Discovery and optimization of novel, non-steroidal glucocorticoid receptor modulators
摘要:
A virtual screening approach comprising a 3-D similarity search based on known GR modulators was used to identify a novel series of non-steroidal glucocorticoid receptor (GR) antagonists. Optimization of the initial hit to provide potent compounds which exhibit good selectivity against other steroidal nuclear hormone receptors is described. (C) 2007 Elsevier Ltd. All rights reserved.
The present invention provides a novel class of modified pyrimidine compounds and compositions and methods of using the compounds as glucocorticoid receptor modulators.
本发明提供了一类新型的改良嘧啶化合物,以及使用这些化合物作为糖皮质激素受体调节剂的组合物和方法。
Preparation of 5-substituted benzylbarburituric acids and investigation of the effect of the benzyl and substituted benzyl groups on the acidity of barbituric acid
作者:John V. Tate、William N. Tinnerman、Vito Jurevics、Harold Jeskey、Edward R. Biehl
DOI:10.1002/jhet.5570230103
日期:1986.1
5-substituted benzylbarbituric acids has been determined in 50% ethanol/water and they were found to be more acidic than barbituric acid. The pKas of these derivatives obey Hammett's equation indicating that their acidity is affected by substituents in the same manner as the benzoic acid ionization constants. A synthesis of these acids is described.
已在50%的乙醇/水中测定了5-苄基巴比妥酸和一系列5-取代的苄基巴比妥酸的酸度,发现它们比巴比妥酸更酸性。这些衍生物的p K a s服从哈米特方程,表明它们的酸度受取代基影响的方式与苯甲酸电离常数相同。描述了这些酸的合成。
The present invention provides a novel class of modified pyrimidine compounds and compositions and methods of using the compounds as glucocorticoid receptor modulators.