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Propyl (E)-3-(furan-2-yl) Acrylate: a synthetic antifungal potential with a regulatory effect on the biosynthesis of ergosterol in Candida Albicans
Costa, Paulo César Trindade da; Santos, Thales Luciano Bezerra; Ramos, Jaqueline Ferreira; Santos, Jonh Anderson Macêdo; Medeiros, Francinalva Dantas de; Freitas, Juliano Carlo Rufino de; Oliveira, Wylly Araújo de.
  • Costa, Paulo César Trindade da; Federal University of Campina Grande. Education and health department. Cuité. BR
  • Santos, Thales Luciano Bezerra; Federal University of Campina Grande. Education and health department. Cuité. BR
  • Ramos, Jaqueline Ferreira; Rural Federal University of Pernambuco. Chemistry department. Recife. BR
  • Santos, Jonh Anderson Macêdo; Rural Federal University of Pernambuco. Chemistry department. Recife. BR
  • Medeiros, Francinalva Dantas de; Federal University of Campina Grande. Education and health department. Cuité. BR
  • Freitas, Juliano Carlo Rufino de; Federal University of Campina Grande. Education and health department. Cuité. BR
  • Oliveira, Wylly Araújo de; Federal University of Campina Grande. Education and health department. Cuité. BR
Braz. J. Pharm. Sci. (Online) ; 59: e22045, 2023. tab, graf
Article in English | LILACS | ID: biblio-1439519
ABSTRACT
Abstract The genus Candida represents the main cause of infections of fungal origin. Some species stand out as disease promoters in humans, such as C. albicans, C. glabrata, C. parapsilosis, and C. tropicalis. This study evaluated the antifungal effects of propyl (E)-3-(furan-2-yl) acrylate. The minimum inhibitory concentration of the synthetic compound, amphotericin B and fluconazole alone against four species of Candida ranged from 64 to 512 µg/mL, 1 to 2 µg/mL, and 32 to 256 µg/mL, respectively. The synergistic effect of the test substance was observed when associated with fluconazole against C. glabrata, there was no antagonism between the substances against any of the tested strains. The potential drug promoted morphological changes in C. albicans, decreasing the amount of resistance, virulence, and reproduction structures, such as the formation of pseudohyphae, blastoconidia, and chlamydospores, ensuring the antifungal potential of this substance. It was also possible to identify the fungicidal profile of the test substance through the study of the growth kinetics of C. albicans. Finally, it was observed that the test compound inhibited the ergosterol biosynthesis by yeast
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Full text: Available Index: LILACS (Americas) Main subject: Candida albicans / Ergosterol / Antifungal Agents Language: English Journal: Braz. J. Pharm. Sci. (Online) Journal subject: Farmacologia / Terapˆutica / Toxicologia Year: 2023 Type: Article Affiliation country: Brazil Institution/Affiliation country: Federal University of Campina Grande/BR / Rural Federal University of Pernambuco/BR

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Full text: Available Index: LILACS (Americas) Main subject: Candida albicans / Ergosterol / Antifungal Agents Language: English Journal: Braz. J. Pharm. Sci. (Online) Journal subject: Farmacologia / Terapˆutica / Toxicologia Year: 2023 Type: Article Affiliation country: Brazil Institution/Affiliation country: Federal University of Campina Grande/BR / Rural Federal University of Pernambuco/BR