@article{Huo2025, 
author = {Ruiyun Huo and Yu Tu and Chang Liu and Guangrong Zi and Ying Shi and Jinwei Ren and Lei Cai and Ling Liu},
title = {New antifungal chlorinated orsellinic aldehydes from the deep-sea-derived fungus Acremonium sclerotigenum LW14},
year = {2025},
journal = {Mycology},
volume = {16},
number = {4},
pages = {1797-1806},
keywords = {structure elucidation, antifungal activity, Deep-sea-derived fungus, ECD calculations, NMR calculations},
url = {https://www.sciopen.com/article/10.1080/21501203.2025.2485477},
doi = {10.1080/21501203.2025.2485477},
abstract = {Two new pairs of chlorinated orsellinic aldehyde enantiomers acresorcinols A and B (1a/1b and 2a/2b), and three orsellinic aldehydes, acresorcinols C−E (3−5) were discovered from the extract of the deep-sea-derived fungus Acremonium sclerotigenum LW14. Their structures, including absolute configurations, were experimentally elucidated by spectroscopic analysis, NMR calculations with DP4+ probability analysis, and ECD calculations. Compounds 1 and 2 exemplify the first reported chlorinated orsellinic aldehydes, characterised by a distinctive 6/5−5 tricyclic core structure with a bridged framework. Acresorcinol C (3) was a rare carbon-bridged resorcinol dimer via a methylene bridge. The bioassay results showed that all compounds exhibited antifungal activities against Cryptococcus gattii 3271G1 at 32 μg/mL. Compounds 1−3 showed antifungal effects against C. gattii 3271G1, displaying MIC values of 8, 16, and 16 µg/mL, respectively.}
}