Tirzepatide
Tirzepatide
This batch of Tirzepatide Peptide has been third-party lab-tested and verified for quality.
Contents: Tirzepatide (Dual GIP and GLP-1 Receptor Agonist)
Form: Powder
Purity: 99.3%
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Tirzepatide Peptide
Tirzepatide is a synthetic 39-amino-acid peptide that functions as a dual agonist of the glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptors. It is designed to mimic the actions of endogenous incretin hormones, which play a key role in glucose metabolism, energy balance, and appetite regulation. Tirzepatide is being investigated in metabolic and endocrine research as a next-generation incretin-based compound for glycemic control and body-weight modulation.
Overview
Tirzepatide combines GIP and GLP-1 receptor activity within a single molecule, producing additive or synergistic effects on insulin secretion, glucagon suppression, and satiety regulation. Its design includes a C20 fatty diacid moiety attached via a linker at Lys20, allowing reversible albumin binding and prolonged circulation time.
In preclinical and clinical research, Tirzepatide has demonstrated dose-dependent reductions in blood glucose and body weight, along with favorable effects on lipid metabolism and insulin sensitivity. It is of interest for studies exploring integrated incretin signaling, metabolic efficiency, and energy homeostasis.
Chemical Makeup
- Molecular Formula: C225H348N48O68
- Molecular Weight: 4813.5 g/mol
- Amino Acid Sequence: YAEGTFISDYSIAMDKIHQQDFVNWLLAQKGKKNDWKHNITQ (modified GIP/GLP-1 hybrid sequence with C20 fatty diacid side chain at Lys20)
- Compound Class: Dual GIP/GLP-1 receptor agonist
- Form: Lyophilized peptide
- Purity: ≥99% (per COA)
- Sizes Available: 5mg, 10mg, 15mg, 20mg, 30mg vials
Research and Clinical Studies
Glucose Homeostasis
Tirzepatide enhances glucose-dependent insulin secretion while suppressing glucagon release, resulting in improved glycemic profiles. Animal and human studies have shown significant HbA1c reduction compared with selective GLP-1 agonists.
Body-Weight Regulation
Research demonstrates that Tirzepatide influences hypothalamic appetite pathways through dual incretin receptor signaling, leading to reduced energy intake and body-weight loss in preclinical and clinical models.
Insulin Sensitivity and Lipid Metabolism
Tirzepatide has been shown to increase insulin sensitivity in hepatic and peripheral tissues, reduce plasma triglycerides, and improve overall lipid handling in metabolic disease models.
Cardiometabolic and Hepatic Function
Studies indicate that dual incretin activation may reduce systemic inflammation, improve endothelial function, and support hepatic lipid clearance, suggesting cardioprotective and hepatoprotective potential.
Mechanism and Pharmacokinetics
The albumin-binding C20 acyl chain provides an extended elimination half-life (~5 days in primate models), supporting once-weekly administration in long-term metabolic research protocols.
Tirzepatide peptide is available for research and laboratory purposes only. Not for human consumption.
References
- Frias JP, et al. Tirzepatide versus semaglutide in type 2 diabetes. N Engl J Med. 2021;385(6):503–515. https://pubmed.ncbi.nlm.nih.gov/34170647/
- Coskun T, et al. LY3298176, a novel dual GIP and GLP-1 receptor agonist for the treatment of type 2 diabetes. Sci Transl Med. 2018;10(467):eaao6119. https://pubmed.ncbi.nlm.nih.gov/30404864/
- Willard FS, et al. Tirzepatide: discovery and preclinical profile. Cell Metab. 2020;31(3):564–574.e5. https://pubmed.ncbi.nlm.nih.gov/32084394/
- Heise T, et al. Pharmacokinetics and pharmacodynamics of the dual GIP/GLP-1 receptor agonist Tirzepatide. Clin Pharmacokinet. 2022;61(3):359–372. https://pubmed.ncbi.nlm.nih.gov/34694692/
- Drucker DJ. Mechanisms of incretin hormone action. Cell Metab. 2018;27(4):740–756. https://pubmed.ncbi.nlm.nih.gov/29551581/
- Thomas MK, et al. Dual incretin receptor agonists in metabolic research. Diabetes Obes Metab. 2020;22(12):2368–2378. https://pubmed.ncbi.nlm.nih.gov/32706522/
- Heise T, et al. Safety, tolerability, and pharmacology of Tirzepatide in humans. Diabetes Care. 2020;43(12):2910–2918. https://pubmed.ncbi.nlm.nih.gov/32978147/
- Samms RJ, et al. Effects of dual GIP/GLP-1 receptor agonism on energy metabolism. Nat Metab. 2020;2(6):556–563. https://pubmed.ncbi.nlm.nih.gov/32694636/
- Urva SR, et al. Pharmacokinetic and pharmacodynamic modeling of Tirzepatide. Diabetes Obes Metab. 2021;23(1):220–227. https://pubmed.ncbi.nlm.nih.gov/32862523/
- Nauck MA, et al. Incretin therapies and metabolic disease mechanisms. Diabetologia. 2021;64(9):1971–1985. https://pubmed.ncbi.nlm.nih.gov/34050724/
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Peptides in lyophilized (freeze-dried) form are stable at room temperature for transport. Once you receive them, refrigeration is recommended to maintain long-term integrity. We package every order securely to prevent damage and ship promptly, so your vials arrive in optimal condition.
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Store them in the refrigerator, away from direct light and heat. If you need to keep them longer, some peptides can be stored frozen. Each vial comes with clear handling instructions so you know the proper conditions for stability.
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