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.
Next steps
Side effects reference
Cross-reference: research-frame safety reference for 8 compounds with citations. Glossary terms link directly into this page.
Open reference
Reconstitution guide
4-step method plus units-not-mL calculator. Required reading before any research-vial protocol.
Open guide
FAQ
Frequently asked questions about ordering, shipping, peptide use, and protocols.
Open FAQ
Educational only. Not medical advice. Glossary definitions are aggregated from peer-reviewed literature, trial registries, and FDA labeling. Consult a qualified healthcare provider before any peptide use.