Antiviral Activity of Pd(II) Complexes with Aminoadamantanes Against Arboviruses

Abstract In this paper, we report the synthesis, structural characterization, and antiviral properties of palladium(II) complexes with amantadine (atd) and memantine (mtn). Elemental and mass spectrometric analyses indicated a 1:2 metal/ligand ratio. The single crystal data for Pd‐mtn revealed that the complex adopts a square geometry with the two memantine ligands bonded to Pd(II) by the nitrogen atoms of the NH 2 group, in a trans configuration. Computational studies supported a similar structure for Pd‐atd. The complexes were stable in DMSO solution for 24 h. The antiviral properties of Pd‐atd and Pd‐mtn were evaluated against Zika (ZIKV) and Chikungunya (CHIKV) viruses in vitro at their highest noncytotoxic concentrations. The Pd‐atd (at 2 µM) and Pd‐mtn (at 10 µM) complexes were able to impair 76% and 96% of CHIKV replication, respectively, which points the coordination of amantadine and memantine to Pd(II) as a successful strategy to increase their anti‐CHIKV properties. Conversely, the Pd(II) complexes did not significantly inhibit the replication of ZIKV, which confirms the selectivity towards CHIKV. Interaction of the compounds with N ‐acetyl‐ l ‐cysteine, a model disulfide‐containing peptide, and plasmid DNA pointed to Cys‐containing peptides as more likely targets than nucleotides for the complexes.

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Publication Details

Journal
ChemistrySelect
Published
2024-09-27
DOI
https://doi.org/10.1002/slct.202404225
Citations
1
Primary Topic
HIV/AIDS drug development and treatment
Type
article
Field-Weighted Citation Impact
0.39

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article

Antiviral Activity of Pd(II) Complexes with Aminoadamantanes Against Arboviruses

Anna Karla dos Santos Pereira, Uriel Enrique Aquino Ruiz, Déborah de Alencar Simoni, Douglas Henrique Pereira et al.
1 citations
ChemistrySelect
HIV/AIDS drug development and treatment
0.39
article

Antiviral Activity of Pd(II) Complexes with Aminoadamantanes Against Arboviruses

Anna Karla dos Santos Pereira, Uriel Enrique Aquino Ruiz, Déborah de Alencar Simoni, Douglas Henrique Pereira, Luisa Ronga, Natasha Marques Cassani, Ioannis Kanavos, Állefe Barbosa Cruz, Douglas Hideki Nakahata, Igor Andrade Santos, Pedro P. Corbi, Ana Carolina Gomes Jardim, Ryszard Łobiński, Raphael Enoque Ferraz de Paiva, Daniel Oliveira Silva Martins, Laura Barros Silva
article en
1 citations

Abstract

Abstract In this paper, we report the synthesis, structural characterization, and antiviral properties of palladium(II) complexes with amantadine (atd) and memantine (mtn). Elemental and mass spectrometric analyses indicated a 1:2 metal/ligand ratio. The single crystal data for Pd‐mtn revealed that the complex adopts a square geometry with the two memantine ligands bonded to Pd(II) by the nitrogen atoms of the NH 2 group, in a trans configuration. Computational studies supported a similar structure for Pd‐atd. The complexes were stable in DMSO solution for 24 h. The antiviral properties of Pd‐atd and Pd‐mtn were evaluated against Zika (ZIKV) and Chikungunya (CHIKV) viruses in vitro at their highest noncytotoxic concentrations. The Pd‐atd (at 2 µM) and Pd‐mtn (at 10 µM) complexes were able to impair 76% and 96% of CHIKV replication, respectively, which points the coordination of amantadine and memantine to Pd(II) as a successful strategy to increase their anti‐CHIKV properties. Conversely, the Pd(II) complexes did not significantly inhibit the replication of ZIKV, which confirms the selectivity towards CHIKV. Interaction of the compounds with N ‐acetyl‐ l ‐cysteine, a model disulfide‐containing peptide, and plasmid DNA pointed to Cys‐containing peptides as more likely targets than nucleotides for the complexes.

ChemistrySelectVol. 9(37)
Instituto Tecnológico de Aeronáutica (BR), Centre National de la Recherche Scientifique (FR), Universidade Estadual de Campinas (UNICAMP) (BR), Universidade Federal do Tocantins (BR), Institut des Sciences Analytiques et de Physico-Chimie pour l'Environnement et les Matériaux (FR), Donostia International Physics Center (ES), Universidade Federal de Uberlândia (BR), Universidade Estadual Paulista (Unesp) (BR)
“la Caixa” Foundation, Fundação de Amparo à Pesquisa do Estado de São Paulo, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Conselho Nacional de Desenvolvimento Científico e Tecnológico, Fundação de Amparo à Pesquisa do Estado de Minas Gerais, H2020 European Research Council
Openalex Percentile: Top 36%
HIV/AIDS drug development and treatment
0.39
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