HGH Fragment 176-191
Also known as: HGH Frag 176-191
A synthetic C-terminal fragment of human growth hormone claimed to stimulate adipocyte lipolysis without binding the GH receptor or raising IGF-1, though human fat-loss evidence is weak.
- Drug class
- Growth hormone C-terminal lipolytic fragment
- Primary targets
- Adipocyte lipid metabolism
- Dose reference
- No established human dose; research-only
- Half-life
- Very short (minutes); poorly characterized
- Developer / origin
- Ng et al. (Monash University)
- Reference year
- 1994
- Evidence score
- 2/5 - Weak
Weak
Animal and isolated-tissue studies show the hGH 176-191 domain stimulates lipolysis without GH's IGF-1 effects, but there is no convincing controlled human fat-loss evidence; its optimized analog AOD-9604 failed a human obesity trial.
Mostly animal, ex vivo, cell, or indirect evidence.
Evidence basis
- Synthetic hGH 177-191 reduced adipose mass and lipogenesis in obese mice
- Stimulated hormone-sensitive lipase without binding the GH receptor
- No controlled human fat-loss trial for the unmodified fragment
- Optimized analog AOD-9604 failed human obesity development
How to read this entry
Dose references and half-life values are pulled from trial protocols, labels, reviews, or published summaries where available. They are context for research and comparison, not a personal dosing recommendation.
Status matters: approved drugs have regulated indications; investigational compounds are still being studied; research-only peptides do not have established human dosing, safety, or efficacy for consumer use.
HGH Fragment 176-191 guides
Read the matching guide or adjacent research pages for more context.
Peptide calculators
Use calculators for concentration, unit conversion and repeated-dose accumulation math.
Compare with related peptides
Stay inside the same research category and compare mechanism, status and evidence quality.
Retatrutide
LY3437943
Activates GLP-1, GIP and glucagon receptors simultaneously to suppress appetite and raise energy expenditure.
Tirzepatide
LY3298176, Mounjaro, Zepbound
Activates GLP-1 and GIP receptors to improve glycemic control and reduce appetite + body weight.
Semaglutide
Ozempic, Wegovy, Rybelsus
Mimics the incretin GLP-1, slowing gastric emptying and reducing appetite while improving insulin secretion.
Liraglutide
Victoza, Saxenda
Daily GLP-1 analog. Reduces appetite and improves glycemic control via the same incretin pathway as semaglutide.
Category hub
Open the category page for the full comparison table and FAQ.