Also known as: FOXO4-D-Retro-Inverso, Senolytic peptide
FOXO4-DRI is a senolytic peptide research compound (not FDA-approved for human use) studied for senescent cell elimination (senolytics). FOXO4-DRI is a senolytic peptide that forces senescent ('zombie') cells to undergo programmed death by breaking the survival signal that keeps them alive, studied in mice for tissue rejuvenation and reversal of aging markers. Research dose: 5–10 mg pulsed — 3 days per week, per mouse study protocol. Half-life: 2 hours. Available from COA-verified vendors with code PEPTIDEX for up to 20% off.
Rankings independent · Research use only
D-retro-inverso peptide that disrupts the interaction between FOXO4 and p53 in senescent cells. In normal cells, FOXO4 retains p53 in the nucleus preventing apoptosis — a mechanism senescent cells exp
⚠️ Educational only · Not medical advice · Consult a doctor · Most peptides are research-only / not FDA-approved for human use
COA-verified vendors · Use code PEPTIDEX for up to 20% off
| Vendor | Purity | List Price | With PEPTIDEX | Code | Shop |
|---|---|---|---|---|---|
Bio Longevity LabsTriple-Tested | 99%+ | $274.97/10mg | $233.72Save 15% | PEPTIDEX | Shop |
Use code PEPTIDEX for 15% off at Bio Longevity Labs.
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FOXO4-DRI (also known as FOXO4-D-Retro-Inverso, Senolytic peptide) is a prominently researched experimental compound classified strictly within the Senolytic Peptide framework. Operating primarily through advanced pharmacological pathways, its core mechanism of action is as follows: it d-retro-inverso peptide that disrupts the interaction between FOXO4 and p53 in senescent cells. In normal cells, FOXO4 retains p53 in the nucleus preventing apoptosis — a mechanism senescent cells exploit for survival. FOXO4-DRI competitively binds FOXO4, freeing p53 to migrate to mitochondria, triggering apoptosis selectively in senescent cells. Results in clearance of senescent cell burden, reduction of the senescence-associated secretory phenotype (SASP), and tissue rejuvenation markers in aged mice. with a documented biological half-life of roughly 2 hours, In preclinical investigative trials and independent academic studies, researchers utilizing FOXO4-DRI have documented significant, quantifiable biological outcomes, primarily focusing on senescent cell elimination (senolytics), longevity, tissue rejuvenation, sasp reduction. Typical research protocols investigate administering 5000 to 10000mcg via subq pathways pulsed — 3 days per week, per mouse study protocol. However, it is critically important to understand that while FOXO4-DRI demonstrates profound physiological potential in highly controlled laboratory settings, it remains classified strictly as a research chemical and has not been approved by the United States Food and Drug Administration (FDA) for human therapeutic, diagnostic, or dietary consumption. Independent chemical analysis via rigorous third-party Certificate of Analysis (COA) testing utilizing High-Performance Liquid Chromatography (HPLC) and Mass Spectrometry (MS) remains the industry gold standard for verifying its base elemental stability when reconstituted appropriately in sterile bacteriostatic water.
D-retro-inverso peptide that disrupts the interaction between FOXO4 and p53 in senescent cells. In normal cells, FOXO4 retains p53 in the nucleus preventing apoptosis — a mechanism senescent cells exploit for survival. FOXO4-DRI competitively binds FOXO4, freeing p53 to migrate to mitochondria, triggering apoptosis selectively in senescent cells. Results in clearance of senescent cell burden, reduction of the senescence-associated secretory phenotype (SASP), and tissue rejuvenation markers in aged mice.
⚠ EXPERIMENTAL COMPOUND. NO HUMAN CLINICAL TRIALS. Mechanism is potent and irreversible (apoptosis induction). Selective for senescent cells in mouse models but human selectivity profiles are unknown. Aggressive Herxheimer-like inflammatory response from SASP release possible during senescent cell clearance. DO NOT USE without comprehensive medical supervision.
See our evidence grading methodology for how we evaluate and grade peptide safety data.
⚠️ For educational purposes only. Not medical advice. Consult a healthcare professional before using any peptide.
Mouse study: 10mg/kg IP 3x/week. No validated human protocol. Human equivalent dose extrapolation is not clinically validated.
Week 1
Senescent cell clearance begins; possible SASP-driven inflammatory response
Weeks 2–4
Tissue rejuvenation markers in mouse models (fur density, fitness scores)
| Side Effect | Incidence | Severity |
|---|---|---|
SASP inflammatory response Transient cytokine surge from dying senescent cells | Unknown in humans | moderate |
Unknown off-target apoptosis Selective for senescent cells in mouse models; human selectivity uncharacterized | Unknown | rare |
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⚠️ Educational only · Not medical advice · For research use only. Information on this page is compiled from peer-reviewed literature and is intended strictly for educational and informational purposes. Peptides discussed may be unapproved research chemicals — consult a licensed healthcare professional before considering any peptide compound. Read our full disclaimer
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