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J Nat Prod ; 85(10): 2363-2371, 2022 10 28.
Article in English | MEDLINE | ID: mdl-36130285

ABSTRACT

Seven sesquiterpenoids, named nebucanes A-G (1-7), featuring a rare alliacane scaffold with unprecedented furan or pyrrole functions, were isolated from the fermentation broth of Clitocybe nebularis. Their structures were established on the basis of 1D/2D NMR spectroscopic analyses, HR-(+)-ESIMS spectra, and comparison of measured and calculated CD spectra for determination of the absolute configuration. Assessing the biological activities, nebucane D (4) exhibited antifungal effects against Rhodotorula glutinis, while nebucane G (7) displayed significant cytotoxicity against MCF-7 and A431 cell lines.


Subject(s)
Agaricales , Basidiomycota , Sesquiterpenes , Agaricales/chemistry , Basidiomycota/chemistry , Sesquiterpenes/chemistry , Antifungal Agents , Molecular Structure
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