Two New Chromone Derivatives from a Marine Algicolous Fungus Aspergillus versicolor GXIMD 02518 and Their Osteoclastogenesis Inhibitory Activity

Two new chromone derivatives, cnidimols I and J (<b>1</b> and <b>2</b>), together with ten known aromatic derivatives (<b>3</b>-<b>12</b>), were isolated from the Beibu Gulf algicolous fungus <i>Aspergillus versicolor</i> GXIMD 02518. Their structures were determined by comprehensive physicochemical and spectroscopic data interpretation. The absolute configurations of <b>1</b> and <b>2</b> were accomplished by ECD calculations and X-ray diffraction analysis. Compound <b>1</b> was obtained as a pair of enantiomers, which were separated by chiral-phase HPLC analysis. Notably, 3,7-dihydroxy-1,9-dimethyldibenzofuran (<b>6</b>) displayed significant inhibition in LPS-induced NF-κB luciferase activity in RAW 264.7 macrophages, which further inhibited RANKL-induced osteoclast differentiation without cytotoxicity in bone marrow macrophage cells.

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Publication Details

Journal
Marine Drugs
Published
2025-11-07
DOI
https://doi.org/10.3390/md23110429
Citations
1
Primary Topic
Bone Metabolism and Diseases
Type
article
Field-Weighted Citation Impact
0.81

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article

Two New Chromone Derivatives from a Marine Algicolous Fungus Aspergillus versicolor GXIMD 02518 and Their Osteoclastogenesis Inhibitory Activity

Zongjin Li, Xiaowei Luo, Humu Lu, Shuai Peng et al.
1 citations
Marine Drugs
Bone Metabolism and Diseases
0.81
article

Two New Chromone Derivatives from a Marine Algicolous Fungus Aspergillus versicolor GXIMD 02518 and Their Osteoclastogenesis Inhibitory Activity

Zongjin Li, Xiaowei Luo, Humu Lu, Shuai Peng, Miaoping Lin, Chenghai Gao, Yonghong Liu, Xin Qi, Hongling Qin
article en
1 citations

Abstract

Two new chromone derivatives, cnidimols I and J (<b>1</b> and <b>2</b>), together with ten known aromatic derivatives (<b>3</b>-<b>12</b>), were isolated from the Beibu Gulf algicolous fungus <i>Aspergillus versicolor</i> GXIMD 02518. Their structures were determined by comprehensive physicochemical and spectroscopic data interpretation. The absolute configurations of <b>1</b> and <b>2</b> were accomplished by ECD calculations and X-ray diffraction analysis. Compound <b>1</b> was obtained as a pair of enantiomers, which were separated by chiral-phase HPLC analysis. Notably, 3,7-dihydroxy-1,9-dimethyldibenzofuran (<b>6</b>) displayed significant inhibition in LPS-induced NF-κB luciferase activity in RAW 264.7 macrophages, which further inhibited RANKL-induced osteoclast differentiation without cytotoxicity in bone marrow macrophage cells.

Marine DrugsVol. 23(11)
Hunan University (CN), Guangxi University of Chinese Medicine (CN)
National Natural Science Foundation of China, Natural Science Foundation of Guangxi Province, Guangxi University
Openalex Percentile: Top 22%
Bone Metabolism and Diseases
0.81
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