New Duclauxamide from Penicillium manginii YIM PH30375 and Structure Revision of the Duclauxin Family

Duclauxamide A1 (1), a new polyketide-derived heptacyclic oligophenalenone dimer with a N-2-hydroxyethyl moiety, was isolated from Penicillium manginii YIM PH30375. Spectroscopic analysis, X-ray single crystal diffraction, and ¹³C NMR DFT calculations confirmed that compound 1 and other duclauxin analogues possess the unified S configuration at C-9′, which corrects a long-standing misrepresentation of duclauxins as C-9′R epimers. A plausible biosynthetic pathway for duclauxins is proposed on the basis of previous acetate labeling results for duclauxin and sclerodin.