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SYS · ONLINEPASS · 63.0%
Open Assay
Independent Testing / Est. 2026
BATCH04·26·B
PASS63.0%
N27
PeptidesLongevityVesugen

Vesugen

/ Khavinson-tradition tripeptide (Lys-Glu-Asp); proposed vascular endothelium bioregulator
SPECULATIVEN = 0 · TESTING PENDINGMW 391.40 g·mol⁻¹

ALIAS · KED · Lys-Glu-Asp · Vascular peptide bioregulator

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Research use onlyAny dose figures below describe what specific cited studies used, reported factually. Nothing on this page is guidance for human use.READ FIRST →

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§ A · Identity
Primary sequenceKED
MW · 391.40CLASS · Khavinson-tradition tripeptide (Lys-Glu-Asp); proposed vascular endothelium bioregulatorCATEGORY · Longevity

Tier 4. Vesugen is the trade designation in the Khavinson school for the synthetic tripeptide Lys-Glu-Asp (KED), proposed as a vascular-endothelium peptide bioregulator. The molecule is a defined chemical entity (unlike fractionated cytogen extracts), but its proposed pharmacology rests on the Khavinson laboratory's broader peptide-bioregulator hypothesis and has not been independently replicated under contemporary Western trial methodology.

§ B · Mechanism of action

The Khavinson programme proposes that short peptides such as KED bind directly to specific DNA sequences and modulate transcription in a tissue-selective manner, with KED specifically positioned as a vascular-endothelium regulator. Cell-culture and rodent studies from the Saint Petersburg group describe effects on endothelial gene expression, vascular wall remodelling markers, and age-related vascular function; the mechanistic framework (direct DNA binding by tripeptides) remains a single-school claim that the broader transcription-factor literature has not adopted.

§ C · Human clinical evidence

Tier 4. The published evidence base is dominated by the Khavinson group's own primary work, much of which appears in Russian-language journals and review chapters. PubMed-indexed English-language KED tripeptide literature is sparse and largely descriptive. No Phase 1 or later trial in Western literature.

§ F · Safety signal

No formal Phase 1 human safety database in Western literature. Russian sources report good tolerability within the bioregulator clinical tradition.

§ H · Regulatory status

Regulatory status

FDA status:
Not FDA-approved
§ I · Notable gaps and controversies

Russian-origin literature without independent Western replication. The proposed direct-DNA-binding mechanism for short peptides is a foundational claim of the Khavinson programme that remains controversial outside it. Vendor-sold KED material is sold as a chemically defined tripeptide but the pharmacological claims accompanying it derive from the unreplicated bioregulator literature.