Structure-activity relationship studies of ME1111, a novel antifungal agent for topical treatment of onychomycosis
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Updated: Jun 7, 2025

Broth Microdilution In Vitro Screening: An Easy and Fast Method to Detect New Antifungal Compounds
Published on: February 14, 2018
Naomi Takei-Masuda1, Maiko Iida2, Makoto Ohyama2
1Meiji Seika Pharma Co. Ltd, Chuo-ku, Tokyo, Japan. naomi.takei@meiji.com.
Abstract:
Onychomycosis is a prevalent disease in many areas of the world, affecting approximately 5.5% of the global population. Among several subtypes of onychomycosis, distal-lateral-subungual onychomycosis is the most common, and topical onychomycosis agents effective against this pathogenesis require properties such as high nail penetration and low affinity for keratin, the main component of the nail. To develop novel and highly effective antifungal agents with such properties, we first established an efficient ex vivo evaluation method using bovine hoof slices and human nails, and then used this method to screen an in-house compound library. Using this strategy, we identified 1, a structure with a phenyl-pyrazole skeleton. In subsequent analyses, we investigated the structure-activity relationship of 1, permitting the identification of 28 (Development Code ME1111).
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