
Sermorelin GHRH(1-29) Research Peptide
GHRH(1-29) Amide · Minimal GHRH Fragment · GH Secretagogue
Sermorelin (GRF 1-29) is the minimal GHRH fragment - 29 amino acids that retain full GH-releasing activity and serve as the DPP-stability reference for every longer GHRH analog.
Size: 5mg
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Lab Tested
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COA
Publicly Available
CAS Number
86168-78-7
Molecular Weight
3357.93 g/mol
There is a specific research question that only the shortest viable GHRH fragment can answer: how much does N-terminal protection actually extend half-life? To quantify the improvement with longer analogs like tesamorelin, you need the unprotected baseline. That's sermorelin.
Sermorelin (GRF(1-29), CAS 86168-78-7) is the synthetic 29-amino-acid C-terminal amide analog corresponding to GHRH residues 1-29 - the minimal fragment that retains full GH-releasing activity at GHRH-R on pituitary somatotrophs. MW 3357.93 g/mol, formula C149H246N44O42S. It signals through Gs/adenylyl-cyclase/cAMP, stimulating pulsatile GH release just as native GHRH does - but without the N-terminal protection of tesamorelin, it is subject to dipeptidyl-peptidase cleavage at the N-terminus, making it the standard DPP stability reference for the GHRH class.
We supply Sermorelin at ≥99% HPLC purity in 5mg and 10mg vials. For in vitro laboratory research use only.
Key Takeaways
Key Scientific Specifications
Research-Referenced Attributes
Based on published preclinical and clinical literature; not therapeutic claims. For laboratory research use only.
Related Compounds

GLP-3 RT
Single and dual GLP-1 agonists leave GCGR activation on the table. GLP-3 RT (Retatrutide) hits all three - GLP-1R, GIPR, and GCGR - the only way to model true triple-receptor crosstalk.

GLP-3 R
GLP-3R is the lipidated variant - a 39-amino-acid GLP-1R/GIPR/GCGR triagonist with a fatty acid conjugate that extends half-life and alters receptor-binding kinetics vs. unlipidated analogs.