352304-04-2Relevant articles and documents
Synthesis and structure-activity relationships of uracil derived human GnRH receptor antagonists: (R)-3-[2-(2-amino)phenethyl]-1-(2,6-difluorobenzyl)-6- methyluracils containing a substituted thiophene or thiazole at C-5
Rowbottom, Martin W.,Tucci, Fabio C.,Connors Jr., Patrick J.,Gross, Timothy D.,Zhu, Yun-Fei,Guo, Zhiqiang,Moorjani, Manisha,Acevedo, Oscar,Carter, Lee,Sullivan, Susan K.,Xie, Qiu,Fisher, Andrew,Struthers, R. Scott,Saunders, John,Chen, Chen
, p. 4967 - 4973 (2007/10/03)
The design and synthesis of a number of 5-thiazolyl and 5-thienyl substituted uracils is described and results from SAR studies are summarized. The best compound showed Ki = 2 nM. The synthesis of a series of (R)-3-[2-(2-amino)phenethyl]-1-(2,6