A new lupane glycoside isolated from <i>Dendrobium officinale</i> with <i>α</i>‐glucosidase inhibitory activity

Abstract A new lupane triterpene glycoside ( 1 ) and four known compounds ( 2 ‐ 5 ) were isolated from the aerial parts of Dendrobium officinale . Their chemical structures were determined to be 3‐ O ‐ α ‐L‐arabinopyranosylbetulinic acid 28‐ O ‐ β ‐D‐glucopyranosyl‐(1→6)‐ β ‐D‐glucopyranosyl ester ( 1 ), 3‐ O ‐ α ‐L‐arabinopyranosylbetulinic acid 28‐ O ‐ α ‐L‐rhamnopyranosyl‐(1→4)‐ β ‐D‐glucopyranosyl‐(1→6)‐ β ‐ D‐glucopyranosyl ester ( 2 ), 3‐ O ‐ β ‐D‐glucopyranosylbetulinic acid 28‐ O ‐ α ‐L‐rhamnopyranosyl‐(1→4)‐ β ‐D‐glucopyranosyl‐(1→6)‐ β ‐D‐glucopyranosyl ester ( 3 ), 6α‐hydroxylup‐20(29)‐en‐3‐on 28‐oic acid ( 4 ), and lupeol ( 5 ) by analyzing the HR‐ESI‐MS, 1D and 2D NMR spectra including COSY and NOESY. Compounds 1 , 2 and 4 showed weak α‐glucosidase inhibitory activity with IC 50 values ranging from 87.5 to 98.2 µM.

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Publication Details

Journal
Vietnam Journal of Chemistry
Published
2025-04-21
DOI
https://doi.org/10.1002/vjch.70020
Primary Topic
Phytochemistry and Biological Activities
Type
article
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article

A new lupane glycoside isolated from Dendrobium officinale with α‐glucosidase inhibitory activity

Ngo Anh Bang, Phan Văn Kiệm, Bùi Hữu Tài, Đỗ Thị Trang et al.
Vietnam Journal of Chemistry
Phytochemistry and Biological Activities
article

A new lupane glycoside isolated from Dendrobium officinale with α‐glucosidase inhibitory activity

Ngo Anh Bang, Phan Văn Kiệm, Bùi Hữu Tài, Đỗ Thị Trang, Doan Thi Thu Tra, Dương Thị Dung, Dương Thị Hải Yến, Nguyễn Huy Hoàng, Nguyêñ Viêt Dũng, Phạm Hải Yến, Đan Thị Thúy Hằng, Phan Thị Thanh Hương
article en

Abstract

Abstract A new lupane triterpene glycoside ( 1 ) and four known compounds ( 2 ‐ 5 ) were isolated from the aerial parts of Dendrobium officinale . Their chemical structures were determined to be 3‐ O ‐ α ‐L‐arabinopyranosylbetulinic acid 28‐ O ‐ β ‐D‐glucopyranosyl‐(1→6)‐ β ‐D‐glucopyranosyl ester ( 1 ), 3‐ O ‐ α ‐L‐arabinopyranosylbetulinic acid 28‐ O ‐ α ‐L‐rhamnopyranosyl‐(1→4)‐ β ‐D‐glucopyranosyl‐(1→6)‐ β ‐ D‐glucopyranosyl ester ( 2 ), 3‐ O ‐ β ‐D‐glucopyranosylbetulinic acid 28‐ O ‐ α ‐L‐rhamnopyranosyl‐(1→4)‐ β ‐D‐glucopyranosyl‐(1→6)‐ β ‐D‐glucopyranosyl ester ( 3 ), 6α‐hydroxylup‐20(29)‐en‐3‐on 28‐oic acid ( 4 ), and lupeol ( 5 ) by analyzing the HR‐ESI‐MS, 1D and 2D NMR spectra including COSY and NOESY. Compounds 1 , 2 and 4 showed weak α‐glucosidase inhibitory activity with IC 50 values ranging from 87.5 to 98.2 µM.

Vietnam Journal of ChemistryVol. 63(5)
Vietnam Academy of Science and Technology (VN)
Openalex Percentile: Top 94%
Phytochemistry and Biological Activities
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