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Reference

Peptide Glossary: 120 Terms in Pharmacology, Dosing, and Safety

Click any term for the anchor link. Use the category jump-bar to filter by topic. Educational only; not medical advice.

Six categories

  • Pharmacology: 25 terms (agonist, half-life, titration, etc.)
  • Dosing: 20 terms (mcg, mg, BID, QW, loading dose, etc.)
  • Reconstitution: 15 terms (bac water, U-100 syringe, lyophilized, etc.)
  • Safety: 25 terms (adverse event, CTCAE grading, MTC, MEN2, etc.)
  • Regulatory: 15 terms (FDA-approved, Phase 1-4, research compound, etc.)
  • Mechanism: 20 terms (GLP-1, GIP, GHRH, thymosin beta-4, etc.)

Pharmacology

25 terms in this category.

Agonist
A compound that binds to a receptor and activates it. Most peptide drugs are receptor agonists. Contrast antagonist.
Antagonist
A compound that binds to a receptor and blocks activation.
Partial agonist
A compound that binds and activates a receptor but with reduced maximal effect compared to a full agonist.
Inverse agonist
A compound that binds and produces the opposite biological effect of an agonist.
Receptor
A protein on or in a cell that recognizes a specific molecule and triggers a downstream signal.
GLP-1 receptor
The receptor activated by glucagon-like peptide-1 and by GLP-1 class drugs (semaglutide, tirzepatide, retatrutide).
Half-life
The time required for a compound's plasma concentration to fall by 50 percent. Semaglutide ~1 week, tirzepatide ~5 days, BPC-157 minutes.
Cmax
The peak plasma concentration of a compound after administration.
Tmax
The time after dosing at which Cmax is reached.
AUC
Area under the plasma concentration vs time curve. A measure of total drug exposure.
Bioavailability
The fraction of an administered dose that reaches systemic circulation unchanged.
First-pass metabolism
Hepatic metabolism that reduces oral drug bioavailability. Peptides are typically injected to bypass this.
Subcutaneous
Subcutaneous (subQ) injection delivers drug into the fatty layer just below the skin. The default route for most peptides.
Intramuscular
Intramuscular (IM) injection delivers drug into muscle tissue. Faster absorption than subQ.
Pharmacokinetics
Pharmacokinetics (PK) is the study of how a compound is absorbed, distributed, metabolized, and excreted.
Pharmacodynamics
Pharmacodynamics (PD) is the study of what a compound does to the body, including potency and effect duration.
Titration
Gradual dose escalation to minimize side effects. Standard for GLP-1 class drugs.
Steady state
The point at which drug input equals drug elimination, producing stable plasma levels. Typically reached after 4 to 5 half-lives.
Depot formation
Localized accumulation of injected drug that slowly releases over time, extending half-life.
Secretagogue
A compound that triggers release of an endogenous hormone. Ipamorelin is a GH secretagogue.
Analog
A structurally modified compound retaining the parent's core activity. Semaglutide is a GLP-1 analog.
Fragment
A truncated peptide retaining some activity of the parent. BPC-157 is a 15-amino-acid fragment of body protection compound.
kDa
Kilodalton, a molecular weight unit. Peptides are typically 1 to 5 kDa, proteins 10+ kDa.
Pulsatile
Pulsatile release means hormone is secreted in bursts (e.g., GH at night) rather than continuously.
Tachyphylaxis
Diminishing response to a drug after rapid repeated dosing. Mitigated by titration or cycling.

Dosing

20 terms in this category.

mcg
Microgram. 1,000 mcg = 1 mg. BPC-157 doses are usually 250 to 500 mcg.
mg
Milligram. 1 mg = 1,000 mcg. GH-axis peptides are usually 1 to 2 mg/day.
IU
International unit. A potency-based unit; conversion to mg varies by compound. Not interchangeable with syringe units.
U-100 syringe
A 100-unit insulin syringe. Each unit = 0.01 mL. The standard syringe for research peptide dosing.
U-40 syringe
A 40-unit insulin syringe (less common). Each unit = 0.025 mL.
U-500 syringe
A 500-unit syringe used for concentrated insulin. Not standard for peptide dosing.
Units
Syringe markings. Not interchangeable with IU. With a U-100 syringe, 1 unit = 0.01 mL of solution.
BID
Twice daily (bis in die). BPC-157 dosing is often BID.
QD
Once daily (quaque die). GHK-Cu is typically QD.
TIW
Three times weekly. CJC-1295/Ipamorelin sometimes dosed TIW.
QW
Once weekly. GLP-1 class drugs are typically QW.
Loading dose
A higher initial dose used to rapidly reach therapeutic concentrations. TB-500 protocols often use loading.
Maintenance dose
The ongoing lower dose used after loading or after titration is complete.
Titration ladder
A defined sequence of increasing weekly doses, used for GLP-1 class drugs to minimize GI side effects.
Cycle
A defined period of consecutive dosing followed by a break. Research compounds often cycled 4 to 8 weeks on, 4 to 8 weeks off.
On-cycle
Active dosing period.
Off-cycle
Rest period during which the compound is not administered.
Weeks per vial
A calculation: vial mg divided by weekly dose mg. Drives cost per month.
ED50
The dose producing 50 percent of maximal effect.
ED90
The dose producing 90 percent of maximal effect.

Reconstitution

15 terms in this category.

Bacteriostatic water
Bacteriostatic water for injection. Sterile water containing 0.9 percent benzyl alcohol as a preservative. Standard diluent for multi-use peptide vials.
Benzyl alcohol
The preservative in bacteriostatic water. Inhibits bacterial growth in multi-use vials.
Vial
A small glass bottle with a rubber stopper, sealed under vacuum. Most peptides ship as a lyophilized powder in vials.
Diluent
The liquid used to dissolve a lyophilized peptide. Bacteriostatic water is the standard diluent.
Reconstitution
The process of dissolving a lyophilized peptide in bacteriostatic water to create an injectable solution.
Swirl
Gentle agitation method used to mix peptide powder with diluent. Peptides should be swirled, not shaken, to preserve structure.
Recon volume
The volume of bacteriostatic water added to a vial. Determines concentration and units-per-vial math.
Units per vial
Calculated as (vial mg / dose per unit). With a 20 mg vial in 2 mL bac water, units-per-vial = 200.
27G needle
27-gauge syringe needle. Common for subQ peptide injection.
29G needle
29-gauge needle. Thinner than 27G; reduces injection-site discomfort.
31G needle
31-gauge needle. Among the thinnest available. Standard for insulin and increasingly for peptides.
Insulin syringe
A small-volume syringe (typically 0.3 to 1 mL) marked in U-100 units. Standard for research peptide dosing.
0.5 mL syringe
A 0.5 mL insulin syringe. Holds up to 50 units of solution.
1 mL syringe
A 1 mL insulin syringe. Holds up to 100 units of solution.
Lyophilized
Freeze-dried. Most peptide vials ship as a lyophilized powder cake that requires reconstitution.

Safety

25 terms in this category.

Adverse event
Adverse event (AE). Any unfavorable medical occurrence during drug use, whether causally related or not.
Serious adverse event
Serious adverse event (SAE). An AE that results in death, hospitalization, persistent disability, or is life-threatening.
CTCAE grading
Common Terminology Criteria for Adverse Events. A 5-grade severity scale (Grade 1 mild to Grade 5 death) used in oncology and increasingly in peptide trials.
Contraindication
A condition or factor that makes a drug inappropriate to use.
Absolute contraindication
A condition under which a drug must never be used. Example: Wilson disease for GHK-Cu.
Relative contraindication
A condition under which a drug should be used with caution or monitoring.
Black-box warning
The FDA's strongest prescription drug label warning. Tirzepatide and semaglutide both carry one for thyroid C-cell tumors.
Nausea
The reported adverse event with the highest incidence on GLP-1 class drugs (around 30 percent in Phase 3 trials).
Emesis
Vomiting. A frequent GI adverse event on GLP-1 class drugs.
Lipohypertrophy
Localized accumulation of fat at repeated injection sites. Mitigated by site rotation.
Injection-site reaction
Localized redness, itching, swelling, or pain at the injection site. The most common adverse event for non-GLP-1 research peptides.
Erythema
Redness of the skin, often at an injection site.
Pruritus
Itching, often at an injection site or as part of a systemic reaction.
Hypoglycemia
Low blood glucose. A risk on GLP-1 class drugs especially when combined with insulin or sulfonylureas.
Hyperglycemia
Elevated blood glucose.
Pancreatitis
Inflammation of the pancreas. A rare reported adverse event on GLP-1 class drugs.
Gastroparesis
Delayed gastric emptying. Reported with semaglutide, less common with tirzepatide.
MTC
Medullary thyroid carcinoma. A rare thyroid cancer linked to C-cell tumors. Black-box concern for GLP-1 class drugs.
MEN2
Multiple endocrine neoplasia type 2. A hereditary syndrome that includes risk of MTC. Absolute contraindication for tirzepatide and retatrutide.
Retinopathy
Damage to the retinal blood vessels. Risk in diabetics on GH-axis peptides; semaglutide also carries a documented retinopathy signal in SUSTAIN-6.
IGF-1
Insulin-like growth factor 1. Downstream marker of GH-axis activity. Elevated levels are monitored on CJC-1295/Ipamorelin protocols.
Water retention
Edema. A common reported effect on GH-axis peptides, typically transient.
Wilson disease
A genetic disorder of copper metabolism. Absolute contraindication for GHK-Cu and any copper-containing peptide.
Angiogenesis
Formation of new blood vessels. Pro-angiogenic activity in tissue-repair peptides raises a theoretical (not human-confirmed) tumor concern.
Pharmacovigilance
Ongoing safety monitoring of a drug after release. FDA-approved drugs report through MedWatch; research compounds rely on user-reported registries.

Regulatory

15 terms in this category.

FDA-approved
Cleared by the US Food and Drug Administration for a specific indication after Phase 3 trials. Examples: Mounjaro (tirzepatide), Ozempic (semaglutide).
Phase 1
First-in-human safety trials, typically n=20 to 100, healthy volunteers.
Phase 2
Dose-finding and efficacy trials, typically n=100 to 500, target population.
Phase 3
Pivotal efficacy and safety trials, typically n=1,000 to 10,000+. Required for FDA approval.
Phase 4
Post-marketing surveillance after a drug is approved.
IND
Investigational New Drug application. The FDA submission required to begin human trials.
NDA
New Drug Application. The FDA submission required for marketing approval.
503A
A US compounding pharmacy that prepares patient-specific compounded drugs. Was the source of compounded semaglutide during shortages.
503B
A US outsourcing facility that prepares larger-batch compounded drugs.
Research compound
A peptide intended for laboratory research only and not approved for human consumption. BPC-157, TB-500, KLOW Combo, MOTS-c, SLU-PP-332, and others fall in this category.
Prescription
Drugs that require a licensed prescriber's authorization. All FDA-approved peptides are prescription only.
COA
Certificate of Analysis. A document from an independent lab confirming the purity and identity of a peptide batch. Peptara publishes COAs on request.
HPLC
High-performance liquid chromatography. The standard purity test for peptides.
Mass spectrometry
Mass spectrometry. Confirms peptide identity by measuring molecular weight.
NMR
Nuclear magnetic resonance. Confirms peptide structure.

Mechanism

20 terms in this category.

GLP-1
Glucagon-like peptide-1. An endogenous incretin hormone that triggers insulin release, slows gastric emptying, and reduces appetite.
GIP
Glucose-dependent insulinotropic polypeptide. The second incretin hormone. Tirzepatide and retatrutide activate the GIP receptor in addition to GLP-1.
Glucagon
A pancreatic hormone that raises blood glucose. Retatrutide is a glucagon receptor agonist in addition to GLP-1 and GIP.
GH
Growth hormone. The pituitary hormone targeted indirectly by GH-axis peptides.
GHRH
Growth-hormone-releasing hormone. A hypothalamic peptide that triggers GH release. CJC-1295 is a GHRH analog.
GHRP
Growth-hormone-releasing peptide. A class of synthetic peptides that mimic ghrelin to trigger pulsatile GH release. Ipamorelin is a GHRP.
mTOR
Mechanistic target of rapamycin. A central regulator of cell growth and metabolism. Inhibition is linked to longevity research.
AMPK
AMP-activated protein kinase. A cellular energy sensor activated by exercise and by some peptides (notably MOTS-c).
Mitochondrial biogenesis
The formation of new mitochondria within cells. Driven by MOTS-c, exercise, and some pharmacological agents.
Thymosin beta-4
A 43-amino-acid peptide involved in actin sequestration, angiogenesis, and tissue repair. TB-500 is a synthetic fragment of thymosin beta-4.
BPC
Body Protection Compound. A 15-amino-acid peptide derived from human gastric juice, studied for tissue repair and gut healing.
Copper peptide
A peptide complexed with a copper ion. GHK-Cu is the canonical copper peptide used for skin and wound healing.
KPV
Lys-Pro-Val. A tripeptide with anti-inflammatory activity, included in the KLOW Combo blend.
Melanocortin
A class of peptide hormones (alpha-MSH, ACTH) that activate melanocortin receptors. PT-141 (bremelanotide) and MT-2 (melanotan-2) are melanocortin agonists.
BDNF
Brain-derived neurotrophic factor. A neuroplasticity protein elevated by some nootropic peptides (e.g., Semax).
VEGF
Vascular endothelial growth factor. A pro-angiogenic signaling protein upregulated by some tissue-repair peptides.
Nitric oxide
A vasodilatory signaling molecule involved in BPC-157's pro-angiogenic activity and in some vasodilator peptide effects.
Collagen synthesis
The cellular process of producing collagen. Upregulated by GHK-Cu and to a lesser extent by BPC-157.
Fibroblast
A connective-tissue cell that produces collagen and other extracellular matrix proteins. Targeted by GHK-Cu.
Incretin
A class of hormones (GLP-1, GIP) that trigger insulin release in response to nutrients. The GLP-1 class drug family is built on incretin biology.
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