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Investigation of the soil-derived fungus  Lasiodiplodia theobromae  NSTRU-PN1.4 resulted in the isolation of five dimeric γ-lactones including two new botryosphaerilactones D and E ( 4  and  5 ) and three known structurally related analogoues ( 1–3 ) along with seven known compounds. Their structures were elucidated by extensive spectroscopic analysis. The absolute configuration of  1–5  was determined by comparison of the ECD data with those of the structurally related monomeric γ-lactones. For biological evaluation, this is the first report on antifungal activity of the known (3  R ,4 R )-4-acetyl-3-methyl-2(3 H )-dihydrofuranone which displayed weak antifungal activity against  Cryptococcus neoformans  with an MIC value of 200 µg/mL.

Dimeric γ-lactone derivatives from the soil-derived fungus Lasiodiplodia theobromae NSTRU-PN1.4