Affiliation:
1. Department of Medical Microbiology and Infectious Diseases, Erasmus MC University Medical Center Rotterdam Dr. Molewaterplein 40 3015 GD Rotterdam, The Netherlands
2. School of Pharmacy University College London London WC1N 1AX United Kingdom
3. Organic Chemistry Laboratory University Bayreuth Universitätsstrasse 30 95440 Bayreuth Germany
Abstract
AbstractEumycetoma, the fungal form of the neglected tropical disease mycetoma, is a crippling infectious disease with low response rates to currently available antifungal drugs. In this study, a series of natural naphthoquinones and anthraquinones was evaluated for their activity against Madurella mycetomatis, which is the most common causative agent of eumycetoma. The metabolic activity of Madurella mycetomatis as well as the viability of Galleria mellonella larvae upon treatment with quinones was investigated. Several hydroxy‐substituted naphthoquinones exhibited activity against Madurella mycetomatis. In particular, naphthazarin (5,8‐dihydroxy‐1,4‐naphthoquinone) was identified as a considerably active antifungal compound against Madurella mycetomatis (IC50=1.4 μM), while it showed reduced toxicity to Galleria mellonella larvae, which is a well‐established in vivo invertebrate model for mycetoma drug studies.
Subject
Molecular Biology,Molecular Medicine,General Chemistry,Biochemistry,General Medicine,Bioengineering
Cited by
3 articles.
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