Erinacenones M–Y, Part 2: Thirteen New Isoindolinone Alkaloids with α-Glucosidase Inhibitory Activity from Liquid Cultures of the Edible and Medicinal Mushroom Hericium erinaceus

As a continuation of our previous study on erinacenones A–L (Part 1), thirteen previously undescribed isoindolin-1-ones, erinacenones M–Y (1–13), were isolated from the fermentation broth of Hericium erinaceus. Their structures were elucidated by extensive spectroscopic analyses (1D and 2D NMR, HRESIMS), and the absolute configurations of 1–13 were determined by comparing their specific rotations with those of related phthalimidines (14–23). Compound 11 showed the highest α-glucosidase inhibitory activity among the tested compounds, with 31.5% inhibition at 50 μM. These findings significantly enrich the chemical diversity of isoindolinone metabolites from H. erinaceus and provide a foundation for future structure–activity relationship studies.

Authors

Institutions

Publication Details

Journal
Molecules
Published
2026-09-20
DOI
https://doi.org/10.3390/molecules31183333
Primary Topic
Fungal Biology and Applications
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
article

Erinacenones M–Y, Part 2: Thirteen New Isoindolinone Alkaloids with α-Glucosidase Inhibitory Activity from Liquid Cultures of the Edible and Medicinal Mushroom Hericium erinaceus

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

Erinacenones M–Y, Part 2: Thirteen New Isoindolinone Alkaloids with α-Glucosidase Inhibitory Activity from Liquid Cultures of the Edible and Medicinal Mushroom Hericium erinaceus

Ji‐Kai Liu, Lin-Lin Yuan
article en

Abstract

As a continuation of our previous study on erinacenones A–L (Part 1), thirteen previously undescribed isoindolin-1-ones, erinacenones M–Y (1–13), were isolated from the fermentation broth of Hericium erinaceus. Their structures were elucidated by extensive spectroscopic analyses (1D and 2D NMR, HRESIMS), and the absolute configurations of 1–13 were determined by comparing their specific rotations with those of related phthalimidines (14–23). Compound 11 showed the highest α-glucosidase inhibitory activity among the tested compounds, with 31.5% inhibition at 50 μM. These findings significantly enrich the chemical diversity of isoindolinone metabolites from H. erinaceus and provide a foundation for future structure–activity relationship studies.

MoleculesVol. 31(18)
Anhui University of Traditional Chinese Medicine (CN), Tarim University (CN)
Openalex Percentile: Top 12%
Fungal Biology and Applications
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Erinacenones M–Y, Part 2: Thirteen New Isoindolinone Alkaloids with α-Glucosidase Inhibitory Activity from Liquid Cultures of the Edible and Medicinal Mushroom Hericium erinaceus — Ji‐Kai Liu, Lin-Lin Yuan · Molecules (2026) | TGRS Research Map | TGRS