A New Methoxyflavonoid Rutinoside and PTP1B-Inhibitory Phenolic Compounds from the Water Extract of Areca catechu L.

Phytochemical investigation of the water extract and alkaloid fraction of Areca catechu L. led to the isolation of one new methoxyflavonoid rutinoside (1), together with eleven known compounds (2−12), five of which (8−12) belong to the pyridine alkaloid class. The structure of the new compound was elucidated through extensive spectroscopic analyses, including 1D and 2D NMR experiments and high-resolution mass spectrometry. Notably, rhamnazin-3-O-rutinoside (2) is reported here for the first time from this species. The isolated compounds were evaluated for their inhibitory activity against protein tyrosine phosphatase 1B (PTP1B) using a p-nitrophenyl phosphate assay. Flavonoids (3 and 4) and stilbene (5) exhibited notable inhibitory activity, with IC<sub>50</sub> values of 13.30 ± 0.71, 13.44 ± 0.84, and 8.68 ± 0.12 μM, respectively. In contrast, methoxyflavonoid rutinosides (1 and 2) and pyridine alkaloids (8−12) did not show significant inhibitory activity against PTP1B. These findings provide additional chemical insights into A. catechu and its constituents in relation to PTP1B inhibition.

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Publication Details

Journal
Natural Product Sciences
Published
2026-03-31
DOI
https://doi.org/10.20307/nps.2026.32.1.50
Primary Topic
Oral Health Pathology and Treatment
Type
article
Field-Weighted Citation Impact
0.00

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article

A New Methoxyflavonoid Rutinoside and PTP1B-Inhibitory Phenolic Compounds from the Water Extract of Areca catechu L.

Kang-Hyun Han, Sang‐Jin Park, Jungmoo Huh, Thu Hương Trần et al.
Natural Product Sciences
Oral Health Pathology and Treatment
article

A New Methoxyflavonoid Rutinoside and PTP1B-Inhibitory Phenolic Compounds from the Water Extract of Areca catechu L.

Kang-Hyun Han, Sang‐Jin Park, Jungmoo Huh, Thu Hương Trần, Seung Eui Min, Trong Trieu Tran, Jeong-Ah Kim, Manh Tuan Ha, Byung-Sun Min
article en

Abstract

Phytochemical investigation of the water extract and alkaloid fraction of Areca catechu L. led to the isolation of one new methoxyflavonoid rutinoside (1), together with eleven known compounds (2−12), five of which (8−12) belong to the pyridine alkaloid class. The structure of the new compound was elucidated through extensive spectroscopic analyses, including 1D and 2D NMR experiments and high-resolution mass spectrometry. Notably, rhamnazin-3-O-rutinoside (2) is reported here for the first time from this species. The isolated compounds were evaluated for their inhibitory activity against protein tyrosine phosphatase 1B (PTP1B) using a p-nitrophenyl phosphate assay. Flavonoids (3 and 4) and stilbene (5) exhibited notable inhibitory activity, with IC<sub>50</sub> values of 13.30 ± 0.71, 13.44 ± 0.84, and 8.68 ± 0.12 μM, respectively. In contrast, methoxyflavonoid rutinosides (1 and 2) and pyridine alkaloids (8−12) did not show significant inhibitory activity against PTP1B. These findings provide additional chemical insights into A. catechu and its constituents in relation to PTP1B inhibition.

Natural Product SciencesVol. 32(1)
Ministry of Food and Drug Safety
Clean water and sanitation
Openalex Percentile: Top 20%
Oral Health Pathology and Treatment
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A New Methoxyflavonoid Rutinoside and PTP1B-Inhibitory Phenolic Compounds from the Water Extract of Areca catechu L. — Kang-Hyun Han, Sang‐Jin Park, et al. · Natural Product Sciences (2026) | TGRS Research Map | TGRS