Chemical investigation of the desert soil-derived fungus Aspergillus fumigatus J3-4-1 led to the isolation of two new indole diketopiperazines, fumines A (1) and B (2), along with seven known analogues (3-9). Their structures were elucidated through comprehensive analysis of NMR and HRESIMS data and were further confirmed by electronic circular dichroism (ECD) calculations. All isolated compounds exhibited broad-spectrum antifungal activity against five phytopathogenic fungi at a concentration of 50 µg/mL, with inhibition rates ranging from 12.51% to 88.08%. Notably, compounds 2 and 3 displayed superior activity against A. alternata and A. solani, with IC50 values as low as 7.22 µg/mL, outperforming the commercial fungicide hymexazol. These results highlight the potential of these compounds as promising candidates for the development of new antifungal agents.
Men et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: