Fusarolides A–C, Three Pyran-Macrolide Hybrids from a Marine Derived Fungal <i>Fusarium verticillioide</i> G102 as <i>Asialoglycoprotein receptor</i> 1 Inhibitor and Phytopathogenic Fungicides

Three undescribed 20-membered macrolides, fusarolides A-C (<b>1</b>-<b>3</b>), with relatively rare pyran-macrolide structures and complex chiral centers, were isolated from a marine derived fungal <i>Fusarium verticillioide</i> G102. Their chemical structures and stereoconfigurations were well elaborated. Compound <b>1</b> promoted cholesterol efflux from Huh-7 cells in a concentration-dependent manner by inhibiting <i>Asialoglycoprotein receptor</i> 1 (ASGR1), which was identified as a new therapeutic target in hypercholesterolemia in liver. Besides, compounds <b>1</b>-<b>3</b> exhibited obvious anti-phytopathogenic fungal activities.

Authors

Institutions

Publication Details

Journal
Organic Letters
Published
2025-02-03
DOI
https://doi.org/10.1021/acs.orglett.4c04789
Citations
3
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
4.18

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Fusarolides A–C, Three Pyran-Macrolide Hybrids from a Marine Derived Fungal Fusarium verticillioide G102 as Asialoglycoprotein receptor 1 Inhibitor and Phytopathogenic Fungicides

Kemin Dong, Xiao-Ping Peng, Hong‐Xiang Lou, Gang Li et al.
3 citations
Organic Letters
Microbial Natural Products and Biosynthesis
4.18
article

Fusarolides A–C, Three Pyran-Macrolide Hybrids from a Marine Derived Fungal Fusarium verticillioide G102 as Asialoglycoprotein receptor 1 Inhibitor and Phytopathogenic Fungicides

Kemin Dong, Xiao-Ping Peng, Hong‐Xiang Lou, Gang Li, Yan Liu, Yuhan Zhang, KeWei Wang, Limei Wang
article en
3 citations

Abstract

Three undescribed 20-membered macrolides, fusarolides A-C (<b>1</b>-<b>3</b>), with relatively rare pyran-macrolide structures and complex chiral centers, were isolated from a marine derived fungal <i>Fusarium verticillioide</i> G102. Their chemical structures and stereoconfigurations were well elaborated. Compound <b>1</b> promoted cholesterol efflux from Huh-7 cells in a concentration-dependent manner by inhibiting <i>Asialoglycoprotein receptor</i> 1 (ASGR1), which was identified as a new therapeutic target in hypercholesterolemia in liver. Besides, compounds <b>1</b>-<b>3</b> exhibited obvious anti-phytopathogenic fungal activities.

Organic LettersVol. 27(8)
Qingdao University (CN), Mission Health (US), Shandong University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Shandong Province, Key Technology Research and Development Program of Shandong
Life below water
Openalex Percentile: Top 8%
Microbial Natural Products and Biosynthesis
4.18
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.