Need help? Call Or Text us, and a team member will be happy to assist you. +1 (570) 539-9711

Need help? Call Or Text us, and a team member will be happy to assist you.
+1 (570) 539-9711

  • Tirzepatide is a dual agonist targeting the glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptors—novel dual incretin-based therapy. Its design integrates both GLP-1 and GIP actions in a single molecule, enhancing insulin secretion, reducing glucagon levels, delaying gastric emptying, and promoting satiety through central nervous system pathways.
  • Tirzepatide is a dual agonist targeting the glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptors—novel dual incretin-based therapy. Its design integrates both GLP-1 and GIP actions in a single molecule, enhancing insulin secretion, reducing glucagon levels, delaying gastric emptying, and promoting satiety through central nervous system pathways.
  • Triple receptor agonist: Retatrutide (also known as LY-3437943) simultaneously targets three receptors GLP-1, GIP, and glucagon (GCG). This sets it apart from single (e.g., semaglutide) or dual agonists (e.g., tirzepatide)
  • Triple receptor agonist: Retatrutide (also known as LY-3437943) simultaneously targets three receptors GLP-1, GIP, and glucagon (GCG). This sets it apart from single (e.g., semaglutide) or dual agonists (e.g., tirzepatide)
  • Triple receptor agonist: Retatrutide (also known as LY-3437943) simultaneously targets three receptors GLP-1, GIP, and glucagon (GCG). This sets it apart from single (e.g., semaglutide) or dual agonists (e.g., tirzepatide)
  • Triple receptor agonist: Retatrutide (also known as LY-3437943) simultaneously targets three receptors GLP-1, GIP, and glucagon (GCG). This sets it apart from single (e.g., semaglutide) or dual agonists (e.g., tirzepatide)
  • IGF-1 LR3 (Insulin-like Growth Factor-1 Long R3) is a synthetic, engineered variant of insulin-like growth factor-1 designed for enhanced stability and activity. Unlike native IGF-1, IGF-1 LR3 has a reduced affinity for IGF-binding proteins, allowing it to remain biologically active for up to 120 times longer. This extended half-life increases its physiological impact, promoting enhanced cell proliferation, fat metabolism, and muscle growth through the suppression of myostatin. Additionally, emerging studies indicate potential applications in supporting lactation in postpartum mothers.
  • Ipamorelin is a synthetic pentapeptide originally developed by Novo Nordisk as part of their exploration of selective growth hormone secretagogues. Structurally, it is a short chain of five amino acids, designed to act as an agonist at the ghrelin or growth hormone secretagogue receptor (GHS-R1a). By binding to this receptor in the hypothalamus and pituitary gland, ipamorelin mimics the activity of the natural “hunger hormone” ghrelin, stimulating the pituitary to release growth hormone (GH) in a pulsatile and physiologically natural rhythm. This mechanism contrasts with direct growth hormone injections, which deliver GH in a non-pulsatile, supra-physiological manner.
  • Kisspeptin plays a key role in regulating hormone secretion involved in reproduction. It has been shown to impact testosterone levels as well as sex-related behaviors such as libido and motivation. Emerging research also indicates that kisspeptin may counteract certain effects of aging.
  • Kisspeptin plays a key role in regulating hormone secretion involved in reproduction. It has been shown to impact testosterone levels as well as sex-related behaviors such as libido and motivation. Emerging research also indicates that kisspeptin may counteract certain effects of aging.
  • KPV 10mg

    $69.99
    KPV is a synthetic tripeptide (a short chain of three amino acids: lysine-proline-valine) that is derived from the larger hormone alpha-melanocyte stimulating hormone (α-MSH). It is a small peptide drug candidate with strong anti-inflammatory and protective properties, derived from the larger α-MSH hormone, and is being investigated as a targeted therapy for inflammatory disorders.
  • MOTS-c is a 16–amino acid mitochondrial-derived peptide (MDP) that plays a key role in metabolic regulation. Produced within mitochondria, it helps maintain cellular energy balance by influencing glucose metabolism, insulin sensitivity, and stress-response pathways. MOTS-c can translocate to the nucleus, where it regulates the expression of genes involved in mitochondrial biogenesis and metabolic adaptation, particularly during metabolic stress. Studies indicate that MOTS-c enhances exercise performance, reduces obesity and insulin resistance, and provides protective effects against conditions such as osteoporosis, metabolic disorders, and age-related diseases. In summary, MOTS-c supports metabolic homeostasis, healthy aging, and improved physical performance while mitigating the risk of obesity, insulin resistance, and related disease states.
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