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GnRH agonist (nonapeptide analog)

Deslorelin

Deslorelin is a synthetic GnRH agonist peptide used primarily in veterinary medicine.

By The Peptides Codex Editorial TeamIndividual review date not recorded

Page data last changed: . Chemistry registry snapshot: . Registry refreshes and identity assessments are separate from scientific content review.

Length
9 aa
Class
GnRH agonist (nonapeptide analog)
Function
Gonadotropin-releasing hormone superagonist
Context
Approved for veterinary use (e.g., chemical castration in dogs, ovulation timing in mares); marketed as Suprelorin and Ovuplant

A GnRH superagonist used chiefly in veterinary medicine as a slow-release implant.

Also known as: Suprelorin · Ovuplant · GnRH agonist

Part of the Foundational & therapeutic peptides cluster

Overview

Deslorelin is a synthetic GnRH agonist peptide used primarily in veterinary medicine. As implants such as Suprelorin and Ovuplant, it is applied for reversible chemical castration in dogs and for ovulation timing in mares. This page is educational and is not medical advice.

Source & context

Biological / chemical source: Synthetic GnRH analog

Primary research or clinical context: Approved for veterinary use (e.g., chemical castration in dogs, ovulation timing in mares); marketed as Suprelorin and Ovuplant

Veterinary context

Deslorelin implants provide sustained GnRH receptor activation that, after an initial stimulatory phase, suppresses reproductive hormones. Veterinary applications include managing fertility and behavior in dogs, ferrets, and other species, and controlling reproduction in livestock and companion animals.

Superagonist chemistry

Like other clinical GnRH analogs, deslorelin carries a D-amino-acid substitution at position 6 and a modified C-terminus. These changes raise receptor potency and slow degradation, which is why it is described as a GnRH superagonist.

Sequence

One-letter sequence commonly cited for Deslorelin (educational; isoforms and modifications may differ):

XHWSYWLRP

XHWSYWLRP

X = non-canonical residue (Glutamic acid (residue 1) is pyroglutamic acid; leucine residue at position 6 is D-Trp; C-terminal proline residue at Pro-NHEt). X marks a non-canonical residue — see the structure block below. (Plotted as alanine on the wheel.)

Deslorelin9 aa · C64H83N17O12 · ≈ 1,282.4 DaPEPTIDESCODEX.COMN-terminus →→ C-terminusX1H2W3S4Y5W6L7R+8P9nonpolarpolaracidicbasicGly / Pronon-canonical (X)Hydropathy (Kyte–Doolittle): ▮ hydrophobic (cyan) / ▮ hydrophilic (rose) · Side-chain charge at pH 7: + / −X = non-canonical residue (Glutamic acid (residue 1) is pyroglutamic acid; leucine residue at position 6 is …
Deslorelin — Structure cardDownload SVG
A1H2W3S4Y5W6L7R8P9
Helical wheel projection

Residues plotted ~100° apart around an α-helix — clustering of one color reveals an amphipathic face.

Analyze sequences in the playground →

Structure & chemistry

Molecular identity & reference confidence

Source-supported reference

Reference values are taken from the cited molecular record or curated profile. A database match is not independent laboratory verification; modifications, counter-ions, and formulations can change the measured mass.

Molecular form
Deslorelin (source record; form not independently established)
Species
Not established by this molecular identity audit
Termini (N / C)
Not specified / Not specified

Average reference mass

Reference policy updated: 2026-10-05

Molecular formula
C64H83N17O12
Average reference mass
≈ 1,282.4
Chemical modifications (IUPHAR record)

Glutamic acid (residue 1) is pyroglutamic acid; leucine residue at position 6 is D-Trp; C-terminal proline residue at Pro-NHEt

Identifiers

Chemistry values: IUPHAR/BPS Guide to Pharmacology, PubChem · fetched 2026-10-01.

Clinical development snapshot

ClinicalTrials.gov lists 4 registered studies with “Deslorelin” as an intervention (snapshot 2026-10-01). A registry footprint is not evidence of efficacy or approval.

Registered studies
4
Highest phase reached
Phase 3
Active in latest 100
0
Most recent update
2025-06-12
Most recently updated studies
NCTTitlePhaseStatusUpdated
NCT00001521Three Drug Combination Therapy Versus Conventional Treatment of Children With Congenital Adrenal HyperplasiaPhase 3completed2025-06-12
NCT00080756Deslorelin Combined With Low-Dose Add-Back Estradiol and Testosterone in Preventing Breast Cancer in PremenopaPhase 2unknown2024-08-28
NCT00001190Study of Luteinizing Hormone-Releasing Hormone Analog (LHRHa) in Pubertal Patients With Extreme Short StaturePhase 2completed2008-03-04
NCT00001202Treatment of Boys With Precocious PubertyPhase 2completed2008-03-04
See all on ClinicalTrials.gov →
Concentration math

Deslorelin — reconstitution calculator

Enter how much peptide is in the vial and how much diluent (e.g. bacteriostatic water) is added. The tool returns the resulting solution concentration — and, for any amount you type, the volume it corresponds to. This is educational arithmetic, not a dosing recommendation.

Reference form: Deslorelin (source record; form not independently established)Average reference mass: 1,282.4 Da

Syringe graduation
Solution concentration
5 mg/mL5,000 mcg/mL
mcg

Enter an amount to see the volume it corresponds to.

Educational concentration mathematics only. This tool does not recommend a dose, amount, or protocol, and nothing here is medical advice. Many peptides are not authorized by Health Canada for human use — see our reconstitution and bacteriostatic-water guides for context.

Open the Deslorelin calculator on its own page →

FAQ about Deslorelin

What is Deslorelin?+

Deslorelin is a synthetic GnRH agonist peptide used primarily in veterinary medicine. As implants such as Suprelorin and Ovuplant, it is applied for reversible chemical castration in dogs and for ovulation timing in mares. This page is educational and is not medical advice.

What Canadian product status is recorded for Deslorelin?+

Canadian product status for Deslorelin has not been verified in this profile. No verified record here does not mean no authorization exists. Status depends on the product, formulation and use; consult Health Canada's product records.

What is the typical length of Deslorelin?+

Deslorelin is commonly described as approximately 9 amino acids (GnRH agonist (nonapeptide analog)).

Related peptides

References & further reading

  1. 1.Cowl et al. (2018). ASSESSING THE EFFICACY OF DESLORELIN ACETATE IMPLANTS (SUPRELORIN) IN ALTERNATIVE PLACEMENT SITES. J Zoo Wildl Med
  2. 2.Fontaine (2015). Long-term contraception in a small implant: A review of Suprelorin (deslorelin) studies in cats. J Feline Med Surg
  3. 3.Wolf et al. (2012). Litter size response to oestrous induction with deslorelin (Ovuplant®) in dogs. Reprod Domest Anim
  4. 4.Agnew et al. (2021). DESLORELIN (SUPRELORIN(®)) USE IN NORTH AMERICAN AND EUROPEAN ZOOS AND AQUARIUMS: TAXONOMIC SCOPE, DOSING, AND EFFICACY. J Zoo Wildl Med
  5. 5.Hemberg et al. (2006). Successful timing of ovulation using deslorelin (Ovuplant) is labour-saving in mares aimed for single ai with frozen semen. Reprod Domest Anim
  6. 6.Padula et al. (2003). Absorbable deslorelin implants (Ovuplant) prolong postpartum anestrus in early ovulating dairy cows. Theriogenology
  7. 7.McCue et al. (2002). Removal of deslorelin (Ovuplant) implant 48 h after administration results in normal interovulatory intervals in mares. Theriogenology
  8. 8.Palm et al. (2012). [The use of deslorelin acetate (Suprelorin®) in companion animal medicine]. Schweiz Arch Tierheilkd
  9. 9.PubChem — compound summary for Deslorelin (CID 16133804)
  10. 10.Wikipedia — Deslorelin
Disclaimer: Educational content only. Not medical advice. Not instructions for human use. Research peptides and unapproved products may be restricted or illegal to market for human consumption in your jurisdiction. Consult qualified professionals and applicable law.
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