Metabolic & Weight Loss Peptides
Explore metabolic profiles and evidence guides by mechanism, research stage, safety context, and primary sources.
Research area
How to use this hub
Category membership organizes related research questions. It does not establish effectiveness, approval, or suitability for a person.
Evidence boundary
Approved products, investigational analogs, compounded formulations, and preclinical metabolic mechanisms do not share the same evidence or regulatory status.
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Build context before interpreting an individual profile.
GLP-1 agonist comparison
Compare targets, trial phases, outcomes, safety, and approval status.
Read guideWhat is GLP-1?
Review incretin physiology, receptor effects, medicines, and evidence boundaries.
Read guideTesamorelin vs sermorelin
Compare mechanism, evidence, approved context, and common claim confusion.
Read guideProfiles in this research area
Open a profile for its mechanism, evidence stage, safety context, and linked references.
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Read the full category research notes
These notes map terminology and research themes. Verify claims in the linked profile references and current primary records.
Metabolic & Weight Loss Peptides
This category covers peptides researched for their effects on body weight, appetite regulation, glucose metabolism, and fat oxidation. The GLP-1 receptor agonists represent the most clinically advanced class, while other peptides target fat metabolism through distinct mechanisms.
Complete Peptide Directory
GLP-1 Receptor Agonists
| Peptide | Description | Primary Mechanism |
|---|---|---|
| Semaglutide | Long-acting GLP-1 agonist with strongest weight loss efficacy; FDA-approved | GLP-1R agonist; reduces appetite, slows gastric emptying, improves glycemia |
| Semaglutide Oral | Oral formulation of semaglutide using SNAC absorption enhancer (Rybelsus) | Same GLP-1R mechanism with oral bioavailability via SNAC co-formulation |
| Liraglutide | Daily GLP-1 agonist for type 2 diabetes and obesity; FDA-approved | GLP-1R agonist; glucose homeostasis, appetite regulation, neuroprotection |
| Tirzepatide | Dual GIP/GLP-1 receptor agonist with superior weight loss outcomes | Dual incretin agonism; synergistic metabolic effects from two pathways |
| Retatrutide | Triple agonist targeting GLP-1, GIP, and glucagon receptors simultaneously | Triple incretin signaling for maximum metabolic impact |
| Survodutide | Dual GLP-1/glucagon receptor agonist for obesity and NASH | GLP-1 appetite suppression plus glucagon-driven energy expenditure |
| Mazdutide | Dual GLP-1/glucagon receptor agonist in clinical development | Dual agonism for weight loss and metabolic disease |
| Pemvidutide | Dual GLP-1/glucagon receptor agonist targeting NASH and obesity | Liver-targeted metabolic effects alongside weight reduction |
| Orforglipron | Non-peptide oral GLP-1R agonist in Phase 3 trials | Small-molecule GLP-1R agonist; high oral bioavailability |
| Danuglipron | Non-peptide oral GLP-1R agonist from Pfizer | Small-molecule GLP-1R agonist; twice-daily oral dosing |
| Ecnoglutide | Long-acting GLP-1R agonist with biased agonism profile | GLP-1R signaling with reduced GI side effects through biased agonism |
| Maritide | Long-acting amylin/GLP-1 receptor co-agonist (monthly dosing) | Dual amylin and GLP-1 signaling for sustained appetite suppression |
| Cagrilintide | Long-acting amylin analog studied alongside semaglutide | Amylin receptor agonist; complementary appetite reduction with GLP-1 |
Appetite & Satiety Hormones
| Peptide | Description | Primary Mechanism |
|---|---|---|
| GLP-1 | Endogenous incretin hormone that regulates glucose and appetite | GLP-1 receptor activation; reference compound for GLP-1 agonist drugs |
| GLP-2 | Intestinal growth factor that promotes gut mucosal repair | GLP-2 receptor; intestinal epithelial proliferation; short bowel syndrome |
| GIP | Glucose-dependent insulinotropic polypeptide (gastric inhibitory peptide) | GIP receptor; insulin secretion; fat metabolism; bone health |
| Peptide YY | Gut hormone released postprandially that suppresses appetite | Y2 receptor agonist; reduces food intake; slows gastric emptying |
| Amylin | Pancreatic hormone co-secreted with insulin that promotes satiety | Amylin receptor; slows gastric emptying; suppresses glucagon |
| Cholecystokinin | Gut peptide that signals meal-related satiety | CCK receptors; gallbladder contraction; pancreatic enzyme secretion |
| Glucagon | Pancreatic hormone that mobilizes glucose and increases energy expenditure | Glucagon receptor; glycogenolysis; gluconeogenesis; thermogenesis |
| Lac-Phe | Exercise-induced metabolite (lactate-phenylalanine) that suppresses appetite | Post-exercise appetite regulation; metabolic signaling |
Melanocortin & Other Pathways
| Peptide | Description | Primary Mechanism |
|---|---|---|
| Setmelanotide | MC4R agonist for genetic obesity disorders; FDA-approved | Melanocortin-4 receptor agonist; targets hypothalamic appetite circuits |
| AOD-9604 | Stabilized HGH fragment analog for fat metabolism | Lipolytic fragment of GH; fat burning without growth-promoting effects |
| Adipotide (FTPP) | Peptide that targets blood vessels in adipose tissue | Induces apoptosis in adipose vasculature; targeted fat reduction |
Common Research Themes
GLP-1 Pathway: Semaglutide and Liraglutide both act on the GLP-1 receptor but differ in pharmacokinetics. The field is advancing toward dual (tirzepatide) and triple (retatrutide) agonists for enhanced efficacy.
Oral Metabolic Agents: Orforglipron, Danuglipron, and Semaglutide Oral represent the push toward oral alternatives to injectable GLP-1 agonists, with small-molecule mimetics bypassing peptide bioavailability challenges.
Amylin Co-agonism: Cagrilintide and Maritide leverage amylin signaling alongside GLP-1 for complementary appetite suppression through distinct brain regions.
Lipolysis vs. Adipose Targeting: AOD-9604 enhances fat breakdown (lipolysis) systemically, while Adipotide takes a different approach by cutting off blood supply specifically to fat tissue.
Getting Started
If you are new to this category, we recommend starting with Semaglutide — an FDA-approved GLP-1 receptor agonist with the strongest clinical evidence for weight management. From there, explore related peptides through the See Also sections on each page to build a comprehensive understanding of the research landscape.
Cognitive & Neuroprotective Peptides
Research peptides studied for cognitive enhancement, neuroprotection, anxiolytic effects, and neurological recovery.
Immune System Peptides
Research peptides that modulate immune function, enhance T-cell activity, reduce inflammation, and support antimicrobial defense.