The therapeutic landscape for mycotic infections is shifting. New generatio
n azoles that are active against clinically relevant, drug-resistant fungal
pathogens have improved bioavailability, half-lives and safety profiles. A
cylated cyclic peptide inhibitors of beta (1,3)glucan synthesis with origin
s as fungal metabolites provide an alternative and highly-selective mode of
action, targeting cell-wall biogenesis in important pathogens such as Cand
ida and Aspergillus species. The development, in each structural class, of
compounds that have advanced to late-stage clinical trials is summarized in
this review.