Weight Loss
Retatrutide 10mg
$89.99Retatrutide 10 mg is a next-generation triple-agonist peptide developed by Eli Lilly that simultaneously activates GLP-1, GIP, and glucagon receptors. This advanced multi-receptor approach distinguishes retatrutide from earlier weight-management compounds by targeting appetite control, insulin regulation, energy expenditure, and fat oxidation together, making it a key focus in metabolic and obesity research.
Retatrutide 20mg
$139.99Retatrutide 20 mg is a higher-dose research format of retatrutide, an investigational triple-agonist peptide developed by Eli Lilly that simultaneously targets the GLP-1, GIP, and glucagon receptors. This dosage is commonly discussed in research contexts exploring more pronounced metabolic signaling, dose-response relationships, energy regulation, and coordinated activation of multiple metabolic pathways.
Retatrutide 5mg
$49.99Retatrutide, developed by Eli Lilly, is a next-generation triple agonist peptide that simultaneously activates GLP-1, GIP, and glucagon receptors. This multi-receptor approach differentiates retatrutide from earlier weight-management therapies by targeting appetite regulation, insulin signaling, energy expenditure, and fat oxidation in parallel, making it a major focus of advanced metabolic and obesity research.
Retatrutide 60mg
$299.99Retatrutide 60 mg is a higher-strength research format of retatrutide, an investigational triple-agonist peptide developed by Eli Lilly that simultaneously targets the GLP-1, GIP, and glucagon receptors. In research contexts, this higher-strength format may be discussed in studies examining metabolic signaling, dose-response relationships, energy regulation, receptor activity, and coordinated engagement of multiple metabolic pathways.
Tesamorelin 10mg
$89.99Tesamorelin is a stabilized synthetic analog of growth hormone–releasing hormone (GHRH 1–44) featuring a trans-3-hexenoic acid modification that improves peptide stability. In experimental settings, tesamorelin binds to GHRH receptors to stimulate endogenous growth hormone synthesis and secretion. It is widely used in endocrine and metabolic research focused on peptide stability, receptor binding kinetics, and modulation of the somatotropic (GH) axis.
Tesamorelin 20mg
$149.99Tesamorelin 20 mg is a higher-strength research format of tesamorelin, a stabilized synthetic analog of growth hormone–releasing hormone (GHRH) that acts on pituitary GHRH receptors to stimulate endogenous growth hormone (GH) secretion. Originally developed by Theratechnologies, tesamorelin has been extensively investigated in endocrine, metabolic, and body-composition research, particularly in studies involving the somatotropic GH–IGF-1 axis.
Tesamorelin 5mg
$29.99Tesamorelin 5 mg is a research format of tesamorelin, a stabilized synthetic analog of growth hormone–releasing hormone (GHRH) designed to stimulate endogenous growth hormone (GH) secretion through activation of pituitary GHRH receptors. Originally developed by Theratechnologies, tesamorelin has been extensively investigated in endocrine, metabolic, and body-composition research, particularly in studies involving the somatotropic GH–IGF-1 axis.
Tirzepatide 20mg
$109.99Tirzepatide is a synthetic peptide developed by Eli Lilly that acts on two important incretin receptors: GLP-1 (glucagon-like peptide-1) and GIP (glucose-dependent insulinotropic polypeptide). By engaging both pathways, tirzepatide provides researchers with a valuable model for investigating appetite regulation, glucose metabolism, insulin signaling, energy balance, and body-weight biology. Tirzepatide 20 mg represents a higher-strength research format and should not be interpreted as a recommended clinical dosage.
Tirzepatide 60mg
$299.99Tirzepatide is a synthetic peptide developed by Eli Lilly that simultaneously targets two incretin receptors: GLP-1 (glucagon-like peptide-1) and GIP (glucose-dependent insulinotropic polypeptide). This combined mechanism has made tirzepatide an important subject in metabolic research, particularly in studies of appetite regulation, glucose homeostasis, insulin signaling, energy balance, and body-weight regulation. The 60 mg designation represents a research-format quantity and should not be considered an established or recommended clinical dosage.
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