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MONOGRAPH No. 056
EVIDENCE BASELimited
TYPE
Synthetic tetrapeptide bioregulator
SEQUENCE
Lys-Glu-Asp-Trp
CAS
Not assigned
EU STATUS
Research only
WADA
Not listed
MIN PURITY
≥98% HPLC
Khavinson Bioregulators

Pancragen — EU research guide.

Pancragen is a synthetic tetrapeptide (Lys-Glu-Asp-Trp) from the Khavinson bioregulator series proposed to support beta-cell differentiation and pancreatic tissue gene regulation. It is studied in the same general research context as Suprefort, another pancreas-targeted bioregulator in the same family.

Last reviewed:

What is Pancragen?

Pancragen is a synthetic tetrapeptide (Lys-Glu-Asp-Trp) from the Khavinson bioregulator series proposed to support beta-cell differentiation and pancreatic tissue gene regulation. It is studied in the same general research context as Suprefort, another pancreas-targeted bioregulator in the same family.

What does the research show?

Available research centers on glucose and insulin-related markers in animal models and cell cultures, plus one small non-randomised human comparison (33 patients with type 2 diabetes, 30 controls) from the originating group and collaborators. No independently replicated human trial data is publicly available as of mid-2026, and the proposed mechanism remains far less characterized than established metabolic peptides like GLP-1 analogues.

EU legal status

Not approved as a medicine anywhere in the EU. Sold by a small number of specialist research vendors for laboratory metabolic research only.

⚠ Should not be confused with clinically established diabetes peptide therapies — the evidence base here is preliminary, animal-dominated bioregulator research, not validated metabolic medicine.
✓ Not yet tracked in PeptideCompare's price comparison. Verify any vendor's COA and sequence/identity claims directly before ordering — see our COA guide.
EVIDENCE SUMMARY
LIMITED
Metabolic markers in older adults with type 2 diabetes (small human study) — A 2011 comparative, non-randomised report (30 healthy older controls, 33 older patients with type 2 diabetes; not described as blinded) found nocturnal melatonin output reduced by 70% in the diabetic group. In the diabetic patients who received Pancragen, fasting glucose, insulin and insulin-resistance indices fell and glucose tolerance improved, while diabetic controls without it showed no change. Group split and duration were not verified, and the work has not been independently replicated.
ANIMAL ONLY
Streptozotocin diabetes in rats — In Wistar rats with streptozotocin-induced diabetes (2007), the Khavinson group reported a pronounced glucose-lowering effect with oral administration and normalised endothelial adhesion with intramuscular administration, but no effect on vascular permeability. Group sizes were not verified.
LIMITED
Pancreatic cell cultures (in vitro) — A 2013 paper reports that Pancragen increased expression of differentiation factors such as Pdx1 and Ptf1a (acinar cells) and Pdx1, Pax6, Pax4, Foxa2 and Nkx2.2 (islet cells) in young and aged pancreatic cell cultures. This is expression-marker work in culture, not a demonstration of function in a living organism.

Molecular information

CAS number
Not assigned

Pharmacokinetics

No established human pharmacokinetic data. Published human PK parameters for this compound are not available; reported data are limited to animal models or absent. No curve is shown, to avoid implying data that does not exist.

Potency retained over time

Each line is one storage condition: it starts at 100% and falls as potency is lost. Above the dashed 80% line the material is considered reliable — hover for exact values.

Freezer −20 °C
36+ mo
Stable · >95% potency
Fridge 4 °C
3-4 mo
In use · after recon
Room 20 °C
2-3 wks
Limited · moderate loss
Warm 37 °C+
2-3 days
Critical · rapid degradation

⚠ A structural estimate, derived from each compound's sequence length, cyclisation and oxidation-, deamidation- and light-sensitive residues. Indicative only — not lab-measured per batch.

Pancragen is not yet in our price comparison

We expand EU supplier coverage every month.

References

  1. Small comparative human study (30 controls, 33 type 2 diabetes patients) co-authored by Khavinson. It reports improved glucose and insulin markers with Pancragen, but is not described as randomised or blinded and I could not verify group sizes per arm or duration. Treat it as hypothesis-generating. Korkushko OV, Khavinson VKh, Shatilo VB, Antonyk-Sheglova IA, Bondarenko EV. Prospects of using Pancragen for correction of metabolic disorders in elderly people. Bull Exp Biol Med. 2011;151(4):454-456. DOI
  2. Rat study in streptozotocin diabetes: glucose lowering and normalised endothelial adhesion were reported. Animal data from the originating group only; it does not show that the effect carries over to people. Khavinson VKh, Gavrisheva NA, Malinin VV, Chefu SG, Trofimov EL. Effect of pancragen on blood glucose level, capillary permeability and adhesion in rats with experimental diabetes mellitus. Bull Exp Biol Med. 2007;144(4):559-562. DOIPubMed 18642713
  3. Cell-culture study: Pancragen raised expression of pancreatic differentiation transcription factors in young and aged cultures. It is a mechanism hint at best, from the originating group. Khavinson VK, Durnova AO, Polyakova VO, et al. Effects of Pancragen on the differentiation of pancreatic cells during their ageing. Bull Exp Biol Med. 2013;154:501-504. DOI
  4. Study of the endogenous tetrapeptide Lys-Glu-Asp-Trp-NH2, including a chemically induced diabetes model and programmed-cell-death markers. Only the abstract summary was checked; model species and results in detail were not verified. Khavinson VKh, Gapparov MM, Sharanova NE, Vasilyev AV, Ryzhak GA. Study of biological activity of Lys-Glu-Asp-Trp-NH2 endogenous tetrapeptide. Bull Exp Biol Med. 2010;149(3):351-353. DOIPubMed 21246099

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