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Evaluation of Thiazolidine Derivatives with Potential Anti-ZIKV Activity.
Maria Calado Gonçalves, Sayonara; Vieira Galdino, Lília; Costa Lima, Morganna; da Silva Moura, José Arion; Carvalho Francisco Viana, Douglas; Melgarejo da Rosa, Michelle; Gomes Rebello Ferreira, Luiz Felipe; Zaldini Hernandes, Marcelo; Cristiny Pereira, Michelly; Barreto de Melo Rêgo, Moacyr Jesus; da Rocha Pitta, Ivan; de Oliveira França, Rafael; Galdino da Rocha Pitta, Marina; Galdino da Rocha Pitta, Maira.
Afiliação
  • Maria Calado Gonçalves S; Therapeutic Innovation Research Center, Federal University of Pernambuco, Av. Moraes Rego, 1235, Recife, 50670-901, Brazil.
  • Vieira Galdino L; Therapeutic Innovation Research Center, Federal University of Pernambuco, Av. Moraes Rego, 1235, Recife, 50670-901, Brazil.
  • Costa Lima M; Department of Virology and Experimental Therapy, Aggeu Magalhães Institute, Oswaldo Cruz Foundation / FIOCRUZ, Av. Moraes Rego, 1235, Recife, 50670-901, Brazil.
  • da Silva Moura JA; Pharmaceutical Planning and Synthesis Laboratory, Federal University of Pernambuco Av. Moraes Rego, 1235, Recife, 50670-901, Brazil.
  • Carvalho Francisco Viana D; Pharmaceutical Planning and Synthesis Laboratory, Federal University of Pernambuco Av. Moraes Rego, 1235, Recife, 50670-901, Brazil.
  • Melgarejo da Rosa M; Therapeutic Innovation Research Center, Federal University of Pernambuco, Av. Moraes Rego, 1235, Recife, 50670-901, Brazil.
  • Gomes Rebello Ferreira LF; Department of Pharmaceutical Sciences, Federal University of Pernambuco, Av. Prof. Artur de Sá, Recife-PE, 50740-521, Brazil.
  • Zaldini Hernandes M; Department of Pharmaceutical Sciences, Federal University of Pernambuco, Av. Prof. Artur de Sá, Recife-PE, 50740-521, Brazil.
  • Cristiny Pereira M; Therapeutic Innovation Research Center, Federal University of Pernambuco, Av. Moraes Rego, 1235, Recife, 50670-901, Brazil.
  • Barreto de Melo Rêgo MJ; Therapeutic Innovation Research Center, Federal University of Pernambuco, Av. Moraes Rego, 1235, Recife, 50670-901, Brazil.
  • da Rocha Pitta I; Pharmaceutical Planning and Synthesis Laboratory, Federal University of Pernambuco Av. Moraes Rego, 1235, Recife, 50670-901, Brazil.
  • de Oliveira França R; Department of Virology and Experimental Therapy, Aggeu Magalhães Institute, Oswaldo Cruz Foundation / FIOCRUZ, Av. Moraes Rego, 1235, Recife, 50670-901, Brazil.
  • Galdino da Rocha Pitta M; Pharmaceutical Planning and Synthesis Laboratory, Federal University of Pernambuco Av. Moraes Rego, 1235, Recife, 50670-901, Brazil.
  • Galdino da Rocha Pitta M; Therapeutic Innovation Research Center, Federal University of Pernambuco, Av. Moraes Rego, 1235, Recife, 50670-901, Brazil.
Curr Top Med Chem ; 2024 Aug 12.
Article em En | MEDLINE | ID: mdl-39136505
ABSTRACT

OBJECTIVE:

In this study, we have synthesized 19 Thiazolidine (TZD) derivatives to investigate their potential anti-ZIKV effects.

METHODS:

Nineteen thiazolidine derivatives were synthesized and evaluated for their cytotoxicity and antiviral activity against the ZIKA virus.

RESULTS:

Among them, six demonstrated remarkable selectivity against the ZIKV virus, exhibiting IC50 values of <5µM, and the other compounds did not demonstrate selectivity for the virus. Interestingly, several derivatives effectively suppressed the replication of ZIKV RNA copies, with derivatives significantly reducing ZIKV mRNA levels at 24 hours post-infection (hpi). Notably, two derivatives (ZKC-4 and -9) stood out by demonstrating a protective effect against ZIKV cell entry. Informed by computational analysis of binding affinity and intermolecular interactions within the NS5 domain's N-7 and O'2 positions, ZKC-4 and FT-39 displayed the highest predicted affinities. Intriguingly, ZKC-4 and ZKC-9 derivatives exhibited the most favorable predicted binding affinities for the ZIKV-E binding site.

CONCLUSION:

The significance of TZDs as potent antiviral agents is underscored by these findings, suggesting that exploring TZD derivatives holds promise for advancing antiviral therapeutic strategies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Curr Top Med Chem Assunto da revista: QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil País de publicação: Emirados Árabes Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Curr Top Med Chem Assunto da revista: QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil País de publicação: Emirados Árabes Unidos