Endocrine & immune signalling
Foundational covers compounds studied at the upstream signalling level — the HPG axis, melanocortin receptors, and immune modulation — rather than a downstream performance endpoint. These sit apart from the other categories because their research context is the regulatory system itself. Priced and shipped in CAD, for laboratory and research use only.
Kisspeptin sits at the top of the hypothalamic-pituitary-gonadal cascade, studied as an upstream regulator of GnRH release. That places it above the compounds it is usually grouped with — hCG, for instance, acts as an LH analogue further down the same axis.
PT-141 (bremelanotide) is a melanocortin receptor agonist with MC4R selectivity, studied around central rather than peripheral signalling. It shares a receptor family with Melanotan 2 but differs in selectivity, which is why the two are catalogued separately rather than as variants of one compound.
Thymosin alpha-1 is a thymic peptide studied around T-cell maturation and immune signalling. It is mechanistically unrelated to TB-500 despite the shared thymosin name — TB-500 is a thymosin-β4 fragment studied around actin remodelling and sits under recovery. The naming overlap is a common source of confusion.
Thymosin alpha-1 side effects — what the research reports
Thymosin alpha-1 side effects by evidence tier: tolerability recorded in the thymalfasin trials and Zadaxin post-marketing record, the mechanistic cautions and the gaps for research-grade material.
Thymosin alpha-1 dosage — research dosing notes
What the thymalfasin trials and the Zadaxin label report about thymosin alpha-1 dosage: the 1.6 mg subcutaneous unit dose, its cadences, the 2-hour half-life and 5 mg vial arithmetic.
Kisspeptin side effects — what the research reports
Kisspeptin side effects by evidence tier: what several hundred volunteers in the human physiology and IVF studies showed, the predictable endocrine effects, tachyphylaxis, and the gaps.
Kisspeptin dosage — research dosing notes
What the human kisspeptin studies reported: kisspeptin-10 versus kisspeptin-54, intravenous and subcutaneous doses, the IVF-trigger trials, tachyphylaxis, and reconstitution math for a 10 mg vial.
PT-141 side effects — what the research reports
PT-141 side effects from the phase 3 bremelanotide trials and FDA label: nausea, flushing, transient blood pressure changes, focal hyperpigmentation, and where the data runs out.
PT-141 dosage — research dosing notes
What the literature reports on PT-141 dosage: the 1.75 mg subcutaneous regimen from the RECONNECT Phase 3 trials, the ~2.7-hour half-life, the eight-dose monthly ceiling, and reconstitution math for a 10 mg vial.
Research & educational use only. This page is informational and does not constitute medical advice or a therapeutic claim.