Vesugen
Also known as: Lys-Glu-Asp, KED
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Vesugen from $124/kit
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Key Facts: Vesugen
- Category
- Bioregulators
- FDA Status
- Not FDA Approved
- Clinical Status
- Preclinical research, approved in Russia as supplement
- Administration
- Oral capsules or sublingual
- Typical Dose
- 10-20 mg daily
- Frequency
- Once or twice daily
- Duration
- 10-30 day cycles
Mechanism of Action
Vesugen is a cytogen-class short peptide. The Khavinson group proposes that KED acts at the epigenetic level, interacting with gene promoter regions to normalize expression of vascular and neuroplasticity-related genes (such as CASP3, APOE, GAP43 and SOD2), rather than through receptor signaling. This gene-regulation model is the group's hypothesis, supported by their in-vitro and molecular-docking work, not independently established consensus.
Research Summary
The strongest published data are animal. In a 5xFAD transgenic Alzheimer's mouse model, KED restored mushroom dendritic spine density toward control levels (dosed at 400 micrograms per kg intraperitoneally), with supporting hippocampal cell-culture work. The vascular effects Vesugen is marketed for are described mainly in Russian in-vitro and observational reports and are not confirmed in registered human trials. Treat vascular efficacy claims as preliminary.
Dosing Information
Note: Animal study doses may not translate directly to humans.
Typical Dosingⓘ
Community experience
10-20 mg daily
10-20 mg daily
Once or twice daily
Vascular bioregulator. Part of Khavinson peptide system for cardiovascular support.
Research Dosingⓘ
Scientific studies
Doses from bioregulator supplement protocols
Doses from Studies
10-20 mg daily
Duration
10-30 day cycles
Administration
Oral capsules or sublingual
Timing & Administration
Best Time to Take
Morning on empty stomach
Once or twice daily
Food Recommendation
Take on empty stomach
Why This Timing?
Peptide bioregulators typically taken fasted for optimal absorption
Possible Side Effects
Not everyone experiences these effects. Individual responses vary based on dosage, duration, and personal factors.
- ●Generally well-tolerated
- ●Limited safety data outside Russia
- ●Not FDA approved
References
Research This Peptide Further
Buy in shop
Vesugen from $124/kit
1 verified vendor, ≥99% purity, COAs included.
Frequently Asked Questions
What does Vesugen do?
Vesugen is a synthetic tripeptide (Lys-Glu-Asp, or KED) from the Khavinson family of short peptide bioregulators, studied for vascular and neuroprotective effects. It is a research compound, not an approved drug, with no registered human clinical trials.
How does Vesugen work?
Vesugen is a cytogen-class short peptide. The Khavinson group proposes that KED acts at the epigenetic level, interacting with gene promoter regions to normalize expression of vascular and neuroplasticity-related genes (such as CASP3, APOE, GAP43 and SOD2), rather than through receptor signaling. This gene-regulation model is the group's hypothesis, supported by their in-vitro and molecular-docking work, not independently established consensus.
Is Vesugen FDA approved?
No, Vesugen is not currently FDA approved. Current status: Preclinical research, approved in Russia as supplement
What are the side effects of Vesugen?
Reported side effects include: Generally well-tolerated, Limited safety data outside Russia, Not FDA approved. Individual responses vary based on dosage, duration, and personal health factors.
What is the typical dose of Vesugen?
Community-reported common dose: 10-20 mg daily (Once or twice daily). Range: 10-20 mg daily. Administration: Oral capsules or sublingual. Community-reported doses. Not medical advice. Consult healthcare provider.
Related Peptides
Peptides commonly compared with Vesugen or used in similar applications.
Livagen
PreclinicalLivagen is a synthetic tetrapeptide (Lys-Glu-Asp-Ala, or KEDA) from the family of short "peptide bioregulators" developed by Vladimir Khavinson's group in St. Petersburg, marketed in connection with liver and immune function. The proposed appeal is epigenetic: it has been reported to loosen tightly packed chromatin in aged cells, supposedly switching age-silenced genes back on. Evidence is limited to small laboratory and cell studies, mostly from one research group, with no clinical trials, so claims should be read with heavy skepticism.
BioregulatorsOvagen
PreclinicalOvagen is a synthetic ultra-short peptide, marketed as the tripeptide Glu-Asp-Leu (EDL), and grouped with the Khavinson-style "peptide bioregulators" promoted for liver and gastrointestinal support. Like its cousins in that family, it is claimed to act at the gene-expression level in a tissue-specific way. The honest picture: there is very little verifiable scientific data on Ovagen specifically, no clinical trials, and most of what is written about it comes from vendors rather than peer-reviewed research.
BioregulatorsCortagen
PreclinicalCortagen is a synthetic tetrapeptide (Ala-Glu-Asp-Pro, AEDP) from Vladimir Khavinson's Russian peptide bioregulator program, designed as the defined-sequence stand-in for Cortexin, an older cattle brain cortex extract used in Russian neurology. It is studied mostly for nerve repair, brain function and aging, and it is not approved by the FDA or EMA. Real evidence is limited to animal experiments and Russian-institute work, with no Western randomized human trials.
BioregulatorsChonluten
PreclinicalChonluten is a synthetic tripeptide (Glu-Asp-Gly, EDG) from the Khavinson bioregulator family, pitched as the lung and bronchial peptide, derived conceptually from the same program that produced Epitalon and Cortagen. It is researched for respiratory tissue and age-related lung decline, and it has no FDA or EMA approval. The evidence is essentially all preclinical or uncontrolled Russian clinical observation, with no randomized human trials.
BioregulatorsCrystagen
PreclinicalCrystagen is a synthetic tripeptide (Glu-Asp-Pro, or EDP) from the Khavinson family of short peptide bioregulators, studied as an immune and thymic regulator. It is a research compound, not an approved drug, with no registered human clinical trials. Note: many vendor pages list the wrong sequence; the correct one is Glu-Asp-Pro (EDP).
BioregulatorsProstamax
PreclinicalProstamax is a synthetic Khavinson tetrapeptide (Lys-Glu-Asp-Pro, KEDP) marketed as a prostate bioregulator, conceived as the defined-sequence successor to the older bovine prostate extracts Prostatilen and Vitaprost. It is studied for prostate inflammation and age-related prostate changes, and it has no FDA or EMA approval. Most of the actual clinical prostate evidence belongs to the parent extract, not to the synthetic KEDP peptide itself.
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