Title of article
2,3-Diarylthiophenes as selective EP1 receptor antagonists
Author/Authors
Yves Ducharme، نويسنده , , Marc Blouin، نويسنده , , Marie-Claude Carrière، نويسنده , , Anne Chateauneuf، نويسنده , , Bernard Côté، نويسنده , , Danielle Denis، نويسنده , , Richard Frenette، نويسنده , , Gillian Greig، نويسنده , , Stacia Kargman، نويسنده , , Sonia Lamontagne، نويسنده , , Evelyn Martins، نويسنده , , François Nantel، نويسنده , , Gary O’Neill، نويسنده , , Nicole Sawyer، نويسنده , , Kathleen M. Metters، نويسنده , , Richard W. Friesen، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2005
Pages
6
From page
1155
To page
1160
Abstract
The synthesis and the EP1 receptor binding affinity of 2,3-diarylthiophene derivatives are described. The evaluation of the structure–activity relationship (SAR) in this series led to the identification of compounds 4, 7, and 12a, which exhibit high affinity for the human EP1 receptor and a selectivity greater than 100-fold against the EP2, EP3, EP4, DP, FP, and IP receptors and greater than 25-fold versus the TP receptor. These three antagonists present good pharmacokinetics in rats and significant differences in the way they are distributed in the brain.
Keywords
Prostaglandin E2 , EP1 Receptor antagonist
Journal title
Bioorganic & Medicinal Chemistry Letters
Serial Year
2005
Journal title
Bioorganic & Medicinal Chemistry Letters
Record number
795355
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