Molecules (Dec 2017)

Recent Development of Non-Peptide GnRH Antagonists

  • Feng-Ling Tukun,
  • Dag Erlend Olberg,
  • Patrick J. Riss,
  • Ira Haraldsen,
  • Anita Kaass,
  • Jo Klaveness

DOI
https://doi.org/10.3390/molecules22122188
Journal volume & issue
Vol. 22, no. 12
p. 2188

Abstract

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The decapeptide gonadotropin-releasing hormone, also referred to as luteinizing hormone-releasing hormone with the sequence (pGlu-His-Trp-Ser-Tyr-Gly-Leu-Arg-Pro-Gly-NH2) plays an important role in regulating the reproductive system. It stimulates differential release of the gonadotropins FSH and LH from pituitary tissue. To date, treatment of hormone-dependent diseases targeting the GnRH receptor, including peptide GnRH agonist and antagonists are now available on the market. The inherited issues associate with peptide agonists and antagonists have however, led to significant interest in developing orally active, small molecule, non-peptide antagonists. In this review, we will summarize all developed small molecule GnRH antagonists along with the most recent clinical data and therapeutic applications.

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