Research · Peptide Hubs
Peptide Reference Hubs
Each hub is a structured cluster: a pillar page covering pharmacology, mechanism, and regulatory status, plus deep-dive articles on half-life, bioavailability, animal studies, human trials, and safety.
Tirzepatide
Mounjaro · Zepbound
Dual GIP / GLP-1 Receptor Agonist
Tirzepatide is a once-weekly dual GIP and GLP-1 receptor agonist approved for T2DM (Mounjaro) and chronic weight management (Zepbound). This pillar covers mechanism, half-life, bioavailability, pivotal trials, safety, and regulatory status.
t½ ≈ 5 days (mean t½ 116.7 h)F ≈ 80 % subcutaneous4 articlesOpen hubSemaglutide
Ozempic · Wegovy · Rybelsus
GLP-1 Receptor Agonist
Semaglutide is a GLP-1 receptor agonist approved for type 2 diabetes (Ozempic, Rybelsus) and chronic weight management (Wegovy). The SELECT trial demonstrated cardiovascular risk reduction in people with obesity but without diabetes. This pillar covers mechanism, half-life, pharmacokinetics, pivotal trials, safety, and regulatory status.
t½ approximately 165 hours (about 1 week)F approximately 89% subcutaneous; approximately 1% oral (with SNAC absorption enhancer)4 articlesOpen hubBPC-157
Synthetic pentadecapeptide, research compound
BPC-157 is a pentadecapeptide researched primarily in rodent models for potential effects on tendon, gastric mucosa, and other tissues. No regulatory agency has approved it for any therapeutic use. This page summarises preclinical findings, proposed mechanisms, the known limits of the evidence, and the research-only regulatory status in all covered jurisdictions.
t½ Not established in humans; very short in rats by some IV estimates (minutes to ~30 min)F Not established in humans; oral bioavailability suggested to be low based on animal data4 articlesOpen hubCJC-1295 and Ipamorelin
GHRH Analog (CJC-1295) combined with GHS-R1a Agonist / Ghrelin Receptor Agonist (Ipamorelin)
CJC-1295 (a GHRH analog) and Ipamorelin (a selective GHS-R1a agonist) are research peptides often discussed as a combination. This pillar covers their individual pharmacology, the rationale for combining them, available Phase I/II data, pharmacokinetics, and safety signals. Neither compound is approved in any jurisdiction.
t½ CJC-1295 without DAC: approximately 30 minutes. CJC-1295 with DAC: approximately 6-8 days. Ipamorelin: approximately 2 hours.4 articlesOpen hubLiraglutide
Victoza · Saxenda
GLP-1 Receptor Agonist
Liraglutide is a once-daily GLP-1 receptor agonist marketed as Victoza (diabetes) and Saxenda (weight management). This pillar covers structure, mechanism, half-life, the LEADER cardiovascular outcomes trial, the SCALE weight-management program, safety, and regulatory status across five major jurisdictions.
t½ ≈ 13 hours (allows once-daily dosing)F ≈ 55 % subcutaneous1 articlesOpen hubTB-500 (Thymosin Beta-4 / active fragment)
Actin-Sequestering Peptide / Tissue Repair Research Compound
TB-500 is a research compound marketed as synthetic Thymosin β4 or its active fragment. Not approved by FDA, EMA, MHRA, TGA, or Health Canada. This pillar covers Tβ4 biology, the actin-sequestration mechanism, available early-phase clinical data, and the absence of pivotal trial evidence.
t½ Not established in humans from published clinical dataF No published human pharmacokinetic data for subcutaneous route1 articlesOpen hubPT-141 (Bremelanotide)
Vyleesi
Melanocortin Receptor Agonist
PT-141 (bremelanotide) is a melanocortin receptor agonist approved as Vyleesi for HSDD in premenopausal women. This pillar covers the MC receptor pharmacology, RECONNECT Phase 3 trial data, key adverse effects (nausea, transient BP elevation), and regulatory status across five jurisdictions.
t½ ≈ 2.7 hoursF Subcutaneous on-demand dosing; Tmax approximately 1 hour after administration1 articlesOpen hubGHK-Cu (Copper Tripeptide-1)
Copper-Binding Tripeptide / Cosmetic Ingredient
GHK-Cu (Gly-His-Lys copper complex) is a naturally occurring tripeptide studied for wound healing, skin regeneration, and anti-inflammatory effects, mainly in fibroblast culture and small clinical observations. Not FDA, EMA, MHRA, TGA, or Health Canada approved for therapeutic use. Widely present in cosmetic formulations.
t½ Not established from published human pharmacokinetic studiesF Topical application studied in cosmetic and small wound studies; systemic bioavailability from topical route not established in peer-reviewed data1 articlesOpen hub