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Methods for modulating nuclear receptor coactivator binding

机译:调节核受体共激活因子结合的方法

摘要

The present invention relates to methods and agonist/antagonist compounds for modulating nuclear receptor coactivator binding. The invention includes a method for identifying residues comprising a coactivator binding site for a nuclear receptor of interest. Also included is a method of identifying agonists and/or antagonists that bind to a coactivator binding site of a nuclear receptor of interest. Agonists and antagonists of coactivator binding to nuclear receptors also are provided. The invention is exemplified by identification and manipulation of the coactivator binding site of the thyroid receptor (TR), and compounds that bind to this sites. The methods can be applied to other nuclear receptors including RAR, RXR, PPAR, VDR, ER, GR, PR, MR, and AR.
机译:本发明涉及用于调节核受体共激活剂结合的方法和激动剂/拮抗剂化合物。本发明包括一种用于鉴定残基的方法,该残基包含针对感兴趣的核受体的共活化剂结合位点。还包括鉴定与目标核受体的共激活子结合位点结合的激动剂和/或拮抗剂的方法。还提供了与核受体结合的辅助活化剂的激动剂和拮抗剂。通过鉴定和操纵甲状腺受体(TR)的辅助活化剂结合位点以及与该位点结合的化合物来举例说明本发明。该方法可以应用于其他核受体,包括RAR,RXR,PPAR,VDR,ER,GR,PR,MR和AR。

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