Structure–activity relationship studies on ortho-substituted cinnamic acids, a new class of selective EP3 antagonists-Reference-Cited by-同舟云学术

Structure–activity relationship studies on ortho-substituted cinnamic acids, a new class of selective EP3 antagonists

Published:2005-02 Issue:3 Volume:15 Page:527-530
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Belley Michel,Gallant Michel,Roy Bruno,Houde Karine,Lachance Nicolas,Labelle Marc,Trimble Laird A.,Chauret Nathalie,Li Chun,Sawyer Nicole,Tremblay Nathalie,Lamontagne Sonia,Carrière Marie-Claude,Denis Danielle,Greig Gillian M.,Slipetz Deborah,Metters Kathleen M.,Gordon Robert,Chan Chi Chung,Zamboni Robert J.

Publisher

Elsevier BV

Subject

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

Reference20 articles.

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

2. Prostanoid Receptors: Structures, Properties, and Functions

3. Distribution and function of prostanoid receptors: studies from knockout mice

4. Synthesis and structure–activity relationships of a new class of selective EP 3 receptor agonist, 13,14-didehydro-16-phenoxy analogues of prostaglandin E 1

5. Function of prostanoid receptors: studies on knockout mice

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