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Molecules 2011, 16(8), 6422-6431; doi:10.3390/molecules16086422
Article

Alkylphenol Activity against Candida spp. and Microsporum canis: A Focus on the Antifungal Activity of Thymol, Eugenol and O-Methyl Derivatives

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Received: 11 May 2011; in revised form: 15 July 2011 / Accepted: 26 July 2011 / Published: 29 July 2011
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Abstract: In recent years there has been an increasing search for new antifungal compounds due to the side effects of conventional antifungal drugs and fungal resistance. The aims of this study were to test in vitro the activity of thymol, eugenol, estragole and anethole and some O-methyl-derivatives (methylthymol and methyleugenol) against Candida spp. and Microsporum canis. The broth microdilution method was used to determine the minimum inhibitory concentration (MIC). The minimum fungicidal concentrations (MFC) for both Candida spp. and M. canis were found by subculturing each fungal suspension on potato dextrose agar. Thymol, methylthymol, eugenol, methyl-eugenol, anethole, estragole and griseofulvin respectively, presented the following MIC values against M. canis: 4.8–9.7; 78–150; 39; 78–150; 78–150; 19–39 µg/mL and 0.006–2.5 mg/mL. The MFC values for all compounds ranged from 9.7 to 31 µg/mL. Concerning Candida spp, thymol, methylthymol, eugenol, methyleugenol, anethole, estragole and amphotericin, respectively, showed the following MIC values: 39; 620–1250; 150–620; 310–620; 620; 620–1250 and 0.25–2.0 mg/mL. The MFC values varied from 78 to 2500 µg/mL. All tested compounds thus showed in vitro antifungal activity against Candida spp. and M. canis. Therefore, further studies should be carried out to confirm the usefulness of these alkylphenols in vivo.
Keywords: thymol; eugenol; estragole; methyl-derivatives; dermathophytes; Candida thymol; eugenol; estragole; methyl-derivatives; dermathophytes; Candida
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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MDPI and ACS Style

Fontenelle, R.O.; Morais, S.M.; Brito, E.H.; Brilhante, R.S.; Cordeiro, R.A.; Lima, Y.C.; Brasil, N.V.; Monteiro, A.J.; Sidrim, J.J.; Rocha, M.F. Alkylphenol Activity against Candida spp. and Microsporum canis: A Focus on the Antifungal Activity of Thymol, Eugenol and O-Methyl Derivatives. Molecules 2011, 16, 6422-6431.

AMA Style

Fontenelle RO, Morais SM, Brito EH, Brilhante RS, Cordeiro RA, Lima YC, Brasil NV, Monteiro AJ, Sidrim JJ, Rocha MF. Alkylphenol Activity against Candida spp. and Microsporum canis: A Focus on the Antifungal Activity of Thymol, Eugenol and O-Methyl Derivatives. Molecules. 2011; 16(8):6422-6431.

Chicago/Turabian Style

Fontenelle, Raquel O.S.; Morais, Selene M.; Brito, Erika H.S.; Brilhante, Raimunda S.N.; Cordeiro, Rossana A.; Lima, Ynayara C.; Brasil, Nilce V.G.P.S.; Monteiro, André J.; Sidrim, José J.C.; Rocha, Marcos F.G. 2011. "Alkylphenol Activity against Candida spp. and Microsporum canis: A Focus on the Antifungal Activity of Thymol, Eugenol and O-Methyl Derivatives." Molecules 16, no. 8: 6422-6431.



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