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Synthesis, biological evaluation and mechanism of action of benzothiazole derivatives with aromatic hydrazone moiety, a new class of antileishmanial compounds.
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- Chemical Biology & Drug Design, 2024, v. 104, n. 1, p. 1, doi. 10.1111/cbdd.14585
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- Article
4-Aminoquinoline Derivatives as Potential Antileishmanial Agents.
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- Chemical Biology & Drug Design, 2015, v. 86, n. 4, p. 704, doi. 10.1111/cbdd.12540
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- Article
7-Chloro-4-quinolinyl Hydrazones: A Promising and Potent Class of Antileishmanial Compounds.
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- Chemical Biology & Drug Design, 2013, v. 81, n. 5, p. 658, doi. 10.1111/cbdd.12112
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- Article
Digitoxigenin presents an effective and selective antileishmanial action against Leishmania infantum and is a potential therapeutic agent for visceral leishmaniasis.
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- Parasitology Research, 2021, v. 120, n. 1, p. 321, doi. 10.1007/s00436-020-06971-2
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- Article
Synthesis, Biological Activity, and Mechanism of Action of 2‐Pyrazyl and Pyridylhydrazone Derivatives, New Classes of Antileishmanial Agents.
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- ChemMedChem, 2018, v. 13, n. 14, p. 1387, doi. 10.1002/cmdc.201800328
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- Article
Synthesis, characterization, and NMR studies of 1,2,3-triazolium ionic liquids: a good perspective regarding cytotoxicity.
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- Journal of Molecular Modeling, 2018, v. 24, n. 7, p. 1, doi. 10.1007/s00894-018-3682-z
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- Article
Parasitological and immunological evaluation of a novel chemotherapeutic agent against visceral leishmaniasis.
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- Parasite Immunology, 2020, v. 42, n. 12, p. 1, doi. 10.1111/pim.12784
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- Article
Antileishmanial compounds from Connarus suberosus: Metabolomics, isolation and mechanism of action.
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- PLoS ONE, 2020, v. 15, n. 11, p. 1, doi. 10.1371/journal.pone.0241855
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- Article
Acarbose presents in vitro and in vivo antileishmanial activity against Leishmania infantum and is a promising therapeutic candidate against visceral leishmaniasis.
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- Medical Microbiology & Immunology, 2021, v. 210, n. 2/3, p. 133, doi. 10.1007/s00430-021-00707-4
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- Article