For laboratory research use only. Not for human or animal consumption.
BioIntegrityPeptide Research

Growth Factors

Sermorelin

GHRH analog

Sermorelin (GHRH(1-29)-NH₂)

Research context

Sermorelin corresponds to the first 29 residues of endogenous GHRH with a C-terminal amide, the shortest sequence reported to retain full receptor activity. Research examines GHRH receptor binding, cAMP accumulation, and growth hormone release in pituitary cell preparations, often as the unmodified reference against stabilised analogues.

Common assays: GHRH receptor binding · cAMP accumulation · Pituitary GH secretion

Specification

DesignationGHRH analog
Full nameSermorelin (GHRH(1-29)-NH₂)
SequenceTyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-NH₂
CAS number86168-78-7
Molecular formulaC149H246N44O42S
Molecular weight3357.88 g/mol
Formats10 mL Vial
SolubilityBacteriostatic water, sterile water
StorageLyophilised: 2–8 °C, protected from light. Reconstituted: 2–8 °C.

Published literature

Selected peer-reviewed references describing research involving this compound. Listed for reference only; inclusion is not a claim about any outcome.

  1. Walker RF.Sermorelin: a better approach to management of adult-onset growth hormone insufficiency?Clinical Interventions in Aging · 2006 Find on PubMed ↗

Common questions

How does sermorelin relate to CJC-1295 and tesamorelin?

All three target the GHRH receptor. Sermorelin is the unmodified 1-29 fragment; CJC-1295 is the same fragment with four internal substitutions for enzymatic stability; tesamorelin is the full 44-residue sequence with an N-terminal acyl group.

Why is the 1-29 fragment used rather than full-length GHRH?

Published structure-activity work found the N-terminal 29 residues sufficient for receptor activity, giving a shorter sequence that is simpler to synthesise and characterise.

Components, blends and pathway

Related compounds