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1.
Bioorg Chem ; 108: 104562, 2021 03.
Article in English | MEDLINE | ID: mdl-33358389

ABSTRACT

Twelve undescribed lanostane-type triterpenes, and twenty-two known triterpenes were isolated and identified from a medicinal bracket fungus Fomitopsis pinicola (Sw.) P. Karst. The structures of these compounds were determined by spectroscopic and spectrometric analyses. The antiinflammatory potential of thirty-two triterpene compounds was evaluated using neutrophils as an assay model, and pinicolasin J was the most potent inhibitor of superoxide anion generation and elastase release, with IC50 values of 1.81 ± 0.44 and 2.50 ± 0.64 µM, respectively. This study provides scientific insight into the nutritional supplement value and medicinal development of Fomitopsis pinicola.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Coriolaceae/chemistry , Enzyme Inhibitors/pharmacology , Fruiting Bodies, Fungal/chemistry , Pancreatic Elastase/antagonists & inhibitors , Triterpenes/pharmacology , Anti-Inflammatory Agents/chemistry , Anti-Inflammatory Agents/isolation & purification , Dose-Response Relationship, Drug , Enzyme Inhibitors/chemistry , Enzyme Inhibitors/isolation & purification , Humans , Molecular Structure , Neutrophils/drug effects , Neutrophils/metabolism , Pancreatic Elastase/metabolism , Structure-Activity Relationship , Triterpenes/chemistry , Triterpenes/isolation & purification
2.
RSC Adv ; 9(59): 34184-34195, 2019 Oct 23.
Article in English | MEDLINE | ID: mdl-35530004

ABSTRACT

Twelve undescribed sesquiterpenoids, fomitopins A-L (1-12), were isolated via bioassay-guided purification from the bracket fungus Fomitopsis pinicola (Sw.) P. Karst, and this fungus have been reported to exhibit anti-microbial and anti-inflammatory activities. The structures of 1-12 were elucidated by spectroscopic and spectrometric analyses and their absolute configurations were further confirmed by ECD simulations. Ten isolated compounds were evaluated for their anti-inflammatory potential and compound 11 exhibited the most significant inhibition of superoxide anion generation and elastase release with IC50 values of 0.81 ± 0.15 and 0.74 ± 0.12 µM. These newly purified sesquiterpenoids could be potential candidates for further anti-inflammatory studies.

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