(FFN) Ciencias Farmacéuticas
Departamento académico
Universidade Federal do Rio de Janeiro
Río de Janeiro, BrasilPublicaciones en colaboración con investigadores/as de Universidade Federal do Rio de Janeiro (10)
2019
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A step towards development of promising trypanocidal agents: Synthesis, characterization and in vitro biological evaluation of ferrocenyl Mannich base-type derivatives
European Journal of Medicinal Chemistry, Vol. 163, pp. 569-582
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Antichagasic profile of a Series of Mannich Base-Type Derivatives: Design, Synthesis, in vitro Evaluation, and Computational Studies Involving Iron Superoxide Dismutase
ChemistrySelect, Vol. 4, Núm. 27, pp. 8112-8121
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Rational modification of Mannich base-type derivatives as novel antichagasic compounds: Synthesis, in vitro and in vivo evaluation
Bioorganic and Medicinal Chemistry, Vol. 27, Núm. 17, pp. 3902-3917
2018
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Second Generation of Mannich Base-Type Derivatives with in Vivo Activity against Trypanosoma cruzi
Journal of Medicinal Chemistry, Vol. 61, Núm. 13, pp. 5643-5663
2016
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In Vitro and in Vivo Anti-Trypanosoma cruzi Activity of New Arylamine Mannich Base-Type Derivatives
Journal of Medicinal Chemistry, Vol. 59, Núm. 24, pp. 10929-10945
2009
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Selective activity against Mycobacterium tuberculosis of new quinoxaline 1,4-di-N-oxides
Bioorganic and Medicinal Chemistry, Vol. 17, Núm. 1, pp. 385-389
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Synthesis, trypanocidal activity and docking studies of novel quinoxaline-N-acylhydrazones, designed as cruzain inhibitors candidates
Bioorganic and Medicinal Chemistry, Vol. 17, Núm. 2, pp. 641-652
2008
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Antiplasmodial structure-activity relationship of 3-trifluoromethyl-2-arylcarbonylquinoxaline 1,4-di-N-oxide derivatives
Experimental Parasitology, Vol. 118, Núm. 1, pp. 25-31
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Unexpected reduction of ethyl 3-phenylquinoxaline-2-carboxylate 1,4-Di-N-oxide derivatives by amines
Molecules
2005
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Comparative use of solvent-free KF-Al2O3 and K 2CO3 in acetone in the synthesis of quinoxaline 1,4-dioxide derivatives designed as antimalarial drug candidates
Journal of Heterocyclic Chemistry, Vol. 42, Núm. 7, pp. 1381-1385