FOXO4-DRI¶
Identification¶
| Property | Value |
|---|---|
| CAS Number | — (D-Retro-Inverso peptide) |
| Molecular Formula | — |
| Molecular Weight | ~4,316.0 Da |
| Sequence | D-Retro-Inverso 47-mer (all D-amino acids, reversed sequence) |
| Amino Acid Count | 47 (all D-amino acids, retro-inverso) |
| Appearance | White to off-white lyophilized powder |
| Purity Standard | ≥99% by HPLC |
| Solubility | Soluble in sterile water or PBS |
| Storage | 2–8°C, desiccated, protect from light |
Category: Nootropic & Anti-Aging
Catalog SKU: PSH-FOXO4-5MG
Research Background¶
FOXO4-DRI (D-Retro-Inverso) is a modified peptide that disrupts the FOXO4-p53 interaction in senescent cells — a mechanism for targeted senescent cell clearance (senolysis). It represents a fundamentally different approach from signaling peptides: rather than modulating a pathway, it targets a specific protein-protein interaction. The D-Retro-Inverso modification (all D-amino acids, reversed sequence) makes the peptide essentially invisible to proteases, conferring dramatically extended half-life. Developed by the de Keizer lab, FOXO4-DRI is a landmark tool in cellular senescence research.
Key Mechanisms¶
| Mechanism | Details |
|---|---|
| FOXO4-p53 Disruption | Competes with FOXO4 for p53 binding → releases nuclear p53 → triggers apoptosis |
| Senescent Cell Selectivity | Senescent cells have elevated FOXO4-p53 complexes — DRI selectively disrupts these |
| D-Retro-Inverso Design | All-D-amino acid, reversed sequence → complete protease resistance → extended half-life |
| BAX/BAK Activation | Released p53 → mitochondrial BAX/BAK → cytochrome c → caspase cascade → apoptosis |
Research Focus Areas¶
Cellular Senescence¶
p53-mediated senescent cell apoptosis induction
Senolytic Research¶
Selective elimination of senescent cells without affecting proliferating cells
Aging Models¶
Age-related pathology reduction; healthspan extension in rodent models
Chemotherapy Protection¶
Doxorubicin-induced senescence and cardiotoxicity mitigation
Available Configurations¶
| Configuration | Content | Best For |
|---|---|---|
| Standard Kit | 5 mg × 10 vials | Senolytic research; evaluation |
| Bulk Kit | 10 mg × 10 vials | Aging models; repeat orders |
| Custom | Custom mg × custom vials | OEM; private-label |
Tiered Wholesale Pricing¶
| Volume | Discount | For |
|---|---|---|
| 1 kit | List price | Evaluation; competitive analysis |
| 5+ kits | 10% off | Initial portfolio expansion |
| 20+ kits | 20% off | Mid-size distributors |
| 50+ kits | 30% off | Regional distributors |
Quality Specifications¶
| Parameter | Method | Criterion |
|---|---|---|
| Purity | HPLC at 214 nm, C18 column | ≥99.0% peak area |
| Identity (MW) | MALDI-TOF MS | ~4,316.0 ± 2.0 Da |
| Appearance | Visual inspection | White to off-white powder |
| Chiral Purity | Chiral amino acid analysis | All D-amino acids confirmed |
| Residual Moisture | Karl Fischer | ≤3% |
Frequently Asked Questions¶
Q1: What is FOXO4-DRI and how does it work?¶
FOXO4-DRI is a 47-amino acid D-Retro-Inverso peptide that disrupts the FOXO4-p53 interaction in senescent cells. FOXO4 normally sequesters p53 in the nucleus of senescent cells, preventing apoptosis. DRI displaces FOXO4 → releases p53 → triggers mitochondrial apoptosis cascade → selectively eliminates senescent cells.
Q2: What does D-Retro-Inverso mean?¶
The peptide is synthesized from all D-amino acids (not natural L-form) in reversed sequence order. Result: same 3D side-chain topology as natural L-peptide but completely resistant to proteolytic degradation — proteases only recognize L-amino acids.
Q3: How does FOXO4-DRI selectively target senescent cells?¶
Senescent cells accumulate high FOXO4-p53 complexes as part of their anti-apoptotic survival program. DRI specifically disrupts these. Healthy, proliferating cells have much lower complex levels and are correspondingly less affected.
Q4: What is the difference vs other senolytics?¶
Most senolytics (dasatinib, quercetin) target BCL-2 family proteins broadly. FOXO4-DRI targets a specific protein-protein interaction unique to senescent cell biology — the FOXO4-p53 nuclear complex — potentially providing greater senescent cell selectivity.
Q5: What QC is unique to FOXO4-DRI?¶
Beyond standard tests: chiral amino acid analysis confirms all D-configuration residues; MALDI-TOF MS for accurate mass of this larger 47-amino acid peptide. All in batch-specific COA.
Key Research References¶
| Reference | PMID | Key Finding |
|---|---|---|
| Baar MP et al. "Targeted apoptosis of senescent cells restores tissue homeostasis in response to chemotoxicity and aging." Cell. 2017;169(1):132–147.e16. | 28340339 | FOXO4-DRI displaces FOXO4 from p53 in senescent cells, triggering p53-mediated apoptosis; restores fitness and hair density in naturally aged and progeroid mouse models |
| de Keizer PLJ. "The Fountain of Youth by Targeting Senescent Cells?" Trends Mol Med. 2017;23(1):6–17. | 28041565 | Review of senolytic strategies including FOXO4-DRI as a targeted protein-protein interaction disruptor for senescent cell clearance |
Stability & Storage¶
| Condition | Degradation Profile |
|---|---|
| D-Retro-Inverso Stability | All D-amino acids with reversed sequence — essentially invisible to proteases. Dramatically extended half-life compared to L-peptide counterparts |
| Lyophilized Storage | Standard peptide stability; 24 months at 2–8°C in desiccated environment, protect from light |
| Neutral pH (6.0–7.5) | Stable; excellent protease resistance across a range of pH conditions due to D-amino acid backbone |
| Reconstituted Solution | 24 h at 2–8°C; aliquot and freeze at −20°C for extended use. Avoid repeated freeze-thaw |
| 47-mer Handling | Larger peptide (MW ~4,316 Da) — use siliconized vials and low-retention tips to minimize non-specific adsorption |
Source & Purchase¶
For research-grade FOXO4 DRI and related compounds in this category, visit the PeptideSourceHub category page for bulk pricing and available specifications.
Browse FOXO4 DRI & Related Products →
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