RSC medicinal chemistry · 2025
Structure-activity relationships of fenarimol analogues with potent in vitro and in vivo activity against Madurella mycetomatis, the main causative agent of mycetoma.
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Duong Hung Phat, Melechov Dmitrij, Lim Wilson, Ma Jingyi, Scroggie Kymberley R, Rajendra Luxsika, Perry Benjamin, Cruz Luiza R, Saleem Rahman Shah Zaib, Rutledge Peter J, Motion Alice, van de Sande Wendy W J, Todd Matthew H
Аннотация
The fenarimol analogue EPL-BS1246 was previously discovered to be potent against Madurella mycetomatis, the causative agent of the neglected tropical disease mycetoma. Further evaluation of a small set of fenarimol analogues in vivo revealed a correlation between efficacy and the lipophilicity (log D) of the analogues. To explore both this correlation and the series structure-activity relationship (SAR), we have evaluated a total of 185 fenarimol analogues derived from five different daughter chemotypes. Potent (MIC50 < 9 μM) in vitro activity was found for 22 analogues, five of which gave promising results in an in vivo larval survival assay. Again, a trend towards prolonged larval survival (better in vivo activity) was noted in analogues with log D values <2.5. Insights into the SAR could be gleaned that suggested optimal substituents for the rings forming the fenarimol core.