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Reference

Peptide glossary

Every term you'll hit researching peptides, defined in plain English. No jargon wall, no medical-textbook density. If a guide or entry uses a word you don't know, it's probably here.

Dosing & units

mcg
Microgram, the standard dose unit for most peptides. 1 milligram (mg) equals 1,000 micrograms (mcg). When a protocol says '250 mcg', that's 0.25 mg. Most peptide vials are dosed in mg total, but doses-per-injection are usually in mcg.
mg
Milligram. The unit your peptide vial size is usually labeled in (e.g., 'BPC-157 5mg vial'). Doses are typically a fraction of that, expressed in mcg.

Injection & delivery

BAC water
Bacteriostatic water. Sterile water mixed with 0.9% benzyl alcohol that prevents bacterial growth, letting you reuse the vial across multiple doses without contamination. This is what you mix lyophilized (freeze-dried) peptide powder with to reconstitute it.
IM
Intramuscular injection. Deeper than sub-q, into the muscle tissue. Less common for peptides, more common for hormones. Uses a longer needle. TB-500 is sometimes given IM.
Insulin syringe
Standard insulin syringe. 1mL barrel total volume, marked in 100 'units' instead of mL, so 0.5mL = 50 units. The needle is 29-31 gauge, very thin, designed for sub-q injection. The Calculator converts your peptide dose into exact units to draw.
Lyophilized
Freeze-dried. The peptide is shipped as a fluffy white powder in a sealed vial, stable for months in the fridge or years in the freezer. To use it, you reconstitute (mix) with bacteriostatic water.
Reconstitution
The process of mixing a lyophilized peptide vial with bacteriostatic water so it becomes liquid and injectable. Done once per vial. See the Reconstitution guide for the step-by-step.
Sub-q
Subcutaneous injection. The needle goes into the fat layer just under the skin, not into muscle. Most peptides are sub-q. Common sites: lower abdomen (2 inches from the navel), love handles, outer thigh. Use a 29-31 gauge insulin syringe.

Scheduling & cycling

Cycle
A defined on-period of dosing (e.g., 8 weeks) followed by an off-period (e.g., 4 weeks). Why: your receptors downregulate over time when constantly stimulated, so the same dose stops working. The break lets receptors upregulate back to baseline.
EOD
Every other day. A common dosing frequency. Mon/Wed/Fri/Sun/Tue, etc. Used when daily would over-saturate the receptor or when the half-life is long enough to skip days.
Loading phase
The opening 1-3 weeks of a cycle where doses are higher or more frequent than maintenance. Used to push tissue concentrations up faster. TB-500 and MT-1/2 are the classic examples.
Maintenance phase
The phase after loading where doses drop to a lower frequency or amount. Goal: hold the effect with less product and fewer side effects.
Titration
Step-up dosing. Common with GLP/GIP class drugs (semaglutide, tirzepatide, retatrutide). You start at the lowest dose, hold it for 4 weeks, then increase if tolerated. Skipping titration spikes side effects badly.

Biology & mechanisms

Agonist
A molecule that binds a receptor and activates it, switching on the downstream effect. Most peptides in this catalog are agonists: a GLP-1 agonist turns on the GLP-1 receptor; a melanocortin agonist turns on pigment and libido receptors. The opposite is an antagonist, which blocks the receptor instead.
Amylin
A hormone secreted alongside insulin that slows gastric emptying and signals fullness through a separate pathway from GLP-1. Amylin analogs (Cagrilintide, Pramlintide) pair naturally with GLP-1 drugs, which is the whole idea behind CagriSema.
Analog
A synthetic molecule modeled on a natural one with small changes to improve it, usually a longer half-life or stronger receptor binding. Semaglutide is a GLP-1 analog; Tesamorelin is a GHRH analog. Those tweaks are what let a once-weekly shot replace a hormone your body would otherwise clear in minutes.
Boxed warning
Formerly called a 'black-box warning,' the most serious warning the FDA places on a prescription label, reserved for risks that can be serious or life-threatening. Worth knowing which of your compounds carry one and which don't; labels change over time as evidence accumulates (several peptides had warnings removed years after approval).
Contraindication
A specific situation or pre-existing condition under which you should not use a compound because the risk is too high (for example, a personal or family history of medullary thyroid cancer with GLP-1 drugs). Different from a side effect: a contraindication is a reason not to start at all.
DAC
Drug Affinity Complex. A modification that binds the peptide to albumin in your blood, dramatically extending half-life (CJC-1295 with DAC = ~8-day half-life vs ~30 min without). The 'no-DAC' version of CJC-1295 is the short-acting one used in peptide stacks.
Dual / triple agonist
A single peptide built to activate two (dual) or three (triple) receptors at once. Tirzepatide is a dual GLP-1 + GIP agonist; Retatrutide is a triple GLP-1 + GIP + glucagon agonist. Each added receptor tends to add weight-loss effect, which is why the triple agonists post the largest trial numbers so far.
GHRH
Growth-hormone-releasing hormone, the brain signal that tells your pituitary to release growth hormone. GHRH analogs (Sermorelin, CJC-1295, Tesamorelin) mimic that signal, which is why they're paired with a secretagogue like Ipamorelin for a bigger, cleaner GH pulse.
GIP
Glucose-dependent insulinotropic polypeptide. A second appetite/insulin-related receptor. Adding GIP activation to GLP-1 (as Tirzepatide does) gives stronger weight-loss effect than GLP-1 alone.
GLP-1
Glucagon-like peptide-1. A natural hormone your gut releases after eating that signals satiety to your brain. The 'GLP-1 drugs' (semaglutide, liraglutide) mimic and prolong this signal, suppressing appetite and slowing gastric emptying.
Half-life
The time it takes for half of a dose to be metabolized and cleared. Drives how often you dose. A 4-hour half-life peptide needs daily or twice-daily dosing; a 6-day half-life peptide is comfortably weekly. Steady-state (your level stops rising) is reached around 4-5 half-lives in.
IGF-1
Insulin-like growth factor 1. The downstream hormone produced by your liver when GH hits it. Most GH effects are actually IGF-1 effects. Lab measurement of IGF-1 is the standard way to verify a GH-axis peptide is working.
Receptor downregulation
When you stimulate a receptor too much for too long, your cells reduce the number of receptors or their sensitivity to compensate. This is why peptides need cycle breaks, your body adapts to the signal.
Secretagogue
A compound that prompts a gland to secrete more of a hormone it already makes, instead of supplying the hormone directly. GH secretagogues (Ipamorelin, MK-677, CJC-1295) nudge your pituitary to release your own growth hormone, which is why they preserve the natural pulse rather than flatlining it the way injected HGH can.

Sourcing & vendors

Vial
The sealed glass bottle that ships from the vendor with peptide powder inside. Has a rubber septum top. You inject BAC water through the septum to reconstitute, then draw doses through the same septum.

Want the full picture?

The peptide index breaks down every compound with dose ranges, timelines, and side effects. The reconstitution calculator turns vial size plus BAC water into the exact units to draw.