Gonadorelin (6-D-Phe)
GnRH with D-phenylalanine at position 6: a veterinary GnRH agonist authorised in the UK (Gonavet, Oestracton) for cattle, pigs and horses.
Gonadorelin (6-D-Phe), listed by the UK regulator as gonadorelin[6-D-Phe], is a GnRH agonist made by putting D-phenylalanine in place of glycine 6 of gonadorelin, which makes it stable against enzymatic breakdown. It is authorised in the UK as the veterinary medicines Gonavet and Oestracton for cattle, pigs and horses. A German herd study gave it to 1,634 dairy cows after insemination to try to raise conception rates.
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Recommended Dosing
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Mechanism of action
A GnRH agonist analogue, stable against enzymatic degradation (2018 study); used to time ovulation in livestock.
Primary uses
- Ovulation control in cattle, pigs and horses (UK authorisations)
- Studied after insemination to raise conception rates in dairy cows
Typical dosing
No human dose: it is approved only for animals, and the veterinary label's dose is for the animal species named on it, so none is given here.
Regulatory status
Approved only for animals. UK: Gonavet (gonadorelin [6-D-Phe]) and Oestracton (gonadorelin [6-D-Phe] acetate), for cattle, horses and pigs, are currently authorised (VMD). Not in the US Green Book's active-ingredient list or the EMA medicines list; Drugs@FDA holds no record.
Status as of this entry's last review, October 28, 2026. Approvals, compounding rules and sport rules change; the regulatory tracker is checked more often.
What we checked
Gonadorelin (6-D-Phe) is a veterinary GnRH agonist; this section records what can be checked.
Identity, computed
| Structure | gonadorelin with D-phenylalanine at position 6 (the name; 2018 study) |
| Products | Gonavet and Oestracton (VMD) |
PubChem returned no record under this name on the read date, so no formula is given.
Regulatory status, read October 28, 2026
Drugs@FDA: 0 records for “gonadorelin [6-D-Phe]”. EMA medicines list: 0 records for “gonadorelin [6-D-Phe]”. Run for semaglutide, the same queries return 6 and 5 records (and the registry search 80 trials), so a zero here is an absence, not a broken search. WADA 2026: section S2.2.1; WADA 2027: section S2.2.1.
What the studies show
Given at insemination or 12 days later to 1,634 cows in a large Saxon dairy herd to raise conception rates (Freick et al., 2014).
Zinc-triggered self-assembly of the peptide into nanostructures and fibrils (Yordanova et al., 2018).
A 1991 study of a dose reduction by complexing D-Phe6-GnRH with polyglycine (Naumann et al., 1991).
What we looked for and did not find
No human study.
| Source | Query | Results, October 28, 2026 | What it was |
|---|---|---|---|
| PubMed | "gonadorelin [6-D-Phe]"[tiab] OR "D-Phe6-GnRH"[tiab] OR Gonavet[tiab] | 26 | |
| ClinicalTrials.gov | Gonavet | 0 | |
| Drugs@FDA (openFDA) | gonadorelin [6-D-Phe] | 0 | |
| EMA medicines list | gonadorelin [6-D-Phe] | 0 |
References
- [other] UK Veterinary Medicines Directorate, Product Information Database, currently authorised products searched by active substance, read October 28, 2026: Gonavet Veyx 50 µg/ml solution for injection for cattle, pigs and horses, VM 27569/4005, active substance gonadorelin[6-D-Phe]; Oestracton 52.4 micrograms/ml, VM 08007/5047, active substance gonadorelin[6-D-Phe] acetate. https://www.vmd.defra.gov.uk/ProductInformationDatabase/
- [clinical-trial] Freick M, et al. "[Use of gonadorelin[6-D-Phe] at day 0 or 12 after insemination to increase the conception rate in a large dairy herd in Saxony/Germany]." Tierarztl Prax Ausg G Grosstiere Nutztiere, 2014;42(6):331-42. PMID: 25401927.
- [pubmed] Yordanova Y, et al. "Zn(2+)-triggered self-assembly of Gonadorelin [6-D-Phe] to produce nanostructures and fibrils." Sci Rep, 2018;8(1):11280. PMID: 30050082.
- [pubmed] Naumann W, et al. "[Dosage reduction of d-phe-6-GnRH for the regulation of ovulation by complexation with polyglycine]." Pharmazie, 1991;46(11):795-7. PMID: 1811231.
- [other] US FDA, Drugs@FDA (openFDA): no application for gonadorelin [6-D-Phe]. Read October 28, 2026.
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Guides & tools
This entry is for educational purposes only and does not constitute medical advice. Dosing information reflects published regulatory or research data and is not a recommendation. Many compounds described here are not approved for human use in the United States. Consult a licensed medical professional before considering any peptide therapy.