A new diphenyl ether from the cultured lichen mycobiont of <i>Graphis</i> cf. <i>handelii</i>

Lichen is well-known for its various purposes. However, understanding the chemical composition and antimicrobial characteristics of <i>Graphis</i> cf. <i>handelii</i> remains insufficient. In this study, a new compound, graphinone A (<b>1</b>), together with three known compounds, handelone (<b>2</b>), 4-<i>O</i>-methylhiascic acid (<b>3</b>), and ethyl orsellinate (<b>4</b>) were isolated and structurally elucidated. Their chemical structures were established using comprehensive spectroscopic data (1D- and 2D-NMR and HRESIMS). Compounds <b>1</b>-<b>4</b> were tested for antimicrobial activity against methicillin-resistant <i>Staphylococcus aureus</i> (MRSA) and evaluated for the alpha-glucosidase inhibition.

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Publication Details

Journal
Natural Product Research
Published
2024-09-05
DOI
https://doi.org/10.1080/14786419.2024.2398736
Citations
3
Primary Topic
Lichen and fungal ecology
Type
article
Field-Weighted Citation Impact
3.09
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article

A new diphenyl ether from the cultured lichen mycobiont of Graphis cf. handelii

Chanat Aonbangkhen, Ngoc‐Hong Nguyen, Thanh‐Hung Do, Thuc‐Huy Duong et al.
3 citations
Natural Product Research
Lichen and fungal ecology
3.09
article

A new diphenyl ether from the cultured lichen mycobiont of Graphis cf. handelii

Chanat Aonbangkhen, Ngoc‐Hong Nguyen, Thanh‐Hung Do, Thuc‐Huy Duong, Duc‐Dung Pham, Chuong Hoang Nguyen, Thi‐Minh‐Dinh Tran, Jirapast Sichaem, Thi‐Phi‐Giao Vo, Thu-Hoang-Mai Nguyen, Minh-Truong-Tho Ho
article en
3 citations

Abstract

Lichen is well-known for its various purposes. However, understanding the chemical composition and antimicrobial characteristics of <i>Graphis</i> cf. <i>handelii</i> remains insufficient. In this study, a new compound, graphinone A (<b>1</b>), together with three known compounds, handelone (<b>2</b>), 4-<i>O</i>-methylhiascic acid (<b>3</b>), and ethyl orsellinate (<b>4</b>) were isolated and structurally elucidated. Their chemical structures were established using comprehensive spectroscopic data (1D- and 2D-NMR and HRESIMS). Compounds <b>1</b>-<b>4</b> were tested for antimicrobial activity against methicillin-resistant <i>Staphylococcus aureus</i> (MRSA) and evaluated for the alpha-glucosidase inhibition.

Natural Product ResearchVol. 40(1)
Thammasat University (TH), Vietnam National University Ho Chi Minh City (VN), Ton Duc Thang University (VN), Chulalongkorn University (TH), Lampang Rajabhat University (TH), Ho Chi Minh City University of Education (VN), HUTECH University, Ho Chi Minh City University of Technology (VN)
Zero hunger
Openalex Percentile: Top 9%
Lichen and fungal ecology
3.09
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