3,4-Disubstituted indole acylsulfonamides: A novel series of potent and selective human EP3 receptor antagonists-Reference-Cited by-同舟云学术

3,4-Disubstituted indole acylsulfonamides: A novel series of potent and selective human EP3 receptor antagonists

Published:2009-01 Issue:1 Volume:19 Page:123-126
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Zhou Nian,Zeller Wayne,Krohn Michael,Anderson Herb,Zhang Jun,Onua Emmanuel,Kiselyov Alex S.,Ramirez Jose,Halldorsdottir Guðrún,Andrésson Þorkell,Gurney Mark E.,Singh Jasbir

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference19 articles.

1. The utilization of recombinant prostanoid receptors to determine the affinities and selectivities of prostaglandins and related analogs

2. Ligand binding specificities of the eight types and subtypes of the mouse prostanoid receptors expressed in Chinese hamster ovary cells

3. Prostaglandin E2 both stimulates and inhibits adenyl cyclase on platelets: Comparison of effects on cloned EP4 and EP3 prostaglandin receptor subtypes

4. Interaction of prostaglandin E2 and β-adrenergic catecholamines in the regulation of uterine smooth muscle motility and adenylate cyclase in the rat

5. Prostanoid inhibition of canine parietal cells: Mediation by the inhibitory guanosine triphosphate-binding protein of adenylate cyclase

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