Synthesis and evaluation of novel prenylated chalcone derivatives as anti-leishmanial and anti-trypanosomal compounds

TG Passalacqua, LA Dutra, L De Almeida… - Bioorganic & Medicinal …, 2015 - Elsevier
Chalcones form a class of compounds that belong to the flavonoid family and are widely
distributed in plants. Their simple structure and the ease of preparation make chalcones …

Total synthesis of the natural chalcone lophirone E, synthetic studies toward benzofuran and indole-based analogues, and investigation of anti-leishmanial activity

L Pozzetti, R Ibba, S Rossi, O Taglialatela-Scafati… - Molecules, 2022 - mdpi.com
The potential of natural and synthetic chalcones as therapeutic leads against different
pathological conditions has been investigated for several years, and this class of …

Novel prenyloxy chalcones as potential leishmanicidal and trypanocidal agents: design, synthesis and evaluation

JC Espinoza-Hicks, KF Chacón-Vargas… - European Journal of …, 2019 - Elsevier
The available drugs for treating Leishmaniasis and American trypanosomiasis have high
toxicity and multiple side effects, among other problems. More effective and less toxic …

Methoxylated 2'-hydroxychalcones as antiparasitic hit compounds

C Borsari, N Santarem, J Torrado, AI Olías… - European Journal of …, 2017 - Elsevier
Chalcones display a broad spectrum of pharmacological activities. Herein, a series of 2'-
hydroxy methoxylated chalcones was synthesized and evaluated towards Trypanosoma …

Identification of chalcone-based antileishmanial agents targeting trypanothione reductase

M Ortalli, A Ilari, G Colotti, I De Ionna, T Battista… - European journal of …, 2018 - Elsevier
All currently used first-line and second-line drugs for the treatment of leishmaniasis exhibit
several drawbacks including toxicity, high costs and route of administration. Furthermore …

Trypanocidal and leishmanicidal properties of substitution-containing chalcones

F Lunardi, M Guzela, AT Rodrigues… - Antimicrobial Agents …, 2003 - Am Soc Microbiol
Ten chalcones were synthesized and tested as potential leishmanicidal and trypanocidal
agents. All tested compounds caused concentration-dependent inhibition of the in vitro …

Synthesis, Cytotoxicity, and Anti-Trypanosoma cruzi Activity of New Chalcones

JC Aponte, M Verástegui, E Málaga… - Journal of Medicinal …, 2008 - ACS Publications
Synthesis of a cytotoxic dihydrochalcone, first isolated from a traditional Amazonian
medicinal plant Iryanthera juruensis Warb (Myristicaceae), followed by a comprehensive …

Synthesis, biological evaluation and SAR of sulfonamide 4-methoxychalcone derivatives with potential antileishmanial activity

CR Andrighetti-Fröhner, KN de Oliveira… - European Journal of …, 2009 - Elsevier
Despite clinical importance of leishmaniasis, an infectious disease that affects 12 thousand
million people in 88 countries, the treatment is still unsatisfactory due to its limited efficacy …

The chemotherapeutic potential of chalcones against leishmaniases: a review

N Tajuddeen, MB Isah, MA Suleiman… - International journal of …, 2018 - Elsevier
Leishmaniases are endemic diseases in tropical and sub-tropical regions of the world and
are considered by the World Health Organization (WHO) to be among the six most important …

Synthesis, structure and in vitro anti-trypanosomal activity of non-toxic arylpyrrole-based chalcone derivatives

AI Zulu, OO Oderinlo, C Kruger, M Isaacs, HC Hoppe… - Molecules, 2020 - mdpi.com
With an intention of identifying chalcone derivatives exhibiting anti-protozoal activity, a
cohort of relatively unexplored arylpyrrole-based chalcone derivatives were synthesized in …