Degarelix
GnRH antagonist for advanced prostate cancer management. Immediate testosterone suppression without initial flare effect, providing rapid and sustained castration-level hormone reduction.
Degarelix is a synthetic decapeptide (10 amino acids) and a third-generation gonadotropin-releasing hormone (GnRH) receptor antagonist. It is approved for the treatment of advanced hormone-dependent prostate cancer. Unlike GnRH agonists, degarelix directly blocks GnRH receptors in the pituitary gland without causing an initial testosterone surge (clinical flare), providing immediate and sustained testosterone suppression to castration levels. Its unique molecular structure incorporates non-natural amino acids including D-2-naphthylalanine, D-4-chlorophenylalanine, and D-3-pyridylalanine, which confer high binding affinity (IC50 = 3 nM) and selectivity for the GnRH receptor with minimal histamine release.
| Parameter | Specification |
| CAS | 214766-78-6 |
| Molecular Formula | C₈₂H₁₀₃ClN₁₈O₁₆ |
| Molecular Weight | 1632.26 g/mol |
| Category | GnRH/Reproductive |
| Purity | ≥99% |
| Status | GMP-compliant, FDA-ready |
| Applications | Advanced prostate cancer, testosterone suppression, fertility research |
| CAS | 214766-78-6 |
|---|---|
| Applications | Advanced Prostate Cancer, Hormone-dependent Tumors, Testosterone Suppression |




