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1.
J Inorg Biochem ; 199: 110756, 2019 10.
Article in English | MEDLINE | ID: mdl-31299378

ABSTRACT

Three novel Py2N2-cobalt(III) complexes with the 5-hydroxy-1,4-naphthoquinone nuclei (NQ) were evaluated as potential hypoxia-activated anticancer prodrugs. The complexes were synthesized and fully characterized by IR and UV-Visible spectroscopies, ESI mass spectrometry and CHN elemental analysis. Structural information was obtained from density functional theory (DFT) calculations. Cyclic voltammetry analysis in acetonitrile indicates that the ligand substituents (H, CH3 and p-tolylthio) do not have a relevant effect on the Co3+/Co2+ redox potential. Reactions with ascorbic acid in phosphate buffers were performed to simulate redox activation of the complexes in biological media. Fast and irreversible dissociation of the NQ ligands was observed for all complexes upon Co3+/Co2+ reduction. Cytotoxic activity of complexes 1 and 3 was evaluated in tumor cells (HT-29 and HCT-116) under hypoxic and normoxic conditions.


Subject(s)
Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacology , Cell Hypoxia/physiology , Cobalt/chemistry , Naphthoquinones/chemistry , Ascorbic Acid/chemistry , Cell Survival/drug effects , Coordination Complexes/chemistry , Electrochemistry , HCT116 Cells , HT29 Cells , Humans , Molecular Structure
2.
Eur J Med Chem ; 150: 920-929, 2018 Apr 25.
Article in English | MEDLINE | ID: mdl-29602038

ABSTRACT

Leishmaniasis is a group of infectious neglected tropical diseases caused by more than 20 pathogenic species of Leishmania sp. Due to the limitations of the current treatments available, chalcone moiety has been drawn with a lot of attention due to the simple chemistry and synthesis, being reported with antileishmanial activity in particular against amastigote form. This review aims to provide an overview towards antileishmanial activity of chalcones derivatives against amastigote form for Leishmania major, L. amazonensis, L. panamensis, L. donovani and L. infantum as well as their structure-activity relationship (SAR), molecular targets and in silico ADMET evaluation. In this way, it is expected that this review may support the research and development of new promising chalcones candidates a leishmanicidal drugs.


Subject(s)
Antiprotozoal Agents/pharmacology , Chalcone/pharmacology , Leishmania/drug effects , Antiprotozoal Agents/chemical synthesis , Antiprotozoal Agents/chemistry , Chalcone/chemical synthesis , Chalcone/chemistry , Dose-Response Relationship, Drug , Drug Design , Humans , Molecular Structure , Parasitic Sensitivity Tests , Structure-Activity Relationship
3.
Arch Virol ; 162(6): 1577-1587, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28213871

ABSTRACT

Mayaro virus (MAYV) is an arthropod-borne virus and a member of the family Togaviridae, genus Alphavirus. Its infection leads to an acute illness accompanied by long-lasting arthralgia. To date, there are no antiviral drugs or vaccines against infection with MAYV and resources for the prevention or treatment of other alphaviruses are very limited. MAYV has served as a model to study the antiviral potential of several substances on alphavirus replication. In this work we evaluated the antiviral effect of seven new derivatives of thieno[2,3-b]pyridine against MAYV replication in a mammalian cell line. All derivatives were able to reduce viral production effectively at concentrations that were non-toxic for Vero cells. Molecular modeling assays predicted low toxicity risk and good oral bioavailability of the substances in humans. One of the molecules, selected for further study, demonstrated a strong anti-MAYV effect at early stages of replication, as it protected pre-treated cells and also during the late stages, affecting virus morphogenesis. This study is the first to demonstrate the antiviral effect of thienopyridine derivatives on MAYV replication in vitro, suggesting the potential application of these substances as antiviral molecules against alphaviruses. Additional in vivo research will be needed to expand the putative therapeutic applications.


Subject(s)
Alphavirus/drug effects , Antiviral Agents/chemistry , Antiviral Agents/pharmacology , Pyridines/pharmacology , Thiophenes/pharmacology , Animals , Chlorocebus aethiops , Humans , Pyridines/chemical synthesis , Pyridines/chemistry , Pyridines/toxicity , Thiophenes/chemical synthesis , Thiophenes/chemistry , Thiophenes/toxicity , Vero Cells , Virus Replication/drug effects
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