Leishmaniasis is a globally distributed zoonosis and a major challenge to public health, with increasing incidence and limited therapeutic options marked by toxicity and emerging resistance. Aiming to identify safer and more effective alternatives for disease control, this study evaluated the antileishmanial potent...
Fernanda Melo Jucá, Damião Sampaio de Sousa, Caio Henrique Alexandre Roberto et al.· ChemistrySelect· 0 citations
In silico results highlight XN5 as a promising candidate for Chagas disease treatment, showing multi-parameter optimization scores of 5, molecular weights below 400 g/mol, and advantageous absorption and permeability profiles.
Rafael de Oliveira Marinho, Caroline Do Nascimento Gonçalves, Jacilene Silva et al.· Journal of Pharmaceutical In...· 0 citations
Overall, compound 4 highlights the potential of dual-redox quinone platforms to induce ferroptosis, providing a viable lead candidate for novel antineoplastic drug discovery in prostate cancer and other malignancies.
E. N. Mendoza, Maria Fernanda Madrid, P. M. D. da Costa et al.· ACS Omega· 0 citations
Although the evaluated thiadiazine derivatives lacked direct antibacterial activity, they significantly enhanced the efficacy of antibiotics against multidrug-resistant bacteria.
E. D. da Silva, I. G. P. Dantas, Matheus dos Santos Lourenço et al.· Antibiotics· 0 citations
Results suggest that flavonoids, particularly amentoflavone, represent promising scaffolds for the development of antiviral and antioxidant agents against WSSV, warranting further experimental validation.
Damião Sampaio de Sousa, João Miguel Lopes de Melo Lima, Jacilene Silva et al.· Molecular diversity· 0 citations
The results showed that the QNL1 and QNL3 derivatives were the most favorable due to high intestinal absorption and apparent permeability and apparent permeability, showing potential as a future drug.
M. Sales, Caroline Do Nascimento Gonçalves, Abraão Lucas Silva dos Santos et al.· Discover Chemistry· 0 citations
A machine learning-guided quantitative structure-activity relationship (QSAR) workflow was developed to prioritize fluconazole analogs and FDA-approved drugs with predicted antifungal activity against Candida, followed by a structure-based exploration of a cell wall target.
Hamza Age Daudo, E. Marinho, Victor Moreira de Oliveira et al.· Molecular diversity· 0 citations
It is suggested that V. gardneriana EO has moderate antifungal activity, however, it shows promising potential when combined with conventional antifungal agents and supports future research toward the development of therapeutic formulations.
Amanda L. Barros, F. L. L. de Aguiar, Andréa Maria Neves et al.· Anais da Academia Brasileira...· 0 citations
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