Literature DB >> 24119090

Effectiveness of novel 5-(5-amino-1-aryl-1H-pyrazol-4-yl)-1H-tetrazole derivatives against promastigotes and amastigotes of Leishmania amazonensis.

Viviane dos Santos Faiões1, Leonor L Leon, Marilene M Canto-Cavalheiro, Eduardo C Torres-Santos, Alice M R Bernardino, Percilene F Vegi, Maurício S dos Santos.   

Abstract

In this research, a series of substituted 5-(5-amino-1-aryl-1H-pyrazol-4-yl)-1H-tetrazoles were synthesized and evaluated for in vitro antileishmanial activity. Among the derivatives, examined compounds 3b and 3l exhibited promising activity against promastigotes and amastigotes forms of Leishmania amazonensis. The cytotoxicity of these compounds was evaluated on murine cells, giving access to the corresponding selectivity index (SI).
© 2013 John Wiley & Sons A/S.

Entities:  

Keywords:  Leishmania amazonensis; antileishmanial activity; tetrazole derivatives

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Year:  2013        PMID: 24119090     DOI: 10.1111/cbdd.12235

Source DB:  PubMed          Journal:  Chem Biol Drug Des        ISSN: 1747-0277            Impact factor:   2.817


  2 in total

1.  The new pyrazolyltetrazole derivative MSN20 is effective via oral delivery against cutaneous leishmaniasis.

Authors:  Viviane Dos Santos Faiões; Maurício Silva Dos Santos; Alice Maria Rolim Bernardino; Edézio Ferreira Cunha-Júnior; Marilene Marcuzzo do Canto Cavalheiro; Eduardo Caio Torres-Santos
Journal:  Antimicrob Agents Chemother       Date:  2014-08-04       Impact factor: 5.191

2.  Synthesis, single crystal analysis, biological and docking evaluation of tetrazole derivatives.

Authors:  Hamid Aziz; Aamer Saeed; Farukh Jabeen; Noor Ud Din; Ulrich Flörke
Journal:  Heliyon       Date:  2018-09-17
  2 in total

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