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EP2 Antagonists (2011-2021): A Decade's Journey from Discovery to Therapeutics.


ABSTRACT: In the wake of health disasters associated with the chronic use of cyclooxygenase-2 (COX-2) inhibitor drugs, it has been widely proposed that modulation of downstream prostanoid synthases or receptors might provide more specificity than simply shutting down the entire COX cascade for anti-inflammatory benefits. The pathogenic actions of COX-2 have long been thought attributable to the prostaglandin E2 (PGE2) signaling through its Gαs-coupled EP2 receptor subtype; however, the truly selective EP2 antagonists did not emerge until 2011. These small molecules provide game-changing tools to better understand the EP2 receptor in inflammation-associated conditions. Their applications in preclinical models also reshape our knowledge of PGE2/EP2 signaling as a node of inflammation in health and disease. As we celebrate the 10-year anniversary of this breakthrough, the exploration of their potential as drug candidates for next-generation anti-inflammatory therapies has just begun. The first decade of EP2 antagonists passes, while their future looks brighter than ever.

SUBMITTER: Sluter MN 

PROVIDER: S-EPMC8455147 | biostudies-literature | 2021 Aug

REPOSITORIES: biostudies-literature

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EP2 Antagonists (2011-2021): A Decade's Journey from Discovery to Therapeutics.

Sluter Madison N MN   Hou Ruida R   Li Lexiao L   Yasmen Nelufar N   Yu Ying Y   Liu Jiawang J   Jiang Jianxiong J  

Journal of medicinal chemistry 20210805 16


In the wake of health disasters associated with the chronic use of cyclooxygenase-2 (COX-2) inhibitor drugs, it has been widely proposed that modulation of downstream prostanoid synthases or receptors might provide more specificity than simply shutting down the entire COX cascade for anti-inflammatory benefits. The pathogenic actions of COX-2 have long been thought attributable to the prostaglandin E2 (PGE<sub>2</sub>) signaling through its Gα<sub>s</sub>-coupled EP2 receptor subtype; however, t  ...[more]

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