Erinacenones A–L: Twelve New Isoindolinone Alkaloids from the Edible and Medicinal Mushroom Hericium erinaceus

A total of twelve previously unreported isoindolin-1-one compounds, erinacenones A-L (<b>1</b>-<b>12</b>), were isolated from liquid cultures of the medicinal fungus <i>Hericium erinaceus</i>. Their structures were elucidated based on spectroscopic data analysis. The absolute configuration of <b>12</b> was determined by comparing its optical rotations with values reported in the literature. The most distinctive feature of these compounds is that their nitrogen atoms are connected to different parts of the special structure moieties. Among them, compounds <b>3</b> and <b>4</b>, as well as <b>10</b> and <b>11</b>, are two pairs of isomers differing only by a small change in the position of one double bond. Compounds <b>4</b> and <b>5</b> were found to show cytotoxic activities, with IC<sub>50</sub> values of 24.7 and 18.4 μM, respectively, against MCF-7 cell lines.

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Publication Details

Journal
Molecules
Published
2024-10-16
DOI
https://doi.org/10.3390/molecules29204901
Citations
2
Primary Topic
Fungal Biology and Applications
Type
article
Field-Weighted Citation Impact
0.90

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article

Erinacenones A–L: Twelve New Isoindolinone Alkaloids from the Edible and Medicinal Mushroom Hericium erinaceus

Ji‐Kai Liu, Lin-Lin Yuan
2 citations
Molecules
Fungal Biology and Applications
0.90
article

Erinacenones A–L: Twelve New Isoindolinone Alkaloids from the Edible and Medicinal Mushroom Hericium erinaceus

Ji‐Kai Liu, Lin-Lin Yuan
article en
2 citations

Abstract

A total of twelve previously unreported isoindolin-1-one compounds, erinacenones A-L (<b>1</b>-<b>12</b>), were isolated from liquid cultures of the medicinal fungus <i>Hericium erinaceus</i>. Their structures were elucidated based on spectroscopic data analysis. The absolute configuration of <b>12</b> was determined by comparing its optical rotations with values reported in the literature. The most distinctive feature of these compounds is that their nitrogen atoms are connected to different parts of the special structure moieties. Among them, compounds <b>3</b> and <b>4</b>, as well as <b>10</b> and <b>11</b>, are two pairs of isomers differing only by a small change in the position of one double bond. Compounds <b>4</b> and <b>5</b> were found to show cytotoxic activities, with IC<sub>50</sub> values of 24.7 and 18.4 μM, respectively, against MCF-7 cell lines.

MoleculesVol. 29(20)
Anhui University of Traditional Chinese Medicine (CN)
National Natural Science Foundation of China
Zero hunger
Openalex Percentile: Top 23%
Fungal Biology and Applications
0.90
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Erinacenones A–L: Twelve New Isoindolinone Alkaloids from the Edible and Medicinal Mushroom Hericium erinaceus — Ji‐Kai Liu, Lin-Lin Yuan · Molecules (2024) | TGRS Research Map | TGRS