Phanerochanols A–C: identification and biological evaluation of metabolites from the mushroom-associated fungus <i>Phanerochaete sp</i> . GLQ06

The fungal strain <i>Phanerochaete sp.</i> GLQ06 was successfully isolated from the fresh fruiting bodies of <i>Ganoderma applanatum</i>. Through systematic chemical investigation, three new natural products were obtained from this fungal source: phanerochanol A (<b>1</b>) along with two new stachyline derivatives designated as phanerochanols B (<b>2</b>) and C (<b>3</b>). Their structures were elucidated using NMR spectroscopic data and ECD calculations. Biological evaluation results revealed that compounds <b>1</b>, <b>3</b>, and <b>5</b> exhibited anti-inflammatory activity by inhibiting nitric oxide (NO) production in LPS-activated RAW 264.7 cells. Specifically, compound <b>1</b> demonstrated a significant inhibitory effect on NO production, surpassing that of dexamethasone at 10 μM, while no substantial cytotoxicity was observed within the tested concentration range.

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Journal
Natural Product Research
Published
2025-06-28
DOI
https://doi.org/10.1080/14786419.2025.2525584
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
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article

Phanerochanols A–C: identification and biological evaluation of metabolites from the mushroom-associated fungus Phanerochaete sp . GLQ06

Meng Shao, Zhenyu Liu, Enwei Tian, Gui-Hu Lu et al.
Natural Product Research
Microbial Natural Products and Biosynthesis
article

Phanerochanols A–C: identification and biological evaluation of metabolites from the mushroom-associated fungus Phanerochaete sp . GLQ06

Meng Shao, Zhenyu Liu, Enwei Tian, Gui-Hu Lu, Qi Luo, Jia-Hao Xue, Xin-Huan Qiu
article en

Abstract

The fungal strain <i>Phanerochaete sp.</i> GLQ06 was successfully isolated from the fresh fruiting bodies of <i>Ganoderma applanatum</i>. Through systematic chemical investigation, three new natural products were obtained from this fungal source: phanerochanol A (<b>1</b>) along with two new stachyline derivatives designated as phanerochanols B (<b>2</b>) and C (<b>3</b>). Their structures were elucidated using NMR spectroscopic data and ECD calculations. Biological evaluation results revealed that compounds <b>1</b>, <b>3</b>, and <b>5</b> exhibited anti-inflammatory activity by inhibiting nitric oxide (NO) production in LPS-activated RAW 264.7 cells. Specifically, compound <b>1</b> demonstrated a significant inhibitory effect on NO production, surpassing that of dexamethasone at 10 μM, while no substantial cytotoxicity was observed within the tested concentration range.

Natural Product Research
Southern Medical University (CN)
Zero hunger
Openalex Percentile: Top 83%
Microbial Natural Products and Biosynthesis
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