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 …
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 …
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 …
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) …
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 …
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 …
Background/Objectives: Pteridine reductase 1 (PTR1) has been one of the prime targets for discovering novel antileishmanial therapeutics in the fight against Leishmaniasis. This …
A series of thiazolopyrimidine derivatives was designed and synthesized as a Leishmania major pteridine reductase 1 (LmPTR1) enzyme inhibitor. Their LmPTR1 inhibitor activities …