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Description

Binding energy calculations and interaction maps for curcumin versus RuCurcumin with amyloid-beta 1-40 and 1-42 peptides, highlighting improved binding affinity of the ruthenium derivative.

Figure 2

Diagram

Source Paper

Enhancing the Amyloid-β Anti-Aggregation Properties of Curcumin via Arene-Ruthenium(II) Derivatization.

International journal of molecular sciences (2022)

PMID: 35955845

DOI: 10.3390/ijms23158710

Cite This Figure

![Figure 2: Binding energy calculations and interaction maps for curcumin versus RuCurcumin with amyloid-beta 1-40 and 1-42 peptides, highlighting improved binding affinity of the ruthenium derivative.]()

> Source: Massimiliano Cuccioloni et al. "Enhancing the Amyloid-β Anti-Aggregation Properties of Curcumin via Arene-Ruthen." *International journal of molecular sciences*, 2022. PMID: [35955845](https://pubmed.ncbi.nlm.nih.gov/35955845/)
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  <img src="" alt="Binding energy calculations and interaction maps for curcumin versus RuCurcumin with amyloid-beta 1-40 and 1-42 peptides, highlighting improved binding affinity of the ruthenium derivative." />
  <figcaption>Figure 2. Binding energy calculations and interaction maps for curcumin versus RuCurcumin with amyloid-beta 1-40 and 1-42 peptides, highlighting improved binding affinity of the ruthenium derivative.<br>  Source: Massimiliano Cuccioloni et al. "Enhancing the Amyloid-β Anti-Aggregation Properties of Curcumin via Arene-Ruthen." <em>International journal of molecular sciences</em>, 2022. PMID: <a href="https://pubmed.ncbi.nlm.nih.gov/35955845/">35955845</a></figcaption>
</figure>