“…22 Even before they were known as inhibitors of histone and DNA methyltransferases, agents such as trichostatin A (TSA) and 5-azacytidine (5-AC) were initially shown to have a role in fungal development and other processes in several different species of fungi, including C. albicans, Aspergillus spp., F. oxysporum, and N. crassa. 36,[113][114][115][116][117][118][119][120] Their application in development applies to metazoans as well, as many HDAC and DNMT inhibitors were discovered in a screen for anticancer agents, and have since progressed to clinical testing. 20,22 Combinations of nine different HDAC and DNMT inhibitors against twelve different fungi, including A. flavus, A. westerdijkiae, Cladosporium cladosporoides, Clonostachys sp., Diatrype sp., Penicillium chrysogenum, Penicillium citrinum, Rhizopus sp., Verticillium psallotae, and three unknown filamentous fungi resulted in altered metabolite profiles under at least one condition.…”