352290-71-2Relevant articles and documents
3-(2-Aminoalkyl)-1-(2,6-difluorobenzyl)-5-(2-fluoro-3-methoxyphenyl) -6-methyluracils as orally bioavailable antagonists of the human gonadotropin releasing hormone receptor
Tucci, Fabio C.,Zhu, Yun-Fei,Guo, Zhiqiang,Gross, Timothy D.,Connors Jr., Patrick J.,Gao, Yinghong,Rowbottom, Martin W.,Struthers, R. Scott,Reinhart, Greg J.,Xie, Qiu,Chen, Ta Kung,Bozigian, Haig,Bonneville, Anne L. Killam,Fisher, Andrew,Jin, Liping,Saunders, John,Chen, Chen
, p. 3483 - 3486 (2007/10/03)
Uracils possessing N-3 side chains derived from various amino alcohols were designed and synthesized as potent human gonadotropin releasing hormone receptor antagonists. The compounds herein presented displayed superior metabolic stability than their pred