作者: Hongliang Duan , Jin Zheng , Qinglin Lai , Zheng Liu , Guanghui Tian
DOI: 10.1016/J.BMCL.2009.03.125
关键词:
摘要: In our efforts to minimize the side effects associated with low selectivity against other PDE isozymes, a novel class of 2-phenylquinazolin-4(3H)-one derivatives were designed and prepared as potent PDE5 inhibitors high PDE6. The syntheses SAR studies such molecules reported.