Structure–Activity Relationships of Anabaenopeptins as Carboxypeptidase and Phosphatase Inhibitors

Anabaenopeptins are a family of cyanobacterial cyclic peptides that display potent enzyme inhibition, particularly against carboxypeptidases A and B, as well as the serine/threonine phosphatases PP1 and PP2A. Defined by a 19-membered macrocyclic ring and a ureido-linked exocyclic amino acid, these compounds vary considerably in their amino acid composition, influencing both potency and selectivity. This review compiles published IC<sub>50</sub> values for natural and synthetic anabaenopeptins, organizing them by enzyme target, and highlighting recurring structural motifs that drive inhibitory activity. Through this comparative analysis, we identify emerging trends in structure-activity relationships and underscore gaps in assay standardization and structural validation. These insights provide a critical foundation for advancing the biological evaluation of anabaenopeptins as environmental contaminants, mechanistic probes, and candidate scaffolds for therapeutic development.

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Publication Details

Journal
ACS Chemical Biology
Published
2026-01-21
DOI
https://doi.org/10.1021/acschembio.5c00791
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
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article

Structure–Activity Relationships of Anabaenopeptins as Carboxypeptidase and Phosphatase Inhibitors

Jeremy J. Kodanko, Judy A. Westrick, Megan L. Quandt
ACS Chemical Biology
Microbial Natural Products and Biosynthesis
article

Structure–Activity Relationships of Anabaenopeptins as Carboxypeptidase and Phosphatase Inhibitors

Jeremy J. Kodanko, Judy A. Westrick, Megan L. Quandt
article en

Abstract

Anabaenopeptins are a family of cyanobacterial cyclic peptides that display potent enzyme inhibition, particularly against carboxypeptidases A and B, as well as the serine/threonine phosphatases PP1 and PP2A. Defined by a 19-membered macrocyclic ring and a ureido-linked exocyclic amino acid, these compounds vary considerably in their amino acid composition, influencing both potency and selectivity. This review compiles published IC<sub>50</sub> values for natural and synthetic anabaenopeptins, organizing them by enzyme target, and highlighting recurring structural motifs that drive inhibitory activity. Through this comparative analysis, we identify emerging trends in structure-activity relationships and underscore gaps in assay standardization and structural validation. These insights provide a critical foundation for advancing the biological evaluation of anabaenopeptins as environmental contaminants, mechanistic probes, and candidate scaffolds for therapeutic development.

ACS Chemical BiologyVol. 21(2)
Wayne State University (US)
Openalex Percentile: Top 81%
Microbial Natural Products and Biosynthesis
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