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Home Limitless Pancragen Peptide (Lys-Glu-Asp-Trp) 20mg
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Pancragen Peptide (Lys-Glu-Asp-Trp) 20mg

$62.00

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Category: Limitless Tags: Pancragen, Pancragen Peptide, Pancragen Peptide (Lys-Glu-Asp-Trp) 20mg, Pancragen Peptide 20mg, what is Pancragen Peptide
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Description

Pancragen Peptide Description

Pancragen is a tetrapeptide bioregulator composed of the amino acid sequence Lys-Glu-Asp-Trp (KEDW). This laboratory-grade peptide demonstrates significant biological activity in experimental settings, particularly in pancreatic cell culture studies.

Research indicates that Pancragen exhibits notable effects on pancreatic function and glucose metabolism at nanomolar concentrations. The pancreas peptide has been shown to help normalize insulin production and improve pancreatic beta cell regeneration in experimental models, suggesting potential applications in metabolic research.

Pancragen’s mechanism of action appears to involve modulation of gene expression in pancreatic tissues, potentially activating regenerative pathways that support cellular rejuvenation. The peptide demonstrates tissue-specific affinity with minimal off-target effects in laboratory investigations.

This specialized bioregulator represents a valuable research tool for laboratories studying pancreatic function, insulin signaling pathways, and age-related changes in glucose metabolism. Pancragen offers researchers a well-characterized compound for investigating pancreatic cellular resilience and metabolic regulation.

Peptide Specifications

  • Sequence: Lys-Glu-Asp-Trp (KEDW)
  • Molecular Formula: C₂₆H₃₆N₆O₉
  • Molecular Weight: 576.25 g/mol
  • PubChem CID: 68452887
  • Synonyms: SCHEMBL5491754
  • IUPAC Name: (4S)-5-[[(2S)-3-carboxy-1-[[(1S)-1-carboxy-2-(1H-indol-3-yl)ethyl]amino]-1-oxopropan-2-yl]amino]-4-[[(2S)-2,6-diaminohexanoyl]amino]-5-oxopentanoic acid
  • Storage: Store in lyophilized form at or below -20°C

Research Applications

  • Pancreatic Endocrine Function
  • Glucose Metabolism
  • Geroprotection and Tissue Aging
  • Diabetes Research

Legal Disclaimer

This product is sold as a pure compound for research purposes only and is not meant for use as a dietary supplement. Please refer to our terms and conditions prior to purchase.

Safety Information: Keep this product out of the reach of children. This material has limited research available about it and may result in adverse effects if improperly handled or consumed. This product is not a dietary supplement, but a pure substance, sold as a raw material. We attest exclusively to the quality, purity and description of the materials we provide. This product is for use and handling only by persons with the knowledge and equipment to safely handle this material. You agree to indemnify us for any adverse effects that may arise from improper handling and/or consumption of this product.

The articles and information on products that may be found on this website are provided exclusively for the purposes of providing information and education. These items are not pharmaceuticals or medications, and the Food and Drug Administration has not given permission for the treatment or prevention of any disease, medical condition, or ailment using them.

Research

Research

Pancragen has been studied for its potential to restore function of the pancreas in the context of aging and type 2 diabetes. Research has focused on its effects in animal models, examining both endocrine regulation and cellular differentiation in the pancreas.

Mechanisms of Action

In human embryonic pancreatic cell cultures, pancragen specifically stimulated the expression of differentiation factors (CXCL12, Hoxa3), especially in aged cells. This tissue-specific stimulation was more pronounced in older cultures, indicating a possible geroprotective mechanism.[1]

Effects on Pancreatic Endocrine Function

In older animals, pancragen administration led to decreased basal insulin and C-peptide levels, increased glucose disappearance rates, and normalization of glucose, insulin, and C-peptide responses after glucose administration. These effects partially persisted for three weeks after stopping treatment.[2]

Pancragen was effective in restoring age-related endocrine dysfunctions of the pancreas, suggesting its promise as a therapeutic agent for age-associated glucose intolerance and type 2 diabetes.[2]

Effectiveness in Diabetes Models

In elderly patients with type 2 diabetes, pancragen administration led to significant reductions in fasting glucose, improved glucose tolerance, and decreased insulin resistance. These benefits were not observed in patients who did not receive pancragen, suggesting a specific therapeutic effect.[3] 

In diabetic rats, pancragen normalized the adhesion of mesenteric capillary endothelium, suggesting protective effects on vascular function during early diabetes, though it did not affect capillary permeability.[4] 

Oral pancragen produced a significant hypoglycemic effect during treatment, supporting its potential for blood glucose regulation in diabetes. The peptide also demonstrated homeostatic effects in diabetic conditions, further supporting its research potential.[4]

References

  1. Khavinson, V., Linkova, N., Polyakova, V., Kheifets, O., Tarnovskaya, S., & Kvetnoy, I. (2012). Peptides Tissue-Specifically Stimulate Cell Differentiation during Their Aging. Bulletin of Experimental Biology and Medicine, 153, 148-151. https://doi.org/10.1007/s10517-012-1664-1.
  2. Goncharova, N., Ivanova, L., Oganian, T., Vengerin, A., & Khavinson, V. (2014). [Impact of tetrapeptide pancragen on endocrine function of the pancreas in old monkeys].. Advances in gerontology = Uspekhi gerontologii, 27 4, 662-7.
  3. Korkushko, O., Khavinson, V., Shatilo, V., Antonyk-Sheglova, I., & Bondarenko, E. (2011). Prospects of Using Pancragen for Correction of Metabolic Disorders in Elderly People. Bulletin of Experimental Biology and Medicine, 151, 454-456. https://doi.org/10.1007/s10517-011-1354-4.
  4. Khavinson, V., Gavrisheva, N., Malinin, V., Chefu, S., & Trofimov, E. (2007). Effect of pancragen on blood glucose level, capillary permeability and adhesion in rats with experimental diabetes mellitus. Bulletin of Experimental Biology and Medicine, 144, 559-562. https://doi.org/10.1007/s10517-007-0377-3.
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