# Cochlioquinones 1968–2024: Chemistry, Biosynthesis, and Biological Activities with Future Perspectives

**Authors:** Huiqi Fang, Qi Li, Lin Chen, Gang Ding

PMC · DOI: 10.3390/jof11100712 · Journal of Fungi · 2025-09-30

## TL;DR

This review summarizes the chemistry, biosynthesis, and biological activities of cochlioquinones from 1968 to 2024, highlighting their potential in agriculture and pharmaceuticals.

## Contribution

The paper systematically compiles and categorizes the structural and functional diversity of cochlioquinones over five decades.

## Key findings

- Eighty-one cochlioquinone analogues with diverse post-modifications have been isolated from fungi.
- Cochlioquinones show biological activities like phytotoxicity, antibacterial effects, and cytotoxicity.
- The compounds are classified into benzoquinone-type and phenol-type based on their structures.

## Abstract

Cochlioquinones are a member of meroterpenoids possessing a core 6/6/6/6 tetracyclic ring system, which originate from the polyketide-terpenoid hybrid biosynthesis. Up to date, there are eighty-one analogues with diverse post-modifications isolated from different fungi, most of which exhibit different biological activities, such as phytotoxic, antibacterial, cytotoxic, and immunosuppressive effects. Structurally, cochlioquinones can be mainly categorized into two classes: benzoquinone-type and phenol-type cochlioquinones, respectively. In this review, chemistry and biology of cochlioquinones including the structures, NMR and MS features, bioactivities, and biosynthesis from 1968 to 2024 are systematically summarized, which might provide insights into the exploration and utilization of this group of meroterpenoids in the agricultural or pharmaceutical industry.

## Full-text entities

- **Diseases:** cytotoxic (MESH:D064420)
- **Chemicals:** phenol (MESH:D019800), benzoquinone (MESH:C004532), terpenoid (MESH:D013729), polyketide (MESH:D061065), Cochlioquinones (-)

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12565317/full.md

## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC12565317/full.md

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Source: https://tomesphere.com/paper/PMC12565317