase (PTR1) is essential for salvage of pterins by parasitic trypanosomatids
and is a target for the development of improved therapies. To identify inhibitors of …

Antileishmanial phytochemical phenolics: molecular docking to potential protein targets

IV Ogungbe, WR Erwin, WN Setzer - Journal of Molecular Graphics and …, 2014 - Elsevier
A molecular docking analysis has been carried out to examine potential Leishmania protein
targets of antiprotozoal plant-derived polyphenolic compounds. A total of 352 phenolic …

Design, synthesis and biological evaluation of quinazoline derivatives as anti-trypanosomatid and anti-plasmodial agents

C Mendoza-Martínez, J Correa-Basurto… - European journal of …, 2015 - Elsevier
In this paper, the design, synthesis and biological evaluation of a set of quinazoline-2, 4, 6-
triamine derivatives (1–9) as trypanocidal, antileishmanial and antiplasmodial agents are …

Virtual screening identification of nonfolate compounds, including a CNS drug, as antiparasitic agents inhibiting pteridine reductase

S Ferrari, F Morandi, D Motiejunas… - Journal of medicinal …, 2011 - ACS Publications
Folate analogue inhibitors of Leishmania major pteridine reductase (PTR1) are potential
antiparasitic drug candidates for combined therapy with dihydrofolate reductase (DHFR) …

In-silico Leishmania Target Selectivity of Antiparasitic Terpenoids

IV Ogungbe, WN Setzer - Molecules, 2013 - mdpi.com
Neglected Tropical Diseases (NTDs), like leishmaniasis, are major causes of mortality in
resource-limited countries. The mortality associated with these diseases is largely due to …

Computational studies on potential small molecule inhibitors of Leishmania pteridine reductase 1

A Boakye, EN Gasu, JO Mensah… - Journal of Biomolecular …, 2023 - Taylor & Francis
Leishmaniasis is a neglected tropical disease of major public health concern. Challenges
with current therapeutics have led to the exploration of plant medicine for potential …

[HTML][HTML] Natural Product Identification and Molecular Docking Studies of Leishmania Major Pteridine Reductase Inhibitors

MN Arthur, G Hanson, E Broni, PO Sakyi… - Pharmaceuticals, 2024 - mdpi.com
Background/Objectives: Pteridine reductase 1 (PTR1) has been one of the prime targets for
discovering novel antileishmanial therapeutics in the fight against Leishmaniasis. This …

Design, synthesis, and in vitro biological evaluation of novel thiazolopyrimidine derivatives as antileishmanial compounds

H Istanbullu, G Bayraktar, H Akbaba… - Archiv der …, 2020 - Wiley Online Library
A series of thiazolopyrimidine derivatives was designed and synthesized as a Leishmania
major pteridine reductase 1 (LmPTR1) enzyme inhibitor. Their LmPTR1 inhibitor activities …