Half-life
Pharmacokinetic decay constant
Half-life (t½) is the time required for the plasma concentration of a compound to fall to half its previous value. For peptide research, half-life governs three practical decisions: dosing frequency, time to steady state, and the overlap window when stacking compounds.
After approximately five half-lives, a compound is considered effectively eliminated (≈97%). Conversely, a compound dosed at fixed intervals reaches steady state after about 4–5 half-lives. That is why semaglutide (t½ ~7 days) takes roughly 5 weeks to reach steady state, while BPC-157 (t½ ~4 hours) is at steady state within a single day.
Plasma half-life is not always the same as effect half-life. DSIP and Semax both have very short systemic half-lives but produce CNS effects that outlast their measurable plasma concentration; TB-500’s effects on tissue regeneration similarly outlast plasma levels.
Used in 5 research peptides
- PerformanceIGF-1 DESTruncated IGF-1 with localized hypertrophic action; favored for site-specific bodybuilding research.
- PerformanceMGF (Mechano Growth Factor)IGF-1Ec splice variant released by mechanical loading; activates muscle satellite cells.
- MetabolicDulaglutideWeekly GLP-1 receptor agonist fused to an IgG4 Fc fragment; sold as Trulicity by Eli Lilly.
- MetabolicLixisenatideShort-acting prandial GLP-1 agonist; sold as Adlyxin/Lyxumia by Sanofi.
- CognitiveN-Acetyl SemaxAcetylated, more stable analog of Semax; longer-acting nootropic via BDNF/NGF upregulation.
See also
Educational use only
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