GymnopeptidesC and D, Highly <i>N</i>‑MethylatedFungal Cyclopeptides

An in-depth chemical study of the fungus <i>Gymnopus fusipes</i> led to the discovery of two new cyclooctadecapeptides, gymnopeptides C and D, besides the known gymnopeptides A and B. Spectroscopic studies, as well as Marfey’s analysis, and molecular modeling studies revealed the characteristic structural features of these cyclopeptides. Gymnopeptides A–D demonstrated antiproliferative activity on the A375 human cancer cell line, induced apoptosis by upregulation of caspase-3 activity, and acted as a suppressor of cell migration.

Publication Details

Journal
Figshare
Published
2025-02-27
DOI
https://doi.org/10.1021/acs.jnatprod.4c01132.s001
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
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GymnopeptidesC and D, Highly N‑MethylatedFungal Cyclopeptides

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Microbial Natural Products and Biosynthesis
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GymnopeptidesC and D, Highly N‑MethylatedFungal Cyclopeptides

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Abstract

An in-depth chemical study of the fungus <i>Gymnopus fusipes</i> led to the discovery of two new cyclooctadecapeptides, gymnopeptides C and D, besides the known gymnopeptides A and B. Spectroscopic studies, as well as Marfey’s analysis, and molecular modeling studies revealed the characteristic structural features of these cyclopeptides. Gymnopeptides A–D demonstrated antiproliferative activity on the A375 human cancer cell line, induced apoptosis by upregulation of caspase-3 activity, and acted as a suppressor of cell migration.

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Openalex Percentile: Top 44%
Microbial Natural Products and Biosynthesis
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GymnopeptidesC and D, Highly <i>N</i>‑MethylatedFungal Cyclopeptides · Figshare (2025) | TGRS Research Map | TGRS