# The Chemistry and Pharmacology of the Alkaloid Barettin and Its Analogues from the Marine Sponge Geodia barretti: Progress and Perspectives

**Authors:** Christian Bailly

PMC · DOI: 10.3390/md24030110 · 2026-03-13

## TL;DR

This paper reviews the chemistry and biological roles of alkaloids from the marine sponge Geodia barretti, focusing on their potential pharmacological uses.

## Contribution

The paper provides a comprehensive review of the chemical structures, biological functions, and pharmacological properties of barettin and its analogues.

## Key findings

- Barettin and its analogues play roles in sponge stability, microbial regulation, and defense against aggressions.
- The alkaloids exhibit antioxidant and anti-inflammatory properties, making them promising for pharmacological applications.
- Synthetic methods for producing these compounds have been developed, aiding future research and drug development.

## Abstract

The cold-water siliceous sponge Geodia barretti, largely present in the North Atlantic Ocean, notably around Scandinavian costs, plays important roles in carbon and silicon cycling in the deep-sea. The demosponge provides a reservoir for numerous microorganisms. Bioactive natural products have been isolated from this sponge, in particular the indole alkaloid barettin discovered forty years ago. Barettin and analogues, notably 8,9-dihydrobarettin, 8,9-dihydro-8-hydroxybarrettin, bromobenzisoxalone barettin, and geobarrettins A-B, contribute to the maintenance of the sponge stability and security (anti-fouling) and the regulation of its microbial environment. The four indole alkaloids 6-bromo-8-hydroxyconicamin, 6-bromoconicamin, and geobarrettin C-D are also implicated in the defense of the sponge against physical and biochemical aggressions. Altogether, these ten natural products are essential to the sponge life. The present review presents a survey of the chemistry and biology associated with Geodia barretti. The pharmacological properties of (dihydro)barettin, notably their antioxidant and anti-inflammatory properties, are discussed, as well as the synthetic processes set up to produce these diketopiperazine derivatives. Their molecular targets and mechanism of action are also discussed. The review takes the sponge G. barretti from the depths of knowledge and brings barettin and analogues to the surface, with the hope of guiding future research in this field.

## Linked entities

- **Chemicals:** barettin (PubChem CID 11177588)
- **Species:** Geodia barretti (taxon 519541)

## Full-text entities

- **Genes:** TMPRSS2 (transmembrane serine protease 2) [NCBI Gene 7113] {aka PRSS10}, CTSL (cathepsin L) [NCBI Gene 1514] {aka CATL, CTSL1, MEP}, Htr2c (5-hydroxytryptamine (serotonin) receptor 2C) [NCBI Gene 15560] {aka 5-HT-1C, 5-HT-2C, 5-HT1C, 5-HT2C, 5-HT2cR, 5-HTR2C}, Htr2a (5-hydroxytryptamine (serotonin) receptor 2A) [NCBI Gene 15558] {aka 5-HT-2, 5-HT-2A, E030013E04, Htr-2, Htr2}, BCHE (butyrylcholinesterase) [NCBI Gene 590] {aka BCHED, CHE1, CHE2, E1}, CHRNA4 (cholinergic receptor nicotinic alpha 4 subunit) [NCBI Gene 1137] {aka BFNC, EBN, EBN1, NACHR, NACHRA4, NACRA4}, SIK2 (salt inducible kinase 2) [NCBI Gene 23235] {aka LOH11CR1I, QIK, SIK-2, SNF1LK2}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, HTR2C (5-hydroxytryptamine receptor 2C) [NCBI Gene 3358] {aka 5-HT1C, 5-HT2C, 5-HTR2C, 5HTR2C, HTR1C}, CXCR4 (C-X-C motif chemokine receptor 4) [NCBI Gene 7852] {aka CD184, D2S201E, FB22, HM89, HSY3RR, LCR1}, HTR2A (5-hydroxytryptamine receptor 2A) [NCBI Gene 3356] {aka 5-HT2A, HTR2}, ITGAV (integrin subunit alpha V) [NCBI Gene 3685] {aka CD51, IDNDC, MSK8, VNRA, VTNR}, CAMK1 (calcium/calmodulin dependent protein kinase I) [NCBI Gene 8536] {aka CAMKI}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, ACHE (acetylcholinesterase (Yt blood group)) [NCBI Gene 43] {aka ACEE, ARACHE, N-ACHE, YT}, RIPK2 (receptor interacting serine/threonine kinase 2) [NCBI Gene 8767] {aka CARD3, CARDIAK, CCK, GIG30, RICK, RIP2}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}
- **Diseases:** neurodegenerative, cardiovascular, pulmonary, and musculoskeletal metabolic diseases (MESH:D019636), neuropathic pain (MESH:D009437), injury to (MESH:D014947), COVID-19 (MESH:D000086382), inflammatory (MESH:D007249), infectious (MESH:D003141), necrosis (MESH:D009336), cancers (MESH:D009369), myocardial infarction (MESH:D009203)
- **Chemicals:** EDTA (MESH:D004492), piperazinedione (MESH:C003905), LiHMDS (MESH:C442341), DMP (MESH:D014494), amide (MESH:D000577), shikimic acid (MESH:D012765), phidianidine A (MESH:C559224), Boc2O (MESH:C027600), 6-BHP (MESH:C014372), tryptophan (MESH:D014364), 16d (MESH:C032363), guanidine (MESH:D019791), lipid (MESH:D008055), 2,5-diketopiperazine (MESH:C010939), alcohol (MESH:D000438), dipodazine (MESH:C514604), oxazolidinone (MESH:D023303), Fe (MESH:D007501), rhodanine (MESH:D012236), 6-bromoindole (MESH:C575316), arginine (MESH:D001120), brevianamide F. (MESH:C000590722), EtOH (MESH:D000431), terpenes (MESH:D013729), Barettin (MESH:C484472), fatty acids (MESH:D005227), C (MESH:D002244), acetone (MESH:D000096), galanthamine (MESH:D005702), amidine (MESH:D000578), cpd (MESH:C007077), disulfide (MESH:D004220), indole-3-carboxaldehyde (MESH:C012381), lactam (MESH:D007769), acid (MESH:D000143), dipeptide (MESH:D004151), purine (MESH:C030985), TFA (MESH:D014269), indole alkaloid (MESH:D026121), pyridine (MESH:C023666), bromine (MESH:D001966), aldehyde (MESH:D000447), Benzo[g]dipodazine (-), dioxane (MESH:C025223), N-methylmorpholine (MESH:C038816), 1,8-diaza-7-bicyclo[5.4.0]undecene (MESH:C031033), hydantoin (MESH:D006827), H2O (MESH:D014867), THF (MESH:C018674), bentonite (MESH:D001546), Cu (MESH:D003300), ketanserin (MESH:D007650), HOBt (MESH:C011852), guanine (MESH:D006147), N (MESH:D009584), barrettide A (MESH:C000602711), indole (MESH:C030374), formamide (MESH:C031066), alkaloid (MESH:D000470), 6-bromotryptophan (MESH:C110059)
- **Species:** Geodia (genus) [taxon 6046], Cucumaria miniata (red sea cucumber, species) [taxon 28833], Apostichopus japonicus (Japanese sea cucumber, species) [taxon 307972], Porifera (sponges, phylum) [taxon 6040], Homo sapiens (human, species) [taxon 9606], Meloidogyne incognita (southern root-knot nematode, species) [taxon 6306], Tobacco mosaic virus (no rank) [taxon 12242], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Geodia hentscheli (species) [taxon 664260], Pachymatisma johnstonia (species) [taxon 77183], Mytilus edulis (blue mussel, species) [taxon 6550], Ammonia (genus) [taxon 29189], Mus musculus (house mouse, species) [taxon 10090], PX clade (clade) [taxon 569578], Foraminifera (foraminifers, phylum) [taxon 29178], Cicer arietinum (chickpea, species) [taxon 3827], Geodia barretti (species) [taxon 519541], Gigantometra gigas (species) [taxon 95701], Aspergillus versicolor (species) [taxon 46472], Geodia macandrewii (species) [taxon 519544], Amphibalanus improvisus (species) [taxon 1220549], Aspergillus sp. (species) [taxon 5065], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Gammacoronavirus (genus) [taxon 694013]
- **Cell lines:** HepG2 — Homo sapiens (Human), Hepatoblastoma, Cancer cell line (CVCL_0027), THP-1 — Homo sapiens (Human), Childhood acute monocytic leukemia, Cancer cell line (CVCL_0006)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13027785/full.md

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Source: https://tomesphere.com/paper/PMC13027785