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Inhibitory effects against SARSCoV-2 main protease (Mpro) of biflavonoids and benzophenones from the fruit of Platonia insignis.
Moreira Costa, Monalisa A; de Sousa, Natália F; Mansur Pontes, Carime L; Scotti, Marcus T; de Assis, Francisco F; Braga, Antonio L; Sandjo, Louis P.
Afiliação
  • Moreira Costa MA; Department of Chemistry, CFM, Universidade Federal de Santa Catarina, Campus Universitário-Trindade, Florianópolis 88040-900, SC, Brazil.
  • de Sousa NF; Department of Chemistry, Center for Exact and Natural Sciences, Universidade Federal de Paraíba, Campus I, João Pessoa, PB, Brazil.
  • Mansur Pontes CL; Department of Chemistry, CFM, Universidade Federal de Santa Catarina, Campus Universitário-Trindade, Florianópolis 88040-900, SC, Brazil.
  • Scotti MT; Department of Chemistry, Center for Exact and Natural Sciences, Universidade Federal de Paraíba, Campus I, João Pessoa, PB, Brazil.
  • de Assis FF; Department of Chemistry, CFM, Universidade Federal de Santa Catarina, Campus Universitário-Trindade, Florianópolis 88040-900, SC, Brazil.
  • Braga AL; Department of Chemistry, CFM, Universidade Federal de Santa Catarina, Campus Universitário-Trindade, Florianópolis 88040-900, SC, Brazil.
  • Sandjo LP; Department of Chemistry, CFM, Universidade Federal de Santa Catarina, Campus Universitário-Trindade, Florianópolis 88040-900, SC, Brazil. Electronic address: p.l.sandjo@ufsc.br.
Fitoterapia ; 173: 105784, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38128621
ABSTRACT
The SARS-CoV-2 mutation and the limitation of the approved drug against COVID-19 are still a challenge in many country healthcare systems and need to be affronted despite the set of vaccines to prevent this viral infection. To contribute to the identification of new antiviral agents, the present study focused on natural products from an edible fruit with potential inhibitory effects against the SARS-CoV-2 main protease (Mpro). First, LC-ESIMS analysis of Platonia insignis fruits was performed and showed the presence of biflavonoids and benzophenones in the seed and pulp, respectively. Then, maceration and chromatographic purification led to the identification of two triglycerides (1 and 2) alongside chamaejasmine (3) and volkensiflavone (4) from the seed and isogarcinol (5) and cycloxanthochymol (6), from the pulp. Compounds 1-6 after evaluating their inhibitory against Mpro, displayed from no to significant activity. Compound 5 was the most potent with an IC50 value of 0.72 µM and was more active than the positive control, Ebselen (IC50 of 3.4 µM). It displayed weak and no cytotoxicity against THP-1 (CC50 of 116.2 µM) and Vero cell lines, respectively. Other active compounds showed no cytotoxicity against THP-1. and Vero cell lines. Molecular docking studies revealed interactions in the catalytic pocket between compound 5 and amino acid residues that composed the catalytic dyads (His 41 and Cyst 145).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Biflavonoides / Frutas Idioma: En Revista: Fitoterapia Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Biflavonoides / Frutas Idioma: En Revista: Fitoterapia Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil País de publicação: Holanda