# N-Alkylamino Stilbene Compounds as Amyloid β Inhibitors for Alzheimer’s Disease Research

**Authors:** Citlali Gutiérrez, Liang Sun, Yiran Huang, Kai Gui, Karna Terpstra, Liviu M. Mirica

PMC · DOI: 10.3390/molecules30112471 · Molecules · 2025-06-05

## TL;DR

This paper introduces new compounds that can inhibit the formation of amyloid beta aggregates, which are linked to Alzheimer's disease.

## Contribution

The study develops N-alkylamino stilbene compounds that selectively target amyloid beta aggregates.

## Key findings

- The compounds modulate the formation of amyloid beta aggregates.
- They show selectivity toward amyloid beta species over other proteins.
- These compounds have potential for developing AD probes.

## Abstract

Alzheimer’s disease (AD) is an incurable neurodegenerative disorder that debilitates an overwhelming number of people in the aging population worldwide. The aggregated forms of the amyloid beta (Aβ) peptide play an important role in the onset of AD. Small molecules that can bind to Aβ are useful for in vitro assays, in vivo imaging, and in therapeutic research. Herein, a series of compounds that can target Aβ aggregates and inhibit their formation were developed. The interaction of several compounds with the Aβ peptide was found to modulate the formation of aggregates. These N-alkylamino stilbene compounds offer selectivity toward Aβ species against other in situ proteins and have potential for aiding the development of soluble Aβ aggregate selective AD probes.

## Linked entities

- **Diseases:** Alzheimer’s disease (MONDO:0004975)

## Full-text entities

- **Genes:** APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}
- **Diseases:** neurodegenerative disorder (MESH:D019636), AD (MESH:D000544)
- **Chemicals:** N-Alkylamino Stilbene (-)

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12156033/full.md

## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC12156033/full.md

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Source: https://tomesphere.com/paper/PMC12156033