Incretin & metabolic signalling
The metabolic category is where incretin research sits: GLP-1, GIP and glucagon receptor agonists, plus the GHRH and monoamine compounds studied around body-composition endpoints. It is the deepest category in the catalogue, and the one where mechanism differences matter most when choosing a compound. Priced and shipped in CAD, for laboratory and research use only.
The incretin compounds separate cleanly by how many receptors they engage. Semaglutide is a GLP-1 receptor agonist. Tirzepatide is a dual GLP-1/GIP agonist. Retatrutide is a triple GLP-1/GIP/glucagon agonist and the newest of the three. GLP-1 receptor agonists compared covers the class; for head-to-head detail see retatrutide vs tirzepatide and tirzepatide vs semaglutide.
Tesamorelin is a GHRH analogue studied specifically around visceral adipose tissue — a different axis entirely from the incretins. Tesofensine is a triple monoamine reuptake inhibitor, a small molecule rather than a peptide. AOD-9604 is a growth-hormone fragment studied around lipolysis without the full GH signalling profile.
This category is the main reason the reloadable 3 mL pen format exists — retatrutide is stocked as a pen alongside 10 mg, 15 mg, 20 mg and 30 mg vials. Pens change the reconstitution arithmetic because the volume is fixed; the dosage calculator handles both formats.
Because these compounds share mechanisms with named pharmaceuticals, the comparison content is where most questions land: retatrutide vs Ozempic, semaglutide vs tirzepatide, tirzepatide vs Mounjaro and generic semaglutide in Canada. The fat-loss foundations protocol covers research design. All of it is research framing — none of these compounds is supplied for human use.
Tesofensine side effects — what the research reports
Tesofensine side effects by evidence tier: the dose-dependent heart-rate and blood-pressure rise, dry mouth, insomnia and mood signals from the Phase 2 and 3 trials, and the gaps.
Tesofensine dosage — research dosing notes
What the tesofensine trials administered: the 0.25–1.0 mg once-daily oral doses of TIPO-1 and the Mexican Phase 3, the nine-day half-life and weeks-long accumulation, and titration.
AOD-9604 side effects — what the research reports
AOD-9604 side effects by evidence tier: the pooled six-trial tolerability data from the oral Phase 1 and 2 programme, the GRAS and FDA positions, animal work, and the injectable-route gap.
AOD-9604 dosage — research dosing notes
What the literature reports on AOD-9604 dosage: the 1–30 mg oral trial doses, rodent mg/kg protocols, the absent injectable half-life, and reconstitution math for a 2.5 mg vial.
Tesamorelin side effects — what the research reports
Tesamorelin side effects from the Egrifta Phase 3 trials and monograph: injection-site reactions, arthralgia, oedema, glucose and IGF-1 signals, and why none of it transfers to research-grade vials.
AOD-9604 — a research overview
A research overview of the AOD-9604 peptide: the hGH 177-191 fragment, its proposed β3-adrenergic lipolysis mechanism, what the Phase 2a and Phase 2b human trials actually returned, and its regulatory status.
Research & educational use only. This page is informational and does not constitute medical advice or a therapeutic claim.

Canada Peptides
RETATRUTIDE 15 MG
GLP-1 / GIP / GCG
$120.00·Metabolic