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Given that many antifungal medications are susceptible to evolved resistance, there is a need for novel drugs with unique mechanisms of action. Inhibiting the essential proton pump Pma1p, a P-type ATPase, is a potentially effective therapeutic approach that is orthogonal to existing treatments. We identify NSC11668 and hitachimycin as structurally distinct antifungals that inhibit yeast  Sc Pma1p. These compounds provide new opportunities for drug discovery aimed at this important target.Electronic supplementary material  The online version of this article (10.1186/s13321-018-0261-3) contains supplementary material, which is available to authorized users.

Two inhibitors of yeast plasma membrane ATPase 1 (ScPma1p): toward the development of novel antifungal therapies