化学
受体
敌手
前列腺素D2
药理学
效力
体外
生物化学
生物
作者
Christian Beaulieu,Daniel Guay,Zhaoyin Wang,Yves Leblanc,Patrick Roy,Claude Dufresne,Robert Zamboni,Carl Berthelette,Stephen H. Day,Nancy N. Tsou,Danielle Denis,Gillian Greig,Marie‐Claude Mathieu,Gary P. O’Neill
标识
DOI:10.1016/j.bmcl.2008.03.015
摘要
A new series of indole-based antagonists of the PGD(2) receptor subtype 1 (DP1 receptor) was identified and the progress of the structure-activity relationship study to the identification of potent and selective antagonists is presented. Selective DP1 antagonists with high potency and selectivity were prepared. Of particular interest is the DP1 antagonist 26 with a K(i) value of 1 nM for the DP1 receptor and an IC(50) value of 4.6 nM in a DP1 functional assay for the inhibition of the PGD(2) induced cAMP production in platelet rich plasma (PRP).
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