An urgent need exists for new antifungal compounds to treat fungal infections in immunocompromised patients.The aim of the current study was to investigate the potency of a novel antifungal compound, MYC-053, against the emerging yeast and yeast-like pathogens Candida glabrata, Candida auris, Cryptococcus neoformans, and Pneumocystis spp.MYC-053 was equally effective against the susceptible control strains, clin. isolates, and resistant strains, with the min. inhibitory concentrations (MIC) of 0.125-4.0μg/mL.Notably, unlike other antifungal compounds, MYC-053 was effective against Pneumocystis isolates.MYC-053 was highly effective against preformed 48-h-old yeast biofilms, with the minimal biofilm eradication concentrations equal to 1-4 times MIC.The compound was not cytotoxic against L2 and A549 cell lines at concentrations over 100μg/mL.Further, it possessed no apparent hemolytic activity up to 1000μg/mL (the highest concentration tested).Overall, these data indicated that MYC-053 has a broad therapeutic window and may be developed into a promising antifungal agent for the treatment and prevention of invasive fungal infections caused by yeasts and yeast-like fungi in neutropenic patients.