Chalcone derivatives: promising starting points for drug design

MN Gomes, EN Muratov, M Pereira, JC Peixoto… - Molecules, 2017 - mdpi.com
Medicinal chemists continue to be fascinated by chalcone derivatives because of their
simple chemistry, ease of hydrogen atom manipulation, straightforward synthesis, and a …

Structure based medicinal chemistry-driven strategy to design substituted dihydropyrimidines as potential antileishmanial agents

U Rashid, R Sultana, N Shaheen, SF Hassan… - European journal of …, 2016 - Elsevier
In an attempt to explore novel and more potent antileishmanial compounds to diversify the
current inhibitors, we pursued a medicinal chemistry-driven strategy to synthesize novel …

Targeting pteridine reductase 1 and dihydrofolate reductase: the old is a new trend for leishmaniasis drug discovery

GM das Neves, LP Kagami, IL Gonçalves… - Future Medicinal …, 2019 - Taylor & Francis
Leishmaniasis is one of the major neglected tropical diseases in the world and it is
considered endemic in 88 countries. This disease is transmitted by a Leishmania spp …

Exploring actinomycetes natural products to identify potential multi-target inhibitors against Leishmania donovani

S Singh, VK Prajapati - 3 Biotech, 2022 - Springer
Visceral leishmaniasis (VL) is a neglected tropical disease that mainly affects the poor
population of the Indian, African, and South American subcontinent. The increasing …

Ionic liquid-assisted synthesis of dihydropyrimidin (thi) one Biginelli adducts and investigation of their mechanism of urease inhibition

TC Braga, TF Silva, TMS Maciel, ECD da Silva… - New Journal of …, 2019 - pubs.rsc.org
Twenty-six Biginelli adducts were synthesized through an ionic liquid-assisted synthesis
with up to 92% yield. Sixteen of these Biginelli adducts were then assayed to determine their …

Cynaroside inhibits Leishmania donovani UDP-galactopyranose mutase and induces reactive oxygen species to exert antileishmanial response

S Tabrez, F Rahman, R Ali, AS Alouffi… - Bioscience …, 2021 - portlandpress.com
Cynaroside, a flavonoid, has been shown to have antibacterial, antifungal and anticancer
activities. Here, we evaluated its antileishmanial properties and its mechanism of action …

Challenging the Biginelli scaffold to surpass the first line antitubercular drugs: Mycobacterium tuberculosis thymidine monophosphate kinase (TMPKmt) inhibition …

MS El-Shoukrofy, A Atta, S Fahmy… - Journal of Enzyme …, 2024 - Taylor & Francis
New Biginelli adducts were rationalised, via the introduction of selected anti-tubercular (TB)
pharmacophores into the dihydropyrimidine (DHPM) ring of deoxythymidine …

Chitosan-based macrophage-mediated drug targeting for the treatment of experimental visceral leishmaniasis

S Kunjachan, S Gupta, AK Dwivedi… - Journal of …, 2011 - Taylor & Francis
The potential of chitosan microparticles as a carrier of doxorubicin for the treatment of
visceral leishmaniasis was evaluated by macrophage-mediated drug targeting approach …

[HTML][HTML] Preliminary Information of Iranian Lizard Leishmania Promastigote Transcriptome Sequencing by Next Generation Sequencing (NGS) Method

F Ehya, S Kalantari, M Bandehpour… - Iranian Journal of …, 2023 - ncbi.nlm.nih.gov
Background: A lizard Leishmania has been isolated from a lizard (Agama agilis) in Iran. Its
genome sequence has not been determined, so far. Methods: The study was done at Shahid …

Leishmanicidal Potential of Hardwickiic Acid Isolated From Croton sylvaticus

JA Crentsil, LRT Yamthe, BZ Anibea, E Broni… - Frontiers in …, 2020 - frontiersin.org
Leishmania is a parasitic protozoon responsible for the neglected tropical disease
Leishmaniasis. Approximately, 350 million people are susceptible and close to 70,000 death …