| Pcs | Single Vial, 3-Pack, 6-Pack, Pack of 10 |
|---|---|
| Strength | 5mg |
Gonadorelin Acetate
Price range: $35.00 through $308.00
UPS Ground $9.95. Free at $150. Orders before 2 pm ET ship the same business day.
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VERIFICATION
How to read this report
Gonadorelin Acetate, in structural terms.
- Sequence
- pGlu-His-Trp-Ser-Tyr-Gly-Leu-Arg-Pro-Gly-NH₂ One-letter-style representation: pE-H-W-S-Y-G-L-R-P-G-NH₂ This is the native mammalian GnRH decapeptide sequence; FDA documentation notes that gonadorelin has the same amino-acid sequence as the natural hormone.
- Molecular formula
- C₅₅H₇₅N₁₇O₁₃
- Molecular weight
- Approximately 1182.3 g/mol
- CAS number
- 33515-09-2 — Gonadorelin The FDA substance database identifies this as the primary CAS for gonadorelin.
- Peptide length
- 10 amino acids
- Structure type
- Linear peptide
- Primary molecular target
- Gonadotropin-Releasing Hormone Receptor (GnRHR / GnRH1R) GnRHR is the principal receptor through which GnRH regulates anterior pituitary gonadotroph signaling and gonadotropin secretion.
- Physical form
- Lyophilized powder
- PubChem CID
- 638793
Gonadorelin is a synthetic decapeptide structurally identical to endogenous gonadotropin-releasing hormone (GnRH). It consists of ten amino-acid residues with an N-terminal pyroglutamyl residue and an amidated C-terminus. This compact peptide structure functions as the endogenous ligand framework for the GnRH receptor and serves as a reference molecule for studying GnRH receptor signaling and modified GnRH analogs.Formula and molecular weight are for gonadorelin base. The marketed material is named Gonadorelin Acetate; the certificate does not state acetate stoichiometry, so no fixed acetate formula is published here.
Where Gonadorelin Acetate appears in the literature.
- GnRH receptor signaling studies
- GnRH receptor-binding research
- Pituitary gonadotroph studies
- LH secretion research
- FSH secretion research
- Hypothalamic-pituitary-gonadal axis research
- Pulsatile GnRH signaling models
- GnRH receptor desensitization studies
- Relevant published experimental systems include:
- GnRH receptor-expressing cell systems
- Isolated pituitary-cell models
- Anterior pituitary gonadotroph models
- Receptor-transfected cell systems
- GnRH receptor-binding models
- Gonadotropin secretion systems
- Reproductive endocrine models
- HPLC-UV purity analysis
- LC-MS identity confirmation
- Mass-confirmation analysis
- LAL endotoxin assay
- GnRH receptor-binding assays
- Competitive ligand-binding assays
- LH secretion assays
- FSH secretion assays
- Chromatographic purity
- Peptide identity
- Net peptide content
- Endotoxin assay result
- GnRH receptor binding
- LH release
- FSH release
- Gonadotroph signaling
What has been studied, and in what systems.
Gonadorelin is the synthetic form of endogenous GnRH and functions as an agonist of the gonadotropin-releasing hormone receptor.
GnRH receptor activation on anterior pituitary gonadotroph cells initiates intracellular signaling associated with synthesis and secretion of the gonadotropins luteinizing hormone (LH) and follicle-stimulating hormone (FSH).
The biological response to GnRH is strongly influenced by the temporal pattern of receptor stimulation, making Gonadorelin particularly relevant to experimental research involving pulsatile endocrine signaling, receptor desensitization, and hypothalamic-pituitary communication.
Because Gonadorelin reproduces the endogenous GnRH peptide sequence, it should be distinguished from structurally modified, longer-acting GnRH agonists whose substitutions can substantially alter receptor affinity, degradation resistance, and pharmacology. Research comparing GnRH and modified analogs demonstrates that peptide substitutions can materially alter receptor-binding affinity.
These are published research systems. They do not describe approved clinical applications, and they do not establish efficacy or safety in humans.
Flanagan CA et al., 1998. A high affinity gonadotropin-releasing hormone (GnRH) tracer, radioiodinated at position 6, facilitates analysis of mutant GnRH receptors. Endocrinology. PMID 9751490. https://pubmed.ncbi.nlm.nih.gov/9751490/
Loumaye E et al., 1982. Binding affinity and biological activity of gonadotropin releasing hormone agonists in isolated pituitary cells. Endocrinology. PMID 6286282. https://pubmed.ncbi.nlm.nih.gov/6286282/
About this compound and its batch data.
What is gonadorelin acetate?
Gonadorelin is a decapeptide, ten amino acids in length, structurally identical to endogenous gonadotropin-releasing hormone. Astramide supplies the acetate salt form as a lyophilized powder for laboratory research use only. It is not intended for human or animal consumption, clinical use, or therapeutic application.
Is gonadorelin the same as GnRH?
Gonadorelin is the synthetic form of gonadotropin-releasing hormone, also written GnRH or LHRH in the literature. The three names refer to the same decapeptide sequence. The acetate designation refers to the salt form the peptide is supplied in, not to a different molecule.
What purity does the current gonadorelin lot reach?
Lot GND5 returned 99.94% chromatographic purity, tested by Freedom Diagnostics under accession 2606080472. Identity was confirmed by LC-MS match to the labelled compound. The full Certificate of Analysis is published on the lot record and is downloadable as the laboratory’s own PDF.
How much gonadorelin is in the vial?
The label claim is 5 mg. Lot GND5 measured 5.84 mg, above label claim. Astramide publishes the measured figure for every lot, whether it sits above or below the claim, and the release criterion is at or above label claim.
How is Astramide's gonadorelin tested?
Lot GND5 was analysed by five methods at Freedom Diagnostics: identity by LC-MS, chromatographic purity, net content, endotoxin, and visual appearance. Endotoxin passed 2 of 2 replicates at or below 0.05 EU/mL. Appearance was reported as white lyophilized powder. Heavy metals, microbial and pH were not performed on this lot, and the report says so.
How should gonadorelin acetate be stored for research use?
Lyophilized material is stored at -20C and protected from light. Once reconstituted, storage is 2 to 8C with use within 14 to 30 days. Results from this lot apply to material handled within these conditions.
What is the difference between research-grade and pharmaceutical-grade gonadorelin?
These are separate classifications. Research-grade material is supplied for laboratory research use only and is not manufactured, tested or released under the regulatory framework that governs drugs for human use. Pharmaceutical-grade is an FDA classification for human-use products. Astramide supplies research-grade material exclusively.
This product is intended strictly for in-vitro laboratory research conducted by qualified professionals. It is not intended for human or animal consumption, clinical use, or therapeutic application. The statements on this page have not been reviewed by the FDA. These research peptides are not intended to diagnose, treat, cure, or prevent any disease. Research Use Only.






