1993
DOI: 10.1007/bf02898762
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Relationship between antifungal activity and hydrophobicity of kojic acid derivatives

Abstract: Twenty three kojic acid derivatives were tested in the agar diffusion test against twenty five dermatophytic fungi. The inhibitory effects at equal doses (10 mg/L) were correlated with the 1-octanol-water partition coefficients of the compounds. An improvement in antifungal activity can be achieved by increasing the hydrophobicity of the compounds.

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Cited by 24 publications
(5 citation statements)
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“…The antimicrobial activity of KA and its derivatives against a number of microorganisms was reported previously; 29,45,48,62,63 there are no similar reports in the literature for KA nanocomposites. Incorporating other derivatives of KA of higher antibacterial activity may also reveal additional information towards understanding the antimicrobial activity of KA-polymer-nanocomposites and their applications.…”
Section: In Vitro Antimicrobial Activity Of the Ka Nanocompositesmentioning
confidence: 76%
“…The antimicrobial activity of KA and its derivatives against a number of microorganisms was reported previously; 29,45,48,62,63 there are no similar reports in the literature for KA nanocomposites. Incorporating other derivatives of KA of higher antibacterial activity may also reveal additional information towards understanding the antimicrobial activity of KA-polymer-nanocomposites and their applications.…”
Section: In Vitro Antimicrobial Activity Of the Ka Nanocompositesmentioning
confidence: 76%
“…35 Kojic acid was tested in the agar diffusion test against twenty five dermatophytic fungi. 36 The kojic acid has efficiency of whitening, antioxidant and antibacterial. Content of total phenol with antioxidant and antibacterial were relevant.…”
Section: Determination Of Total Phenolic and Kojic Acid Contentmentioning
confidence: 99%
“…The higher cytotoxic activity of methoxyvermistatin, as measured against KB and KBv200 cells (derived from epithelial carcinoma) [ 21 ], also indicates that a remarkable importance pertains to the methoxyl group at the γ-pyrone ring, which also characterizes 3-O-methylfunicone. To this regard, it must be considered that the antifungal activity reported for several derivatives of kojic acid [ 43 ] provides a further indirect evidence that biological properties of funicone-related compounds are in part dependent on the γ-pyrone moiety.…”
Section: Biological Activities Of Funicone-related Compoundsmentioning
confidence: 99%