4.7 Article

Advances in the Development of Nonpeptide Small Molecules Targeting Ghrelin Receptor

Journal

JOURNAL OF MEDICINAL CHEMISTRY
Volume 65, Issue 4, Pages 3098-3118

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jmedchem.1c02191

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Funding

  1. University of Camerino (Fondo di Ateneo per la Ricerca 2019)

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This article discusses the role of ghrelin and its receptor GHS-R1a in multiple physiological processes and their potential in treating various disorders. It also introduces the development of nonpeptide small molecules as GHS-R1a agonists, antagonists, and inverse agonists in recent years, as well as the pharmacological effects of the most studied ligands.
Ghrelin is an octanoylated peptide acting by the activation of the growth hormone secretagogue receptor, namely, GHS-R1a. The involvement of ghrelin in several physiological processes, including stimulation of food intake, gastric emptying, body energy balance, glucose homeostasis, reduction of insulin secretion, and lipogenesis validates the considerable interest in GHS-R1a as a promising target for the treatment of numerous disorders. Over the years, several GHS-R1a ligands have been identified and some of them have been extensively studied in clinical trials. The recently resolved structures of GHS-R1a bound to ghrelin or potent ligands have provided useful information for the design of new GHS-R1a drugs. This perspective is focused on the development of recent nonpeptide small molecules acting as GHS-R1a agonists, antagonists, and inverse agonists, bearing classical or new molecular scaffolds, as well as on radiolabeled GHS-R1a ligands developed for imaging. Moreover, the pharmacological effects of the most studied ligands have been discussed.

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