Reference

Peptide Research Glossary

Definitions for common terms used in peptide research, dosing, and reconstitution. Browse alphabetically or search by topic.

A

A01

Acetic acid (0.6%)

Used to reconstitute IGF-1 LR3 and some other peptides. The acidic environment stabilises the peptide structure. Must be diluted with bacteriostatic water before injection.

A02

Acromegaly

Condition caused by excess growth hormone after growth plate closure. Relevant as an upper-limit reference for GH safety.

A03

Amide bond / Amidation

C-terminal modification in some peptides (e.g CJC-1295) that improves stability against proteolysis.

A04

Angiogenesis

Formation of new blood vessels. BPC-157 promotes angiogenesis via VEGF modulation — key part of its healing mechanism.

B

B01

BAC water (Bacteriostatic water)

Sterile water containing 0.9% benzyl alcohol, which inhibits bacterial growth. Allows multiple draws from one vial over several weeks. Standard reconstitution solvent for most research peptides.

B02

BDNF (Brain-Derived Neurotrophic Factor)

Protein supporting neuron survival and growth. Semax increases BDNF expression — considered part of its cognitive mechanism.

B03

Bioavailability (subcutaneous)

Absorption of a peptide injected subcutaneously. Most research peptides have SC bioavailability of 60–90%, depending on molecular weight.

B04

BPC-157

Body Protection Compound-157. Pentadecapeptide derived from a gastric protein. No human clinical trials — all evidence from rodent models.

C

C01

cAMP (Cyclic AMP)

Intracellular signalling molecule. GHRH receptor activation triggers cAMP production, stimulating GH synthesis and release.

C02

CJC-1295

Modified GHRH analogue. "No DAC" version has ~30-minute half-life; "with DAC" (Drug Affinity Complex) extends half-life to 7–10 days by binding to albumin.

C03

Concentration (mcg/ml or mg/ml)

The amount of peptide dissolved per millilitre of solvent. Calculated as: Vial mass ÷ Reconstitution volume.

D

D01

DAC (Drug Affinity Complex)

A lysine-maleimide modification on CJC-1295 that covalently binds to circulating albumin, dramatically extending half-life from ~30 min to 7–10 days.

E

E01

Epithalon

Tetrapeptide (Ala-Glu-Asp-Gly) developed by Vladimir Khavinson. Claimed to regulate telomerase activity. Fixed 10 mg/day × 10-day cycles based on Russian clinical protocols.

F

F01

Frequency (injection)

How often a peptide is administered. Expressed as injections per day or per week. Determines total vial consumption and days supply.

F02

Freeze-drying (lyophilization)

Process that removes water from peptides under vacuum to create a stable powder (lyophilisate). Allows long-term storage at room temperature before reconstitution.

G

G01

GH (Growth Hormone / Somatotropin)

Protein hormone released by the pituitary. Stimulates IGF-1 production. Declines ~14% per decade after age 30.

G02

GHRH (Growth Hormone-Releasing Hormone)

Hypothalamic peptide that stimulates GH synthesis and release from the pituitary. CJC-1295 and Sermorelin are GHRH analogues.

G03

GHRP (Growth Hormone-Releasing Peptide)

Class of synthetic peptides (Ipamorelin, GHRP-2, GHRP-6) that trigger GH release via ghrelin receptor (GHSR) activation. Mechanism independent of GHRH.

G04

GIP (Glucose-dependent Insulinotropic Polypeptide)

Incretin hormone. Tirzepatide is a dual GIP+GLP-1 agonist — the GIP component contributes to its superior weight loss vs GLP-1 monotherapy.

G05

GLP-1 (Glucagon-Like Peptide-1)

Incretin hormone that stimulates insulin release, suppresses glucagon, and delays gastric emptying. Semaglutide and Tirzepatide are GLP-1 agonists.

H

H01

Half-life

Time for plasma concentration to fall by 50%. Short-acting peptides (Ipamorelin: ~2h) require multiple daily injections. Long-acting (CJC-1295 with DAC: 7–10 days) require weekly injection.

H02

HGH

Human Growth Hormone. Identical to endogenously produced GH. Adult dosing per Endocrine Society: start 1 IU/day, titrate by IGF-I response. Weight-based dosing is NOT recommended for adults.

I

I01

IGF-1 (Insulin-Like Growth Factor 1)

Primary downstream mediator of GH action, produced mainly in the liver. Blood IGF-1 is the standard marker used to titrate GH/HGH doses.

I02

IGF-1 LR3

Long R3 IGF-1. Modified IGF-1 with reduced IGFBP binding — ~3× longer half-life (~20h vs ~6h). Reconstituted in 0.6% acetic acid.

I03

Ipamorelin

Selective GHRP. Stimulates GH release without raising cortisol or prolactin — considered the cleanest GHRP. Clinical trials: 1–3 mcg/kg SC.

I04

Insulin syringe units

Standard 1 ml insulin syringe = 100 units. Dose in units = volume (ml) × 100.

L

L01

Lyophilisate

The dry powder produced by lyophilization (freeze-drying). What arrives in the peptide vial before reconstitution.

M

M01

Melanotan II

Cyclic analogue of α-MSH. Activates MC1R (skin pigmentation) and MC4R (libido, erectile function). Weight-based dosing ~0.01 mg/kg. No regulatory approval.

N

N01

NAD+ (Nicotinamide Adenine Dinucleotide)

Coenzyme central to cellular energy metabolism and DNA repair. Levels decline ~50% between ages 40–60. Injectable protocols: 100–1,000 mg/session fixed.

P

P01

Peptide

Short chain of amino acids (2–50) linked by peptide bonds. Most research peptides are 5–30 amino acids. Larger chains are proteins (HGH = 191 amino acids).

P02

Proteolysis

Enzymatic degradation of peptides by proteases in the body. Most peptides have very short half-lives due to rapid proteolytic breakdown. Chemical modifications (amidation, PEGylation, DAC) extend stability.

R

R01

Reconstitution

Process of dissolving a lyophilized peptide powder in a liquid (usually bacteriostatic water) to create an injectable solution.

S

S01

SC (Subcutaneous injection)

Injection into the fat layer beneath the skin. Standard route for most research peptides. Common sites: abdomen, outer thigh, upper arm.

S02

Semaglutide

GLP-1 agonist. STEP trial: ~15% body weight loss over 68 weeks at 2.4 mg/week. Fixed escalation protocol regardless of body weight.

S03

Sermorelin

GHRH analogue. Adult dosing: 200–500 mcg fixed (NOT weight-based). Pediatric dosing (30 mcg/kg) is not applicable to adult research.

T

T01

TB-500

Synthetic fragment of Thymosin Beta-4 (Tβ4). Promotes actin polymerization, cell migration, and anti-inflammatory signalling. No human clinical trials — animal model only.

T02

Tesamorelin

GHRH analogue, FDA-approved for HIV-associated lipodystrophy at 2 mg/day fixed. Only GH peptide with confirmed human clinical indication.

T03

Thymosin Alpha-1

Immune-modulating peptide. 1.6 mg standard unit; FDA Orphan Drug designation. Fixed dose, not weight-dependent.

T04

Tirzepatide

Dual GIP+GLP-1 agonist. SURMOUNT-1 trial: ~20% body weight loss over 72 weeks. Fixed escalation 2.5→15 mg/week regardless of body weight.

V

V01

Vial (lyophilized)

Glass sealed container with lyophilized peptide powder. Common sizes: 1 mg, 2 mg, 5 mg, 10 mg. Typically stored at room temperature or refrigerated before reconstitution.

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