Biological and Pharmaceutical Bulletin
Online ISSN : 1347-5215
Print ISSN : 0918-6158
ISSN-L : 0918-6158
Notes
In Vitro Antifungal Activity of Naphthoquinone Derivatives
Kenroh SasakiHidetomo AbeFumihiko Yoshizaki
Author information
JOURNAL FREE ACCESS

2002 Volume 25 Issue 5 Pages 669-670

Details
Abstract

In vitro antifungal activities of naphtoquinone-derivatives, which are constituents of Shikon, roots of Lithospermum erythrorhizon, were investigated against several fungal pathogens. When the biological activity of these compounds was tested against fungi, a wide range of sensitivity was recorded. Shikonin was found to have a stronger than fluconazole against yeast-like fungi: four-fold against Candida krusei (minimal inhibitory concentration (MIC); 4 μg/ml) and two-fold (MIC; 4 μg/ml) against Saccharomyces cerevisiae, though it showed the same potency as fluconazole against C. glabrata. Deoxyshikonin also exhibited four-fold stronger activity against C. krusei (MIC; 4 μg/ml) and three-fold (MIC; 2 μg/ml) stronger against S. cerevisiae. Acetylshikonin and β-hydroxyisovaleryl shikonin showed lower activities against all fungal pathogens except for C. krusei compared with the standard. Against the filamentous fungus, Trichosporon cutaneum, all naphthoquinones were found to have a range of activity with lower potency than standard. This result provides a rational basis for the clinical use of shikon and shows the possibility of its use in medicinal treatment as an anti-inflammatory agent with antifungal activity.

Content from these authors
© 2002 The Pharmaceutical Society of Japan
Previous article Next article
feedback
Top