Research Overview
CJC-1295 with DAC
The peptide is a 29-residue GHRH fragment with four amino-acid substitutions (D-Ala2, Gln8, Ala15, Leu27) chosen to resist dipeptidyl peptidase-4 cleavage and chemical degradation, plus a lysine-linked maleimidopropionyl group at the C-terminus. That maleimide reacts with the free thiol of albumin cysteine-34 shortly after entering circulation, tethering the analogue to a long-lived carrier protein. Published pharmacokinetic work reports a residence time measured in days rather than minutes, which is the defining difference from unmodified GRF analogues.
Ipamorelin
Why the combination is studied
- The two peptides engage separate receptors with separate second-messenger routes, allowing additive-versus-synergistic questions to be tested.
- Ipamorelin also acts on somatostatin tone, a mechanism distinct from direct GHRH-receptor stimulation.
- Pairing a long-acting analogue with a short-acting one lets investigators separate sustained baseline signalling from discrete pulses.