With heimionones A-E (-), five new terpenoids were isolated from submerged cultures of sp. in addition to the previously described compounds hispidin, hypholomin B, and heimiomycins A and B. Planar structures of the metabolites were elucidated by 1D and 2D NMR in addition to HRESIMS data. While ROESY data assigned relative configurations, absolute configurations were determined by the synthesis of MTPA esters of , , and . The [6.3.0] undecane core structure of compounds - is of the asteriscane-type, however, the scaffold of and with their bicyclo [5.3.0] decane core and germinal methyl substitution is, to our knowledge, unprecedented. Together with several new compounds that were previously isolated from solid cultures of this strain, sp. showed an exceptionally high chemical diversity of its secondary metabolite profile.
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http://dx.doi.org/10.3390/molecules28093723 | DOI Listing |
Molecules
April 2023
Department of Microbial Drugs, Helmholtz Center for Infection Research (HZI), German Center for Infection Research (DZIF), Partner Site Hannover/Braunschweig, Inhoffenstrasse 7, 38124 Braunschweig, Germany.
With heimionones A-E (-), five new terpenoids were isolated from submerged cultures of sp. in addition to the previously described compounds hispidin, hypholomin B, and heimiomycins A and B. Planar structures of the metabolites were elucidated by 1D and 2D NMR in addition to HRESIMS data.
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