An integrated in silico and in vitro approach for the identification of natural products tyrosinase inhibitors

Uma abordagem integrada in silico e in vitro para a identificação de produtos naturais inibidores da tirosinase

Autores

  • Nathan Ezequiel Chaves Universidade Comunitária da Região de Chapecó
  • Daniela Miorando
  • Aline Mânica
  • Walter Antonio Roman Junior Universidade Comunitária da Região de Chapecó - Unochapecó

DOI:

https://doi.org/10.53660/CLM-3324-24H35

Palavras-chave:

Medicinal plants, Flavonoids, Virtual screening, Melanin, Cytotoxicity

Resumo

The biosynthesis of melanin, the main protein involved in skin pigmentation, involves tyrosine, the enzyme tyrosinase, and ultraviolet radiation. However, an imbalance in this process can promote cutaneous hypermelanosis (CH), which causes spots on the skin. The CH treatment involves techniques and products with high adverse reactions. In this context, research has been increased into natural products. However, investigations using computational tools combined with evaluations of enzyme inhibition (in vitro) and toxicity tests are scarce. In this study, we evaluated thirteen bioactive compounds using virtual screening (SwissADME and SwissTarget Prediction software), and the most promising molecules were tested for tyrosinase inhibitory effects and cytotoxicity assays (MTT). Kaempferol, apigenin, and quercetin revealed better in silico bioavailability and tyrosinase inhibition parameters (94.8, 91.9, and 88.4%, respectively). Additionally, these molecules demonstrated different cytotoxicity profiles at 24 and 48 hours of exposure. Our evidence indicates that the flavonoids tested are promising agents in inhibiting tyrosinase.

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Publicado

2024-04-27

Como Citar

Chaves, N. E., Miorando, D., Mânica, A., & Roman Junior, W. A. (2024). An integrated in silico and in vitro approach for the identification of natural products tyrosinase inhibitors: Uma abordagem integrada in silico e in vitro para a identificação de produtos naturais inibidores da tirosinase. Concilium, 24(8), 148–162. https://doi.org/10.53660/CLM-3324-24H35

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