Longevity Research

FOXO4-DRI

5358.0 g/molSynthetic D-retro-inverso peptide

FOXO4-DRI is a D-retro-inverso peptide studied in research models involving cellular senescence pathways, FOXO4-p53 interaction, apoptotic signaling, DNA damage response, cellular stress biology, and tissue aging models.

$139.00

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FOR RESEARCH USE ONLY (RUO). NOT FOR DIAGNOSTIC, MEDICAL, HUMAN, OR ANIMAL USE.

Technical Specifications

Compound Information

Molecular Profile

What is FOXO4-DRI?

Molecular FormulaC228H388N86O64
Molecular Weight5358.0g/mol
Compound ClassSynthetic D-retro-inverso peptide
↗ View on PubChem

Storage Requirements

Stability Information

Store sealedProtect from lightKeep dry
2–8°C
Long-term storageLyophilized powder, as shipped. Keep sealed and refrigerated for maximum stability. Protect from light.
Cool & dry
Short-term storageStore sealed in a cool, dry place, protected from light.

For laboratory research use only. Not for human or veterinary use. Chemical data sourced from PubChem.

Peer-Reviewed Literature

The research behind this compound, cited in full.

Every reference below is a published, peer-reviewed record, linked to its PubMed entry. Provided for educational reference only, not product claims. For laboratory research use only.

  1. 01 Communications biology · 2025 FOXO4-DRI induces keloid senescent fibroblast apoptosis by promoting nuclear exclusion of upregulated p53-serine 15 phosphorylation Kong YX, et al.
  2. 02 Nature communications · 2025 The disordered p53 transactivation domain is the target of FOXO4 and the senolytic compound FOXO4-DRI Bourgeois B, et al.
  3. 03 Frontiers in bioengineering and biotechnology · 2025 FOXO4-DRI regulates endothelial cell senescence via the P53 signaling pathway Hu Z, et al.
  4. 04 Experimental gerontology · 2024 FOXO4-DRI improves spermatogenesis in aged mice through reducing senescence-associated secretory phenotype secretion from Leydig cells Li Y, et al.
  5. 05 Aging · 2020 FOXO4-DRI alleviates age-related testosterone secretion insufficiency by targeting senescent Leydig cells in aged mice Zhang C, et al.