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Reference: RETADPEN10

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Retatrutide is a powerful triple agonist peptide that targets GLP-1, GIP (glucose-dependent insulinotropic polypeptide), and glucagon receptors—making it the most comprehensive metabolic peptide in its class. It builds on the progress of earlier compounds like Semaglutide and Tirzepatide by activating three key hormonal pathways involved in appetite...
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Retatrutide is a powerful triple agonist peptide that targets GLP-1, GIP (glucose-dependent insulinotropic polypeptide), and glucagon receptors—making it the most comprehensive metabolic peptide in its class. It builds on the progress of earlier compounds like Semaglutide and Tirzepatide by activating three key hormonal pathways involved in appetite...
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Reference: v3penblk

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Adipotide 10mg
  • Adipotide 10mg

Adipotide 10mg

Adipotide is a high-purity compound studied for neuroprotection and cognitive enhancement. Research explores its role in supporting neuronal function and resilience, while also examining metabolic regulation and adipocyte-targeting effects in experimental models of obesity and energy balance.

For research purposes only. This product is supplied exclusively for scientific laboratory research and analytical purposes. It is not intended for human or animal use, and must not be misused in any way that contravenes MHRA regulations or applicable laws.

£44.90
VAT included
Delivered within 1-3 days
Quantity
In Stock
6 Items

Description

Adipotide (aka prohibitin-TP01 and fat-targeted proapoptotic peptide) designed to selectively eliminate blood vessels feeding white adipose (fat) tissue. It combines a homing sequence that targets fat-vasculature receptors (e.g. prohibitin/annexin A2) and a pro-apoptotic (cell death-inducing) sequence that triggers vessel cell death. The mechanism aims to starve fat cells of blood supply, leading to targeted fat tissue loss rather than systemic appetite suppression. Once the fat tissue has undergone apoptosis, it is cleared by the body. These results happen regardless of whether or not a person changes their diet or exercise regimens.

  • Targeted visceral fat reduction: Adipotide preferentially affected white adipose tissue, including visceral fat around organs. Visceral fat is linked to cardiovascular diseases, diabetes, and metabolic risk- reducing it can have outsized health benefits compared to losing general body weight.
  • Improved insulin support, for Type 2 diabetics
  • Because the targeting receptor, prohibitin, is also present in some tumor vasculature, it is of interest to cancer researchers
  • Its non-CNS peripheral action provides a mechanistic contrast to central appetite-modulating drugs

  • Injection site reactions (redness, swelling, and/or itching)
  • Loss of appetite
  • Fatigue
  • Dizziness
  • Electrolyte imbalance
  • Dehydration
  • Dose-dependent, predictable, reversible renal injury and tubular dysfunction, including minimal to moderate tubular degeneration and necrosis after treatment, typically resolved after treatment.
  • Increased urine output and slight dehydration have been observed, potentially reflecting early kidney function disruption
  • Serum creatinine elevation indicate kidney strain, although typically mild and reversible
  • Dehydration common, potentially linked to increased diuresis and kidney changes

  • Co-administration with other nephrotoxic agents (e.g. aminoglycosides, certain chemotherapeutics, high-dose contrast agents) could theoretically increase the risk of combined kidney toxicity.
  • Because Adipotide influences fat tissue metabolism and possibly insulin sensitivity, theoretical interactions with glucose-lowering medications (e.g. insulin or hypoglycemic agents) or lipid-modifying agents could occur, although no controlled data exist.

  • Do not use if pregnant or breastfeeding
  • Do not use if you have pre-existing renal impairment. Can be particularly hard on the kidneys.

28-day cycle followed by 12-28 day washout period

Daily dosing for duration of the cycle 

May be dosed at any time, day or night

Adipotide does not have to be taken in a fasted state

Subcutaneous administration: abdominal region recommended

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