# Modified Flavonoids with Diamines and Polyamines Provide Enhanced Fluorescence and Antimicrobial Activity

**Authors:** Sevasti Matsia, Athanasios Salifoglou

PMC · DOI: 10.3390/ijms27010253 · International Journal of Molecular Sciences · 2025-12-25

## TL;DR

Scientists created new flavonoid compounds with amines that glow more brightly and fight bacteria, especially E. coli.

## Contribution

The study introduces novel flavonoid-(poly)amine derivatives with enhanced fluorescence and selective antimicrobial activity.

## Key findings

- Naringin-based derivatives showed enhanced fluorescence compared to others.
- Modified flavonoids selectively inhibited E. coli, a Gram-negative bacterium.
- Chemical modifications significantly affected photoluminescence and antimicrobial properties.

## Abstract

Development of new biologically active materials based on natural products has, over the years, attracted considerable attention due to their effectiveness in human health and disease. Polyphenolic compounds, particularly flavonoids, provide a wide range of health benefits, including antioxidant, anti-inflammatory, anticancer, and antibacterial properties. A series of novel Schiff base derivatives of flavonoids with amino-containing linkers was successfully designed and synthesized through condensation reactions. Naringin and naringenin derivatives with diamines, including ethylenediamine (EDA), 1,3-diamino-2-propanol (DA-2-PrOH), tetramethylenediamine (TMEDA), pentamethylenediamine (PMEDA), as well as polyamines spermidine (SPD) and spermine (SPM), were synthesized and well-characterized through FT-IR, UV–Visible, ESI–MS, 1H and 13C NMR spectroscopy, and elemental analysis. The so confirmed and well-characterized derivatives were subjected to photoluminescence studies, exhibiting enhanced activity, especially for naringin-based derivatives, and quenching in some others, thus verifying the significance of chemically modifying the conjugated systems of these molecules. Their biological activity was examined in the case of their antimicrobial efficacy against two Gram (+) (Staphylococcus aureus and Bacillus cereus) and two Gram (−) (Escherichia coli and Xanthomonas campestris) bacterial strains. Antibacterial screening projected selectivity of modified flavonoids against E. coli, proposing new “dense” flavonoid-(poly)amine materials as multifunctional antimicrobial agents and fluorescent probes.

## Linked entities

- **Chemicals:** naringin (PubChem CID 442428), naringenin (PubChem CID 932), ethylenediamine (PubChem CID 3301), 1,3-diamino-2-propanol (PubChem CID 61157), tetramethylenediamine (PubChem CID 1045), pentamethylenediamine (PubChem CID 273), spermidine (PubChem CID 1102), spermine (PubChem CID 1103)
- **Species:** Staphylococcus aureus (taxon 1280), Bacillus cereus (taxon 1396), Escherichia coli (taxon 562), Xanthomonas campestris (taxon 339)

## Full-text entities

- **Diseases:** inflammatory (MESH:D007249)
- **Chemicals:** TMEDA (MESH:D011700), SPD (MESH:D013095), 1H (-), PMEDA (MESH:D002103), Schiff base (MESH:D012545), 13C (MESH:C000615229), EDA (MESH:C031234), SPM (MESH:D013096), 1,3-diamino-2-propanol (MESH:C017203), Diamines (MESH:D003959), Polyamines (MESH:D011073), Naringin (MESH:C005274), naringenin (MESH:C005273), Flavonoids (MESH:D005419)
- **Species:** Bacillus cereus (species) [taxon 1396], Homo sapiens (human, species) [taxon 9606], Escherichia coli (E. coli, species) [taxon 562], Staphylococcus aureus (species) [taxon 1280], Xanthomonas campestris (species) [taxon 339]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12785322/full.md

## References

66 references — full list in the complete paper: https://tomesphere.com/paper/PMC12785322/full.md

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Source: https://tomesphere.com/paper/PMC12785322