Publications by authors named "Renata Priscila Barros de Menezes"

Toxoplasma gondii, an obligate intracellular parasite, infects approximately one-third of the global population, making toxoplasmosis a significant public health concern. The current treatment - typically a combination of pyrimethamine and sulfadiazine - is limited to the acute phase of infection, and it often causes allergic reactions and severe side effects. Marinoquinolines (MQs), a class of compounds originally isolated from marine microorganisms, have exhibited promising pharmacological properties including anti-T.

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Neglected tropical diseases such as Leishmaniasis and Chagas disease remain critical public health challenges. This study applied ligand-based virtual screening to a dataset of 4,150 secondary metabolites from the Lamiaceae family, aiming to identify multitarget molecules against four Leishmania species (L. infantum, L.

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Leishmaniasis is a neglected tropical disease caused by a protozoan of the genus Leishmania, which has visceral and cutaneous forms. The symptoms of leishmaniasis include high fever and weakness, and the cutaneous infection also causes lesions under the skin. The drugs used to treat leishmaniasis have become less effective due to the resistance mechanisms of the protozoa.

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The COVID-19 pandemic has caused over 7 million deaths globally in the past four years. spp. (Siparunaceae), which is used in Brazilian folk medicine, is considered a genus with potential antiviral alternatives.

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Leishmaniasis, caused by Leishmania parasites, presents a major global health challenge due to limitations of existing treatments, including toxicity, side effects, drug resistance, and high costs. This study utilized the MuDRA (Multi-Descriptor Read Across) model for virtual screening to identify potential anti-Leishmania infantum compounds. A set of 15 terpenes and steroids was screened, leading to the identification of four promising candidates-lupeol, xylodiol, morolic acid, and trachyloban-18-oic acid.

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Article Synopsis
  • Chagas disease and leishmaniasis are widespread in Latin America, and current treatments are insufficient, making natural products, particularly from the Amaryllidaceae family, promising for developing new therapies due to their antiparasitic alkaloids.
  • The study aimed to test the anti-parasitic effects of five natural isoquinoline alkaloids isolated from Hippeastrum aulicum against different stages of Trypanosoma cruzi and Leishmania infantum, using both in silico and in vitro methods, as well as molecular docking techniques.
  • Results indicated that haemanthamine and lycorine were the most effective against both parasites, with additional promising activity shown by 7-methoxy-O-m
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Article Synopsis
  • * Marinoquinolines, derived from marine bacteria, show promising in vitro anti-toxoplasmosis activity with effective concentration values between 1.31 and 3.78 µM.
  • * One specific compound, MQ-1, demonstrated significant reductions in parasite levels in infected mice, highlighting its potential as a new therapeutic option for treating toxoplasmosis. *
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  • Thrombosis is a serious health issue linked to various vascular diseases, and research has identified phenolic compounds (PCs) in medicinal plants that may help inhibit blood coagulation and platelet aggregation.
  • This study focused on surveying natural PCs with antithrombotic and antiplatelet properties, while also evaluating their physical and toxicological characteristics using drug-likeness criteria.
  • The findings revealed 246 PCs with potential benefits, 125 of which showed non-toxicity and adhered to important pharmaceutical guidelines, highlighting their promise as new candidates for preventing cardiovascular issues.
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Major depressive disorder is a severe mood disorder characterized by different emotions and feelings. This study investigated the antidepressant activity of the phenylpropanoid methyleugenol (ME) in adult female mice exposed to a stress model induced by dexamethasone. The animals were randomly divided into groups containing eight animals and were pre-administered with dexamethasone (64 μg/kg subcutaneously).

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Toxoplasmosis is a significant public health concern with limited therapeutic options. The medicines for malaria venture (MMV) developed the pandemic response box (PRB) containing 400 drug-like molecules with broad pathogen activity. The aim of this work is to evaluate PRB compounds for their anti- activity and identify promising candidates for further evaluation.

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This study analysed the phytochemical profile of extract and the molecular interactions of its main compounds with TRPV1 and CB2, target receptors in the Burning Mouth Syndrome (BMS) pathogenesis. The phytochemical profile of s floral buds extract treated with activated charcoal (TCEE) was analysed by High-Performance Liquid Chromatography (HPLC) coupled to Mass Spectrometry (LC-MS). The quantification of spilanthol was analysed by HPLC coupled to a Diode-Array Detector (HPLC-DAD).

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Toxoplasmosis, caused by the obligate intracellular parasite Toxoplasma gondii, affects about one-third of the world's population and can cause severe congenital, neurological and ocular issues. Current treatment options are limited, and there are no human vaccines available to prevent transmission. Drug repurposing has been effective in identifying anti-T.

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The bifunctional enzyme Dihydrofolate reductase-thymidylate synthase (DHFR-TS) plays a crucial role in the survival of the parasite, as folates are essential cofactors for purine and pyrimidine nucleotide biosynthesis. However, DHFR inhibitors are largely ineffective in controlling trypanosomatid infections, largely due to the presence of Pteridine reductase 1 (PTR1). Therefore, the search for structures with dual inhibitory activity against PTR1/DHFR-TS is crucial in the development of new anti- chemotherapies.

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Introduction: Alzheimer's disease (AD) is the most studied progressive eurodegenerative disorder, affecting 40-50 million of the global population. This progressive neurodegenerative disease is marked by gradual and irreversible declines in cognitive functions. The unavailability of therapeutic drug candidates restricting/reversing the progression of this dementia has severed the existing challenge.

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The World Health Organization classifies Leishmania as one of the 17 “neglected diseases” that burden tropical and sub-tropical climate regions with over half a million diagnosed cases each year. Despite this, currently available anti-leishmania drugs have high toxicity and the potential to be made obsolete by parasite drug resistance. We chose to analyze organoselenides for leishmanicidal potential given the reduced toxicity inherent to selenium and the displayed biological activity of organoselenides against Leishmania.

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Eriocaulaceae is a pantropical family whose main center of biodiversity is in Brazil. In general, the family has about 1200 species, in which phytochemical and biological studies have shown a variety of structures and activities. The aim of this research is to compile the compounds isolated in the Eriocaulaceae family and carry out a computational study on their biological targets.

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Here we report the development of MolPredictX, an innovate and freely accessible web interface for biological activity predictions of query molecules. MolPredictX utilizes in-house QSAR models to provide 27 qualitative predictions (active or inactive), and quantitative probabilities for bioactivity against parasitic (Trypanosoma and Leishmania), viral (Dengue, Sars-CoV and Hepatitis C), pathogenic yeast (Candida albicans), bacterial (Salmonella enterica and Escherichia coli), and Alzheimer disease enzymes. In this article, we introduce the methodology and usability of this webtool, highlighting its potential role in the development of new drugs against a variety of diseases.

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Article Synopsis
  • The study focuses on plants from the Hyptidinae subtribe in the Lamiaceae family, known for producing bioactive molecules that could be potential drug candidates.* -
  • Researchers isolated and chemically characterized four diterpenes (Pomiferin D, Salviol, Pomiferin E, and 2α-hydroxysugiol) along with two phenolic compounds (rosmarinic and caffeic acids) using NMR techniques.* -
  • The biological activity of the isolated compounds was tested, resulting in certain minimal inhibitory concentrations (MIC), with varying levels of effectiveness against specific targets, but some compounds showed no significant activity at the tested concentrations.*
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Schistosomiasis is a chronic parasitic disease caused by trematodes of the genus ; it is commonly caused by , which is transmitted by snails. Studies show that more than 200 million people are infected and that more than 90% of them live in Africa. Treatment with praziquantel has the best cost-benefit result on the market.

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  • * The study aimed to identify natural products from the Annonaceae family that could work as antichagasic agents and successfully screened 57 molecules, later testing 16 of them in the lab.
  • * Out of the tested molecules, six showed new antiepimastigote activity, with 13-epicupressic acid emerging as the most promising candidate due to its effectiveness against the amastigote form of T. cruzi.
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Essential oils (EOs) are a mixture of chemical compounds with a long history of use in food, cosmetics, perfumes, agricultural and pharmaceuticals industries. The main object of this study was to find chemical patterns between 45 EOs and antiprotozoal activity (antiplasmodial, antileishmanial and antitrypanosomal), using different machine learning algorithms. In the analyses, 45 samples of EOs were included, using unsupervised Self-Organizing Maps (SOM) and supervised Random Forest (RF) methodologies.

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Article Synopsis
  • Natural products, including plant extracts and essential oils, show potential as anti-SARS-CoV agents, which could lead to new drug development against coronaviruses.
  • The study reviewed recent research on medicinal plants and identified 29 species and over 300 compounds, with flavonoids and terpenes emerging as promising candidates.
  • Emphasizing the importance of ethnopharmacology, the paper advocates for combined in silico and in vitro methods to enhance antiviral research and discovery.
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Background: The emergence of a new coronavirus (CoV), named 2019-nCoV, as an outbreak originated in the city of Wuhan, China, has resulted in the death of more than 3,400 people this year alone and has caused worldwide an alarming situation, particularly following previous CoV epidemics, including the Severe Acute Respiratory Syndrome (SARS) in 2003 and the Middle East Respiratory Syndrome (MERS) in 2012. Currently, no exists for infections caused by CoVs; however, some natural products may represent potential treatment resources, such as those that contain diterpenes.

Objective: This study aimed to use computational methods to perform a virtual screening (VS) of candidate diterpenes with the potential to act as CoV inhibitors.

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