
Metabolic Research Stack
Three Vials, One Research Focus
The METABOLIC+ Bundle assembles three metabolically focused research compounds. Tirzepatide is a dual GIP and GLP-1 receptor agonist, characterised in a 2018 Lancet trial[2]. AOD-9604 is a modified C-terminal fragment (176-191) of human growth hormone, studied as a synthetic lipolytic domain[3]. Tesamorelin is a stabilised GHRH analogue whose metabolic effects were characterised in a 2007 New England Journal of Medicine trial[5].
- Three metabolic research pathways in one set
- Tirzepatide — dual GIP/GLP-1 incretin signalling
- AOD-9604 — hGH fragment 176-191, lipolysis research
- Tesamorelin — GHRH analogue, visceral-fat research
- Lot-specific third-party COA for each compound

Inside the Bundle
What's in the Stack
The bundle ships as three separate lyophilized vials: Tirzepatide 10 mg, AOD-9604 5 mg and Tesamorelin 10 mg. The three compounds cover distinct arms of metabolic research: incretin-receptor signalling (tirzepatide, whose weight-related outcomes were reported in the SURMOUNT-1 trial[1]), growth-hormone-fragment lipolysis (AOD-9604[3]) and GHRH-axis signalling (tesamorelin[5]).
- Tirzepatide — 10 mg lyophilized vial
- AOD-9604 — 5 mg lyophilized vial
- Tesamorelin — 10 mg lyophilized vial
- Incretin + lipolysis + GHRH-axis research coverage
- 10% saving versus buying the three vials separately

Research Applications
Areas of Scientific Investigation
Each compound carries its own line of evidence: in clinical trials, tirzepatide produced substantial weight reduction in adults with obesity[1]; in obese-mouse studies, chronic treatment with the hGH C-terminal fragment increased fat oxidation and weight loss[4]; and tesamorelin reduced liver fat in a randomised trial in people with HIV[6]. No published study evaluates the three compounds in combination; researchers using them side by side are combining independent lines of evidence.
- Incretin-receptor and glucose-homeostasis research
- Lipolysis and fat-oxidation assays
- GHRH-axis and body-composition studies
- Energy-balance and appetite-signalling models

Understanding the Metabolic+ Stack: Mechanism of Action
Tirzepatide is structurally distinct from single-target incretin peptides: it activates both GLP-1 and GIP receptors. Its efficacy and safety as a dual agonist were characterised in a 2018 Lancet dose-ranging trial[2], and in the SURMOUNT-1 trial it produced substantial, dose-dependent weight reduction in adults with obesity[1].
AOD-9604 is a modified synthetic analogue of the C-terminal region (amino acids 176-191) of human growth hormone — the segment associated with hGH's lipolytic activity — without the whole hormone's growth-promoting signalling. It was characterised as a synthetic lipolytic domain in metabolic studies[3], and chronic treatment increased fat oxidation and weight loss in obese-mouse models[4].
Tesamorelin is a stabilised analogue of growth-hormone-releasing hormone (GHRH). In randomised clinical trials it reduced visceral adipose tissue in patients with HIV-associated lipodystrophy[5] and reduced liver fat in a randomised, double-blind trial in people with HIV[6].
Together, the three vials cover three independent arms of metabolic research: incretin-receptor signalling, growth-hormone-fragment lipolysis and GHRH-axis stimulation. Each arm is supported by its own line of published evidence; no published study evaluates the combination itself. These materials are supplied strictly for laboratory research use.
Scientific Literature
- Jastreboff AM, Aronne LJ, Ahmad NN, et al. Tirzepatide once weekly for the treatment of obesity. N Engl J Med. 2022;387(3):205-216.
- Frias JP, Nauck MA, Van J, et al. Efficacy and safety of LY3298176, a novel dual GIP and GLP-1 receptor agonist, in patients with type 2 diabetes. Lancet. 2018;392(10160):2180-2193.
- Ng FM, Sun J, Sharma L, Libinaka R, Jiang WJ, Gianello R. Metabolic studies of a synthetic lipolytic domain (AOD9604) of human growth hormone. Horm Res. 2000;53(6):274-8.
- Heffernan MA, Thorburn AW, Fam B, et al. Increase of fat oxidation and weight loss in obese mice caused by chronic treatment with human growth hormone or a modified C-terminal fragment. Int J Obes Relat Metab Disord. 2001;25(10):1442-9.
- Falutz J, Allas S, Blot K, et al. Metabolic effects of a growth hormone-releasing factor in patients with HIV. N Engl J Med. 2007;357(23):2359-70.
- Stanley TL, Fourman LT, Feldpausch MN, et al. Effects of tesamorelin on non-alcoholic fatty liver disease in HIV: a randomised, double-blind, multicentre trial. Lancet HIV. 2019;6(12):e821-e830.
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METABOLIC+ Bundle
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$225.00$405.00
- ≥99%96%
- 3 vials3 vials
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