What is Half-Life? (Peptide Glossary)
Half-Life: The time for half of a compound to be cleared or degraded - the key pharmacokinetic property that determines research dosing frequency.
Half-life is the time required for half of a substance to be eliminated or degraded. It is the single most important pharmacokinetic property for research design because it dictates dosing frequency: a peptide with a 30-minute half-life (like Mod GRF 1-29) produces short pulsatile exposure, while a week-long half-life (like semaglutide) supports once-weekly administration.
Research peptide engineering is largely the art of extending half-life. Native peptides are often degraded within minutes by enzymes. Common stabilization strategies visible across compound profiles include fatty acid chains that bind albumin (semaglutide's C18 chain extends it to ~7 days), DAC (Drug Affinity Complex) conjugation in CJC-1295, D-amino acid substitutions that resist proteases, and cyclization (Melanotan II).
When comparing related compounds, half-life differences define their research use. CJC-1295 with DAC (6-8 day half-life) produces sustained GH elevation in research models, while the no-DAC version (30 minutes) produces physiological pulses - the same base molecule with opposite pharmacokinetic characters. Compound pages on this site list published half-life data for exactly this reason.
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