Adipotide

Emerging

Chimeric peptidomimetic

Adipotide is a targeting pro-apoptotic peptide that has been studied in preclinical obesity research for its effects on white adipose tissue. It has been investigated for its ability to selectively target and induce apoptosis in adipose tissue vasculature through integrin receptor binding. Published research has examined its effects on body weight and metabolic parameters in animal models. RaysunPeptide supplies Adipotide for qualified research and laboratory applications.

Mechanism of Action

CKGGRAKDC ligand homes to prohibitin/annexin A2 on white-fat endothelium; linked D-(KLAKLAK)2 disrupts mitochondrial membranes post-internalization, triggering localized endothelial apoptosis and adipocyte loss.

Key Benefits

1Rapid fat-mass reduction via selective white adipose tissue vascular targeting
2Improved insulin sensitivity following adipose reduction
3Non-CNS peripheral mechanism distinct from appetite suppressants

Molecular Data

Molecular Weight
N/A
Half-Life
Not established
Chain Length
N/A
Amino Acid Sequence
CKGGRAKDC-GG-D(KLAKLAK)2

Dosing Protocols

GoalDoseFrequencyRoute
Primate Research Replication0.43 mg/kgOnce dailySubQ
Dose-Finding (Research)0.10-0.75 mg/kgOnce daily (escalating tiers)SubQ

Research Indications

Weight Loss

Adipose Mass Reductionmost effective

Selective white adipose tissue vascular targeting produced 7-15% body-weight loss over 4 weeks in obese macaques.

Metabolic

Insulin Resistanceeffective

Improved insulin response (reduced insulin AUC) following fat-mass reduction in primates.

Appetite Control

Non-CNS Mechanismmoderate

Weight loss without primary appetite suppression; peripheral vascular approach.

Peptide Interactions

Semaglutide~ monitor

Potential additive dehydration/GI effects; monitor renal function.

Tirzepatide~ monitor

Overlapping weight-loss effects; monitor kidney function, volume status, electrolytes.

Cagrilintide~ monitor

No clinical data on co-administration; mechanisms differ.

AOD-9604~ monitor

No published data on combined use or pharmacodynamic interaction.

BPC-157+ compatible

No known direct interaction; distinct mechanisms and targets.

CJC-1295/Ipamorelin~ monitor

Metabolic effects may confound body-composition endpoints.

Melanotan II~ monitor

Theoretical vascular/pressor effects; stagger dosing, monitor BP and hydration.

Nephrotoxic Drugs! avoid

Adipotide shows dose-dependent proximal tubule injury; avoid additional renal insults.

What to Expect

1
Week 1-2
Early reduction in abdominal circumference
2
Week 2-4
Progressive weight/fat-mass decline
3
Post-Discontinuation
Partial rebound possible; lab signals include mild creatinine rise and electrolyte shifts

Side Effects & Safety

Common (Generally Mild)

  • •Mild creatinine elevation
  • •Electrolyte shifts
  • •Dose-dependent proximal tubule changes (reversible in primates)

Stop Signs (Seek Medical Attention)

  • ⚠Sustained creatinine elevation or oliguria
  • ⚠Progressive electrolyte abnormalities
  • ⚠Severe injection-site reactions or systemic symptoms
  • ⚠Unexpected toxicity

Contraindications

  • ✕Pregnancy/lactation (not studied)
  • ✕Dehydration
  • ✕Concurrent nephrotoxic medications

Quality Checklist

Good Signs ✓

  • Intact lyophilized cake - white, uniform indicates proper lyophilization
  • Clear solution - fully dissolved, particle-free after reconstitution

Warning Signs !

  • Minor clumping may form from shipping; should dissolve with gentle swirl

Bad Signs ✕

  • Collapsed/moist cake suggests temperature excursion; do not use without QC
  • Cloudiness/precipitate indicates degradation or contamination—discard

References

A peptidomimetic targeting white fat causes weight loss and improved insulin resistance in obese monkeys
• • 2011

Rhesus macaques at 0.43 mg/kg SC daily for 28 days showed 7.4-14.7% weight loss; insulin resistance improved; mild, dose-dependent, reversible proximal tubule changes.

Reversal of obesity by targeted ablation of adipose tissue
• • 2004

Mice with diet-induced obesity showed ~30% weight reduction; adipose vascular apoptosis; metabolic normalization.

Prohibitin/Annexin A2 Interaction Regulates Fatty-Acid Transport
• • 2016

Mechanistic validation of prohibitin/ANXA2 axis in adipose tissue, core to TP01 targeting.

Mixed-Chirality Prohibitin Peptide: D-(RLARLAR)2 Enhances Stability
• • 2025

Next-generation prohibitin constructs improve serum stability and efficacy vs. first-generation TP01.

FAQs

How does Adipotide's weight loss mechanism differ from semaglutide?

Adipotide targets adipose tissue vascular endothelium directly, causing localized endothelial apoptosis and adipocyte loss via a peripheral vascular mechanism. Semaglutide suppresses appetite centrally via GLP-1 receptors. Adipotide achieves weight loss without appetite suppression, making it mechanistically distinct from appetite suppressants.

What kidney safety concerns halted Adipotide's Phase 1 development?

Phase 1 trials showed dose-dependent mild creatinine elevation and reversible proximal tubule changes in kidney tissue. Although these effects reversed in primates, the kidney safety signals were considered significant enough to halt further clinical development. This remains a major concern for any consideration of Adipotide use.

How much weight can Adipotide actually produce?

In obese rhesus macaques, 0.43mg/kg SC daily for 28 days produced 7.4-14.7% body weight loss with improved insulin sensitivity. However, primate studies don't guarantee equivalent human efficacy, and the kidney safety signals prevented human Phase 2 trials from determining real-world dose-response in people.

Can I combine Adipotide with semaglutide for enhanced weight loss?

No combination data exists, and stacking has theoretical risks. Both would drive rapid weight loss and dehydration. Adipotide shows dose-dependent kidney effects, and semaglutide users already face dehydration/GI issues. Combined use requires careful monitoring of renal function, electrolytes, and hydration status, best avoided without specialist supervision.

Adipotide

Dosing Summary

Dose
0.43 mg/kg
Frequency
Once daily
Cycle
28 days
Storage
Lyophilized: -20°C freezer. Reconstituted: 2-8°C refrigerated

Specifications

Purity≥98% (HPLC verified)
FormLyophilized powder
Packaging2mg / 5mg
StorageStore at -20°C, protect from light
Catalog No.AP2 / AP5

Research Data

4
Studies
2025
Latest
0
Recent

Available Sizes

2mg$27
5mg$37