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Discovery and Optimization of 7-Alkylidenyltetrahydroindazole-Based Acylsulfonamide EP3 Antagonists.

ABSTRACT: A novel series of 7-alkylidenyltetrahydroindazole-based acylsulfonamides were discovered as potent EP3 antagonists. The initial lead compound 7 exhibited potent in vitro EP3 inhibitory activity and good selectivity against other EP receptors. In addition, compound 7 demonstrated in vivo activity in a rat ivGTT model, reversing the suppressive effect of the EP3-specific agonist sulprostone on glucose-stimulated insulin secretion. Further optimization to improve the pharmacokinetic profile led to the discovery of compounds 26 and 28 with potent in vitro activity and significantly lower in vivo clearance and higher oral exposure than compound 7.

SUBMITTER: Zhu B

PROVIDER: S-EPMC8762748 | biostudies-literature | 2022 Jan

REPOSITORIES: biostudies-literature

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Discovery and Optimization of 7-Alkylidenyltetrahydroindazole-Based Acylsulfonamide EP3 Antagonists.

Zhu Bin B Zhang Xuqing X Guo Lili L Rankin Matthew M Bakaj Ivona I Ho George G Lee Seunghun P SP Norquay Lisa L Macielag Mark M

ACS medicinal chemistry letters 20211207 1

A novel series of 7-alkylidenyltetrahydroindazole-based acylsulfonamides were discovered as potent EP3 antagonists. The initial lead compound <b>7</b> exhibited potent in vitro EP3 inhibitory activity and good selectivity against other EP receptors. In addition, compound <b>7</b> demonstrated in vivo activity in a rat ivGTT model, reversing the suppressive effect of the EP3-specific agonist sulprostone on glucose-stimulated insulin secretion. Further optimization to improve the pharmacokinetic p ...[more]

PMID: 35059130

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