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Home / Archives for Marques M

Marques M

In vitro drug susceptibility of Leishmania infantum isolated from humans and dogs

  • Autores: Campino L, Henriques S, Maia C, Marques M, Nunes M, Rolão N
  • Ano de Publicação: 2013
  • Journal: Experimental Parasitology
  • Link: http://www.ncbi.nlm.nih.gov/pubmed/23747751

Visceral leishmaniasis (VL) caused by parasites of Leishmania donovani complex is a severe human disease which often leads to death if left untreated. Domestic dogs are the main reservoir hosts for zoonotic human visceral infection caused by Leishmania infantum. In the absence of effective human and dog vaccines, the only feasible way to treat and control leishmaniasis is through the use of suitable medications.
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Non-classic metallointercalators with dipyridophenazine: DNA interaction studies and leishmanicidal activity

  • Autores: Campino L, de Sousa B, Farrell N, Madureira J, Maia C, Marques M, Ramos CIV, Santana-Marques MG
  • Ano de Publicação: 2013
  • Journal: Inorganic Chemistry
  • Link: http://pubs.acs.org/doi/abs/10.1021/ic401067d

[Cu(II)(dppz)2(AcOO)]+ and [Zn(II)(dppz)2]2+ bind DNA by intercalation and covalent binding modes. A loss of a dppz unit, which occurs only when DNA is present, justifies such dual binding mode.
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Synthesis, structural characterization and leishmanicidal activity evaluation of ferrocenyl N-heterocyclic compounds

  • Autores: Campino L, Helena Garcia M, Madureira J, Maia C, Marques M, Matos CP, Morais TS, Paula Robalo M, Piedade MFM, Quintal S, Villa De Brito MJ
  • Ano de Publicação: 2013
  • Journal: Journal of Organometallic Chemistry
  • Link: http://www.sciencedirect.com/science/article/pii/S0022328X13005512

New ferrocenyl derivatives with the general formula FcC(O)L [Fc = (η5-C5H5)Fe(η5-C5H4)], where L is an aminoquinoline or hydroxyaminoquinoline, have been synthesized for evaluation of their leishmanicidal properties. The compounds were designed with ferrocene coupled to the quinolines by an amide or ester bridge. Ferrocenyl component is intended to act as quinoline carrier and ROS producer after in vivo oxidation to Fe(III), while decreasing normal cell cytotoxicity of coupled quinolines. The bridge was chosen based on its known ability to undergo hydrolysis by the protease/esterase rich media in phagolysosomes, the target of the intracellular form of leishmania parasites.
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