Sesquiterpenoids from the <i>Homalomena occulta</i> (Lour.) Schott and their anti-osteoclast genesis activity

Seventeen sesquiterpenoids were isolated from the aerial part of <i>Homalomena occulta</i> (Lour.) Schott. Two new compounds, Homoccusions A (<b>1</b>) and B (<b>2</b>), were determined by extensive spectroscopic methods, ECD calculations, as well as MS analysis. Then, the anti-osteoclast genesis effects of all compounds were studied and compounds <b>1-5</b> showed strong inhibition with an osteoclast genesis inhibitory ratio of over 90% at 10 μM.

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Publication Details

Journal
Natural Product Research
Published
2025-06-11
DOI
https://doi.org/10.1080/14786419.2025.2512565
Primary Topic
Plant Toxicity and Pharmacological Properties
Type
article
Field-Weighted Citation Impact
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article

Sesquiterpenoids from the Homalomena occulta (Lour.) Schott and their anti-osteoclast genesis activity

Sicong Jiang, Tao Tang, Cheng Jiang, Bin Zhao et al.
Natural Product Research
Plant Toxicity and Pharmacological Properties
article

Sesquiterpenoids from the Homalomena occulta (Lour.) Schott and their anti-osteoclast genesis activity

Sicong Jiang, Tao Tang, Cheng Jiang, Bin Zhao, Yi Wu, Yuping Jiang
article en

Abstract

Seventeen sesquiterpenoids were isolated from the aerial part of <i>Homalomena occulta</i> (Lour.) Schott. Two new compounds, Homoccusions A (<b>1</b>) and B (<b>2</b>), were determined by extensive spectroscopic methods, ECD calculations, as well as MS analysis. Then, the anti-osteoclast genesis effects of all compounds were studied and compounds <b>1-5</b> showed strong inhibition with an osteoclast genesis inhibitory ratio of over 90% at 10 μM.

Natural Product Research
Jiujiang University (CN)
Openalex Percentile: Top 88%
Plant Toxicity and Pharmacological Properties
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Sesquiterpenoids from the <i>Homalomena occulta</i> (Lour.) Schott and their anti-osteoclast genesis activity — Sicong Jiang, Tao Tang, et al. · Natural Product Research (2025) | TGRS Research Map | TGRS