Universidade Federal do Rio de Janeiro -ko ikertzaileekin lankidetzan egindako argitalpenak (10)

2019

  1. 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

  2. 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

  3. 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

  1. 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

  1. 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

  1. Selective activity against Mycobacterium tuberculosis of new quinoxaline 1,4-di-N-oxides

    Bioorganic and Medicinal Chemistry, Vol. 17, Núm. 1, pp. 385-389

  2. 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

  1. Antiplasmodial structure-activity relationship of 3-trifluoromethyl-2-arylcarbonylquinoxaline 1,4-di-N-oxide derivatives

    Experimental Parasitology, Vol. 118, Núm. 1, pp. 25-31

  2. Unexpected reduction of ethyl 3-phenylquinoxaline-2-carboxylate 1,4-Di-N-oxide derivatives by amines

    Molecules

2005

  1. 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