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.
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.
ADDITIONAL BENEFITS
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
POSSIBLE SIDE EFFECTS
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
INTERACTIONS
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.
CONTRAINDICATIONS
Do not use if pregnant or breastfeeding
Do not use if you have pre-existing renal impairment. Can be particularly hard on the kidneys.
ADIPOTIDE: 10MG – CYCLE AND DOSING CONSIDERATIONS
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
Chemical Information
• Synonyms: Adipotide, HKPao • CAS Number: 859216-15-2 • Molecular Formula: C111H206N36O28S2 • Form: Lyophilized powder, 5mg per vial • Purity: ≥99% (Peptide-grade) • Storage: Store at 2–8°C, protected from light and moisture
Product Assurance
✅ HPLC Verified – Ensuring ≥99% purity ✅ COA Provided – On Request ✅ Manufactured in a GMP-Certified Facility - Developed & Dispatched in the UK ✅ Third-Party Testing Covered – Independent Verification Available on Request ✅ Cold Chain Express Delivery – Ensuring Potency, Integrity & Safe Arrival
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