Abstract
Quadristerols A−G, seven undescribed ergosterols, were obtained from Aspergillus quadrilineata. Their structures and absolute configurations were determined based on HRESIMS, NMR, quantum-chemical calculations, and single-crystal X-ray diffraction analyses. Quadristerols A−G featured ergosterol skeletons with different attachments; quadristerols A−C were three diastereoisomers possessing a 2-hydroxy-propionyloxy group at C-6, and quadristerols D−G were two pairs of epimers with a 2,3-butanediol group at C-6. All of these compounds were evaluated for their immunosuppressive activities in vitro. Quadristerols B and C showed excellent inhibitory effects against concanavalin A-induced T lymphocyte proliferation with IC50 values of 7.43 and 3.95 μM, respectively, and quadristerols D and E strongly inhibited lipopolysaccharide-induced B lymphocyte proliferation with IC50 values of 10.96 and 7.47 μM, respectively.
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