# In Vitro and In Silico Evaluation of the Anti-Aging Potential of Eugenia uniflora UAE Extracts

**Authors:** Desy Muliana Wenas, Berna Elya, Sutriyo Sutriyo, Heri Setiawan, Rozana Othman, Syamsu Nur, Nita Triadisti, Fenny Yunita, Erwi Putri Setyaningsih

PMC · DOI: 10.3390/molecules30153168 · 2025-07-29

## TL;DR

This study explores the anti-aging potential of extracts from the Eugenia uniflora plant, finding that seed extracts show strong antioxidant and enzyme-inhibiting properties.

## Contribution

The study introduces the anti-elastase and antioxidant potential of Eugenia uniflora seed extracts as a novel natural candidate for anti-aging products.

## Key findings

- E. uniflora seed extract showed the highest antioxidant activity with an IC50 of 5.23 µg/mL.
- The extract exhibited significant anti-elastase activity with an IC50 of 114.14 µg/mL.
- Molecular docking predicted several compounds as strong pancreatic elastase inhibitors.

## Abstract

Skin aging is a natural biological process that can be accelerated by free radical induction, leading to a reduction in skin elasticity and the formation of wrinkles due to the depletion of elastin. Eugenia uniflora (dewandaru) is a promising plant believed to possess anti-aging properties, primarily attributed to its major constituents, myricitrin and quercetin. This study aimed to investigate the anti-elastase and antioxidant properties of Eugenia uniflora stem bark, ripe fruit, and seed extracts. Extracts were obtained using an ultrasound-assisted extraction (UAE) method with 70% ethanol. Quantitative phytochemical analysis involved measuring the total phenolic content (TPC), total flavonoid content (TFC), and antioxidant activity. Bioactive constituents were identified using LC-MS analysis, and their interactions with target enzymes were further evaluated through in silico molecular docking. The results demonstrated that the E. uniflora seed extract exhibited the highest antioxidant activity, with an IC50 of 5.23 µg/mL (DPPH assay) and a FRAP value of 3233.32 µmol FeSO4/g. Furthermore, the ethanolic seed extract showed significant anti-elastase activity with an IC50 of 114.14 µg/mL. Molecular docking predicted strong potential for several compounds as pancreatic elastase inhibitors, including 5-phenylvaleric acid, 2-(3-phenylpropyl)phenol, n-amylbenzene, 2-aminoadipic acid, and traumatin, each showing a prediction activity (PA) value exceeding 0.6. Notably, these compounds also exhibited inhibitory activity against tyrosinase. These findings collectively underscore the significant promise of E. uniflora seed extract as a novel and natural candidate for pharmacocosmeceutical product development, particularly for anti-aging applications.

## Linked entities

- **Chemicals:** myricitrin (PubChem CID 5281673), quercetin (PubChem CID 5280343), 5-phenylvaleric acid (PubChem CID 16757), 2-(3-phenylpropyl)phenol (PubChem CID 572468), n-amylbenzene (PubChem CID 10864), 2-aminoadipic acid (PubChem CID 469), traumatin (PubChem CID 5312889)
- **Species:** Eugenia uniflora (taxon 119951)

## Full-text entities

- **Chemicals:** flavonoid (MESH:D005419), myricitrin (MESH:C008577), 2-aminoadipic acid (MESH:D015074), ethanol (MESH:D000431), quercetin (MESH:D011794), DPPH (MESH:C004931), traumatin (MESH:C092125), 5-phenylvaleric acid (MESH:C400347), 2-(3-phenylpropyl)phenol (-)
- **Species:** Eugenia uniflora (Brazil-cherry, species) [taxon 119951]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12348075/full.md

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Source: https://tomesphere.com/paper/PMC12348075