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Sermorelin

GH-axis research

Sermorelin

Péptido de investigación de señalización endocrina liofilizado para revisión de sistemas

Sermorelin is a GHRH 1-29 analog studied as a classic pituitary GH-axis research reference.

Rango de precios: desde 45.99 $ hasta 195.99 $
98.7%-99.3% Polvo liofilizado 5 mg
Available documentation

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For laboratory research use only. Not for human or veterinary use. Not intended to diagnose, treat, cure, mitigate, or prevent disease.

Storage

Mantener sellado, frío, seco y protegido de los cambios de calor. Confirme el almacenamiento específico del producto a su llegada.

Notas de envío

Empaquetado para estabilidad en tránsito con soporte de pedidos disponible para rutas en climas cálidos.

Batch reference

Batch-linked certificate support is available through the documentation desk.

Contexto de investigación

Perfil de investigación de Sermorelin

Sermorelin is a 29-amino-acid analog corresponding to the active amino-terminal region of growth hormone-releasing hormone. It is used as a classic reference for pituitary GHRH-receptor signaling, stimulated GH release, endocrine responsiveness, and downstream IGF-1 measurements. Compared with CJC-1295 with DAC, sermorelin represents a shorter GHRH framework without the same half-life-extension design. Compared with ipamorelin and GHRP peptides, it acts through a different receptor pathway. Researchers generally select sermorelin when the study calls for a well-established GHRH 1-29 reference or a direct comparison of pituitary signaling across GHRH analogs and ghrelin-receptor secretagogues.

Molecular class

44-residue GHRH 1-44 analog

Sequence / composition

A synthetic amino-terminal 44-residue segment corresponding to the receptor-active region of human GHRH.

Research design note

It is a direct GHRH-receptor reference, unlike GH secretagogues that act through GHS-R.

Mecanismo propuesto

A synthetic GHRH(1-29) peptide that activates the pituitary GHRH receptor, increases cyclic AMP, and stimulates endogenous growth-hormone release from responsive somatotroph cells.

Efectos reportados en estudios

  • Human diagnostic and pharmacology studies reported acute GH release and used the response to evaluate pituitary reserve.
  • Downstream changes can include transient increases in GH and IGF-1-related markers when repeated exposure is studied.
  • Responses vary with age, pituitary function, endogenous somatostatin tone, timing, and prior exposure.

Criterios de investigación comunes

GHRH receptor signaling, cyclic AMP, peak and integrated GH, IGF-1, pituitary responsiveness, age-related response, pharmacokinetics, and comparison with longer-acting GHRH analogs.

Evidencia y limitaciones

The GHRH stimulation mechanism is well characterized, including historical human diagnostic use. This does not establish therapeutic equivalence of a catalog product.

External reading

Literature for context—not product proof.

Third-party sources describe their own research materials and methods. They do not validate a specific Azure catalog batch.

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