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GLOSSARY · 36 TERMS

Peptide glossary

The vocabulary you need to read a peptide page without guessing — receptors, evidence terms, measurement units and the differences that matter most.

Agonist
A molecule that binds a receptor and activates it, producing the same kind of signal the body's own messenger would. GLP-1 receptor agonists are drugs shaped closely enough to GLP-1 to switch its receptor on.
Amylin analogue
A synthetic version of amylin, a hormone co-secreted with insulin that slows gastric emptying and signals satiety. Cagrilintide is the analogue most often paired with GLP-1 agonists in trials.
Antagonist
A molecule that binds a receptor and blocks it rather than activating it, preventing the natural messenger from signalling.
Bacteriostatic waterBAC water
Sterile water containing roughly 0.9% benzyl alcohol as a preservative, which inhibits bacterial growth so a multi-dose vial can be entered more than once. Distinct from sterile water for injection, which has no preservative. Benzyl alcohol preparations are contraindicated in neonates under FDA labelling.
Bioavailability
The fraction of an administered amount that reaches the bloodstream unchanged. Injected peptides are near-complete; oral peptides are typically a fraction of one percent without an absorption enhancer.
Concentration
How much drug sits in each millilitre of solution, written mg/mL or mcg/mL. After reconstitution it equals the vial's mass divided by the diluent volume added.
Diluent
The liquid added to a lyophilised (freeze-dried) vial to dissolve its contents. Bacteriostatic water and sterile water for injection are the two common diluents.
DPP-4Dipeptidyl peptidase-4
An enzyme that rapidly degrades native GLP-1 and GIP, giving natural GLP-1 a half-life of a couple of minutes. Long-acting analogues are engineered to resist it.
Dual agonist
A single molecule that activates two receptors. Tirzepatide, a GIP and GLP-1 receptor agonist, is the best-known example.
Endotoxin
Bacterial cell-wall fragments that cause fever and inflammation even when no live bacteria remain. Pharmaceutical manufacturing tests for them; research-grade material frequently does not.
Excipient
A non-active ingredient in a vial — buffer, bulking agent, stabiliser — present to protect or dissolve the active compound.
GHSGrowth hormone secretagogue
A compound that prompts the pituitary to release its own growth hormone rather than supplying growth hormone directly. Includes GHRH analogues such as sermorelin and tesamorelin, and ghrelin-receptor agonists such as ipamorelin and hexarelin.
GIPGlucose-dependent insulinotropic polypeptide
An incretin hormone released from the upper small intestine after eating. Adding GIP receptor activity to GLP-1 activity is the basis of tirzepatide.
GLP-1Glucagon-like peptide-1
An incretin hormone cleaved from proglucagon in the gut that amplifies glucose-dependent insulin release, suppresses glucagon, slows gastric emptying and reduces appetite through central pathways.
GLP-2Glucagon-like peptide-2
A sibling peptide from the same proglucagon precursor that acts on a different receptor to promote intestinal growth and absorption. Its analogues treat short bowel syndrome, not obesity.
GLP-3
Not a real hormone or receptor. An informal online nickname for retatrutide, an investigational triple agonist of the GLP-1, GIP and glucagon receptors.
Glucagon receptor
The receptor for glucagon, chiefly on liver cells. Activating it raises hepatic glucose output and energy expenditure and mobilises liver fat, which is why it is included in triple agonists.
Half-life
The time for the amount of drug in the body to fall by half. It sets how often a compound would need to be given to maintain exposure, and how long it lingers after stopping.
Incretin
A gut hormone released in response to food that increases insulin secretion more than the same glucose given intravenously would. GLP-1 and GIP are the two human incretins.
IUInternational unit
A measure of biological activity, defined separately for each substance against a WHO reference standard. IU is not a mass and never converts to milligrams by a universal factor — and it is not the same thing as the 'units' printed on an insulin syringe.
Lyophilised
Freeze-dried. Peptides are usually supplied as a lyophilised powder or cake because they are far more stable dry than in solution.
Melanocortin receptor
A family of receptors (MC1R through MC5R) involved in pigmentation, appetite, inflammation and sexual arousal. Targeted by peptides such as bremelanotide and melanotan II.
Peptide
A short chain of amino acids — conventionally up to around fifty — joined by peptide bonds. Longer chains are called proteins. Most peptides are digested if swallowed, which is why they are typically injected.
PharmacodynamicsPD
What the drug does to the body: which receptors it hits and what effect follows.
PharmacokineticsPK
What the body does to the drug: absorption, distribution, metabolism and elimination, summarised in figures like half-life and peak concentration.
Phase 1 / 2 / 3
Stages of human trials. Phase 1 tests safety and pharmacokinetics in a small group; phase 2 tests activity and dose-finding; phase 3 tests efficacy and safety at scale against a comparator. Approval normally follows successful phase 3.
Placebo-subtracted
A result reported after removing the change seen in the placebo arm, isolating the effect attributable to the drug rather than to trial participation and lifestyle support.
Proglucagon
The precursor protein that is cleaved differently in the pancreas and gut to yield glucagon, GLP-1, GLP-2 and other fragments.
Receptor
A protein on or in a cell that a signalling molecule binds to, triggering a response inside the cell. Which receptors a peptide binds is the single most useful fact about it.
Reconstitution
Dissolving a lyophilised powder by adding a measured volume of diluent. It changes concentration, never the total amount of drug in the vial.
Research chemical
Material sold for laboratory use only. It is not manufactured, tested or released to pharmaceutical standards, and identity, purity, endotoxin load and sterility are frequently unverified.
SubcutaneousSC / SubQ
Into the fat layer beneath the skin — the usual route for peptide injections, giving slower, steadier absorption than intramuscular or intravenous routes.
Syringe units
The numbers printed on an insulin syringe barrel. They are volume markings tied to insulin concentration: on a U-100 syringe, 100 units equal 1 mL, so one unit is 0.01 mL. They are not IU of a peptide and not milligrams.
Titration
Stepwise adjustment of an amount over time, used clinically to improve tolerability. GLPWiki does not publish titration schedules.
Triple agonist
A molecule that activates three receptors at once. Retatrutide targets the GLP-1, GIP and glucagon receptors and remains investigational.
U-100 / U-50 / U-40
Insulin syringe scales. The number is units per millilitre: a U-100 syringe reads 100 units to the millilitre, U-50 reads 50, U-40 reads 40. Using the wrong scale changes what a given mark means.

EDUCATIONAL REFERENCE ONLY · Not medical advice. Nothing here diagnoses, treats, cures or prevents any disease, and nothing here is a dosing recommendation. Consult a licensed clinician before any treatment decision.