Journal
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
Volume 59, Issue 10, Pages 6648-6652Publisher
AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.01371-15
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Funding
- Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [2011/50318-1]
- Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) [573530/2008-4]
- Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)
- Pro-Reitoria de Pesquisa da Universidade de Sao Paulo (PRP-USP) [2011.1.9352.1.8]
- Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [11/50318-1] Funding Source: FAPESP
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In recent years, a class of oxindole-copper and -zinc complex derivatives have been reported as compounds with efficient proapoptotic activity toward different tumor cells (e.g., neuroblastomas, melanomas, monocytes). Here we assessed the efficacy of synthesized oxindole-copper(II), -zinc(II), and -vanadyl (VO2+) complexes against adult Schistosoma mansoni worms. The copper( II) complexes (50% inhibitory concentrations of 30 to 45 mu M) demonstrated greater antischistosomal properties than the analogous zinc and vanadyl complexes regarding lethality, reduction of motor activity, and oviposition.
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