Two new naphthopyrones and a new prenylisoflavone from Berchemia lineata

Two new naphthopyrones, berchelineatones A and B ( 1 and 2 ), together with a new prenylisoflavone ( 3 ), were isolated from Berchemia lineata . Their structures were primarily determined by high-resolution mass spectrometry, NMR spectroscopy, and X-ray crystallographic data analysis. Notably, compounds 1 and 2 exhibited potent inhibition on nitric oxide (NO) production induced by lipopolysaccharide (LPS) in RAW264.7 macrophages, with IC 50 values of 2.52 and 2.06 μ M, respectively. • Two new naphthopyrones and a new prenylisoflavone were isolated from Berchemia lineata . • The structures were elucidated by spectroscopic and X-ray crystallographic data analysis. • Berchelineatones A and B exhibited significant NO inhibitory activity.

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Publication Details

Journal
Phytochemistry Letters
Published
2026-01-05
DOI
https://doi.org/10.1016/j.phytol.2026.104111
Primary Topic
Bioactive natural compounds
Type
article
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article

Two new naphthopyrones and a new prenylisoflavone from Berchemia lineata

De-an Guo, Weilin Qiao, Ling Li, Lihua Peng et al.
Phytochemistry Letters
Bioactive natural compounds
article

Two new naphthopyrones and a new prenylisoflavone from Berchemia lineata

De-an Guo, Weilin Qiao, Ling Li, Lihua Peng, Lin Feng, Wei Li
article en

Abstract

Two new naphthopyrones, berchelineatones A and B ( 1 and 2 ), together with a new prenylisoflavone ( 3 ), were isolated from Berchemia lineata . Their structures were primarily determined by high-resolution mass spectrometry, NMR spectroscopy, and X-ray crystallographic data analysis. Notably, compounds 1 and 2 exhibited potent inhibition on nitric oxide (NO) production induced by lipopolysaccharide (LPS) in RAW264.7 macrophages, with IC 50 values of 2.52 and 2.06 μ M, respectively. • Two new naphthopyrones and a new prenylisoflavone were isolated from Berchemia lineata . • The structures were elucidated by spectroscopic and X-ray crystallographic data analysis. • Berchelineatones A and B exhibited significant NO inhibitory activity.

Phytochemistry LettersVol. 71
Zunyi Medical University (CN), Chinese Academy of Sciences (CN), Shanghai Institute of Materia Medica (CN), Zhongshan Hospital (CN)
Openalex Percentile: Top 97%
Bioactive natural compounds
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