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Peptide Database

Adipotide
Weight Management
AOD-9604
Weight Management
BPC-157
Healing & Recovery
Cagrilintide
Weight Management
CJC-1295
Growth Hormone
DSIP
Sleep & Recovery
Epithalon
Anti-Aging
GHK-Cu
Anti-Aging
GHRP-2
Growth Hormone
HCG
Hormone Support
Hexarelin
Growth Hormone
HGH
Growth Hormone
IGF-1 LR3
Growth Hormone
Kisspeptin
Hormone Support
Melanotan-2
Cosmetic
MOTS-C
Metabolic
NAD+
Anti-Aging
Oxytocin Acetate
Hormone Support
PEG-MGF
Recovery
PT-141
Sexual Health
Retatrutide
Weight Management
Selank
Cognitive
Semaglutide
Weight Management
Semax
Cognitive
Sermorelin
Growth Hormone
Snap-8
Cosmetic
SS-31
Mitochondrial
TB-500
Healing & Recovery
Tesamorelin
Growth Hormone
Thymosin Alpha-1
Immune
Tirzepatide
Weight Management
Total Peptides: 31
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Adipotide
Max Weight Loss14.7%
Studies2
Participants48
StatusLimited

Adipotide

Prohibitin-targeting peptide 1 (Prohibitin-TP01)

Adipotide is a revolutionary experimental vascular-targeting peptidomimetic designed to induce selective apoptosis in blood vessels supplying white adipose tissue. Also known as Prohibitin-TP01, FTPP (Fat-Targeted Proapoptotic Peptide), or TP-1, it represents a completely novel approach to weight management through direct fat cell elimination rather than appetite suppression. While clinical development was discontinued in 2019 due to nephrotoxicity concerns, preclinical studies demonstrated remarkable efficacy with up to 30% weight reduction in rodent models and 11% weight loss in primate studies over just 28 days.

Clinical Benefits

Direct fat cell elimination via vascular disruption
Significant weight loss (11% in 28-day primate studies)
38.7% reduction in total body fat percentage (primate data)
Preserved lean muscle mass during rapid fat loss
Improved insulin sensitivity independent of weight loss
Enhanced glucose tolerance and metabolic function

Mechanism of Action

Adipotide employs a unique dual-domain architecture for targeted adipose tissue elimination. The N-terminal CKGGRAKDC targeting domain functions as a vascular homing peptide that binds specifically to prohibitin-1 and annexin A2 (ANXA2) receptors highly expressed on endothelial cells of blood vessels supplying white adipose tissue. Following receptor-mediated binding and cellular internalization, the C-terminal D(KLAKLAK)₂ proapoptotic domain disrupts mitochondrial membranes through cationic amphipathic peptide interactions, triggering cytochrome c release and caspase-dependent apoptosis. This leads to endothelial cell death, vascular regression, and subsequent secondary apoptosis of downstream adipocytes due to ischemia and nutrient deprivation. The process is highly selective for white adipose tissue vasculature due to the specific expression pattern of prohibitin-1 receptors.

Key Action: Vascular-targeting peptide - destroys blood vessels feeding fat tissue causing direct fat cell elimination

Proven Results

%
Maximum Weight Loss
Clinical research data
0%
Diabetes Risk Reduction
Clinical research data
48
Total Participants
Research studies
0%
CV Risk Reduction
Clinical data

Medical Disclaimer

CRITICAL WARNING: Adipotide clinical development was permanently discontinued due to unacceptable nephrotoxicity. All human trials were terminated early. This information is for educational purposes only. Adipotide is NOT approved for any human use and carries severe kidney damage risks. Consult healthcare providers for approved weight management alternatives.