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Issue 10, 2017
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Small molecule piperazinyl-benzimidazole antagonists of the gonadotropin-releasing hormone (GnRH) receptor

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Abstract

In this communication, we report the synthesis and characterization of a library of small molecule antagonists of the human gonadotropin releasing hormone receptor based upon the 2-(4-tert-butylphenyl)-4-piperazinyl-benzimidazole scaffold via Cu-catalysed azide alkyne cycloaddition. Our main purpose was to find a more soluble compound based on the WAY207024 lead with nanomolar potency to inhibit the GnRH receptor. A late stage diversification by the use of click chemistry was, furthermore developed to allow for expansion of the library in future optimisations. All compounds were tested in a functional assay to determine the individual potency of inhibiting stimulation of the receptor by the endogenous agonist GnRH. In conclusion, we found that compound 8a showed improved solubility compared to WAY207024 and nanomolar affinity to GnRH receptor.

Graphical abstract: Small molecule piperazinyl-benzimidazole antagonists of the gonadotropin-releasing hormone (GnRH) receptor

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Publication details

The article was received on 26 Jun 2017, accepted on 13 Sep 2017 and first published on 14 Sep 2017


Article type: Research Article
DOI: 10.1039/C7MD00320J
Citation: Med. Chem. Commun., 2017,8, 1965-1969
  • Open access: Creative Commons BY license
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    Small molecule piperazinyl-benzimidazole antagonists of the gonadotropin-releasing hormone (GnRH) receptor

    R. Fjellaksel, M. Boomgaren, R. Sundset, I. H. Haraldsen, J. H. Hansen and P. J. Riss, Med. Chem. Commun., 2017, 8, 1965
    DOI: 10.1039/C7MD00320J

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