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34 PEPTIDES · 12 CLASSES · 43 SOURCES

GLPWikiThe encyclopedia of peptides

Incretins and the triple agonists people call GLP-3, plus repair peptides, growth-hormone secretagogues, melanocortins and the rest of the field. Every entry states the mechanism, the receptor targets, the evidence, and where it came from.

GLPWiki is an independent, citation-first educational reference. It sells nothing, links to no suppliers, carries no sponsored entries, and publishes no doses or protocols. It explains what a compound is and what has been measured — it is not medical advice.

DATASHEET · RETATRUTIDE
Also called
GLP-3
Receptors
GLP-1 + GIP + glucagon
Half-life
~6 days
Status
Phase 3

GLP-3 is not a hormone or a receptor. It is a nickname for retatrutide, an investigational Eli Lilly triple agonist. Not approved by any regulator.

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Featured peptides

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GLP-3Phase 3

Retatrutide

An investigational triple agonist widely nicknamed "GLP-3" online. There is no GLP-3 hormone or receptor — the name is a consumer shorthand for a molecule that hits three receptors at once.

Half-life ~6 daysRead →
GLP-1Approved

Semaglutide

A once-weekly GLP-1 receptor agonist and the most widely prescribed drug in the class. Approved for type 2 diabetes, chronic weight management and cardiovascular risk reduction.

Half-life ~7 daysRead →
DUAL AGONISTApproved

Tirzepatide

The first approved dual incretin agonist, activating both the GIP and GLP-1 receptors. Approved for type 2 diabetes, chronic weight management and obstructive sleep apnoea in obesity.

Half-life ~5 daysRead →
COMMON QUESTIONS

What people ask first

Is GLP-3 a real hormone?
No. There is no GLP-3 hormone or receptor. It is an informal nickname used online for retatrutide, an investigational triple agonist that activates the GLP-1, GIP and glucagon receptors at once.
What is the difference between GLP-1 and GLP-2?
Both are cleaved from the same proglucagon precursor, but they act on different receptors. GLP-1 drives insulin secretion and satiety; GLP-2 drives intestinal growth and absorption and is used in short bowel syndrome, not weight management.
Why do dual and triple agonists produce more weight loss?
Adding GIP and glucagon receptor activity recruits pathways GLP-1 alone does not reach — GIP appears to improve tolerability and adipose handling, while glucagon raises energy expenditure and mobilises hepatic fat.
Where does the information here come from?
Every entry cites primary sources: peer-reviewed trial publications and trial registry records. Figures are trial means under protocol conditions, not predictions for any individual.