GH Secretagogues

Sermorelin

Also known as: GRF 1-29

Molecular Identifiers

Molecular Formula

C149H246N44O42S

CAS Number

86168-78-7

PubChem CID

16132413

Molecular Weight

3357.96 Da

Overview

GHRH analog with gentle GH stimulation. Suitable for long-term protocols. Good option for anti-aging research with a conservative profile.

The main clinical interest around sermorelin is stimulating endogenous growth hormone (GH) secretion from the pituitary in a physiological way — preserving natural negative feedback via somatostatin, unlike exogenous recombinant GH replacement. The sought effects are support for REM sleep, recovery, body composition, and quality of life in adults with age-related decline of somatotropic function.

It was originally FDA-approved as Geref (1990) for the diagnosis and treatment of GH deficiency in children, but its commercial production was discontinued in the U.S. in 2008. Today it circulates mostly as off-label use through compounding pharmacies in anti-aging and functional endocrinology medicine, in evening 12+ week subcutaneous protocols, often combined with GHRP peptides (ipamorelin, GHRP-2) for synergistic stimulation. WADA lists GHRH and its analogs as substances prohibited in sports competition.

It corresponds to fragment 1-29 of native human GHRH — the minimal portion that retains full biological activity on the GHRH receptor in the anterior pituitary.

Among GHRH analogs, sermorelin is the most "natural" — native human sequence, with no modifications to extend half-life — and therefore the shortest-acting: it contrasts with Mod GRF 1-29 (CJC-1295 without DAC, more stable), with CJC-1295 with DAC (weekly dosing via albumin binding), and with tesamorelin (FDA-approved modified analog for HIV lipodystrophy). It acts on the GHRH receptor and is therefore often combined with a GHRP (ipamorelin, GHRP-2, GHRP-6, or hexarelin) or contrasted with MK-677, which mimics ghrelin via the oral route.

Sequence (1 letter): YADAIFTNSYRKVLGQLSARKLLQDIMSR
Extended notation: Tyr-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

Half-life

~10-20 minutes

Administration Route

Subcutaneous

Category

GH Secretagogues

Mechanism of Action

  • Native GHRH analog (fragment 1-29)
  • Physiological stimulation of GH secretion
  • Preserves natural negative feedback
  • Promotes REM sleep and recovery

Dosage Protocol

Data compiled from the literature. This does not constitute medical advice.

Parameter Value
Dose 200-500 mcg per injection
Frequency Once daily
Timing Before bedtime
Duration 12+ weeks

Reported Side Effects

Adverse effects described in the literature. Severity and frequency vary between individuals.

  • Facial flushing
  • Headache
  • Dizziness
  • Injection site pain
  • Drowsiness

Product Properties

Purity >99%
Appearance White lyophilized powder
Solubility Soluble in water and bacteriostatic water
Source Solid-phase peptide synthesis (SPPS)
Storage Lyophilized: -20°C for up to 2 years, 2-8°C for up to 6 months. Reconstituted: 2-8°C for up to 4 weeks. Protect from light and moisture. Avoid repeated freeze-thaw cycles.

Presentations & Preparation

Vials of Sermorelin found in the research market:

2 mg5 mg15 mg

Reconstitution

  • Diluent: Bacteriostatic water
  • Volume: 2 ml per 5 mg vial
  • Slowly inject the diluent against the vial wall
  • Gently swirl until fully dissolved
  • Never shake

Storage

  • Lyophilized: Refrigerated 2-8°C
  • Reconstituted: Refrigerated 2-8°C (up to 30 days)
  • Protect from direct light
  • Do not freeze after reconstitution
Reconstitution Calculator

Scientific Studies

Published studies on Sermorelin.

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