化学
选择性
同工酶
立体化学
化学合成
酶抑制剂
组合化学
结构-活动关系
酶
生物化学
体外
催化作用
作者
Hongliang Duan,Jin Zheng,Qinglin Lai,Zheng Liu,Guanghui Tian,Zhen Wang,Jianfeng Li,Jingshan Shen
标识
DOI:10.1016/j.bmcl.2009.03.125
摘要
In our efforts to minimize the side effects associated with low selectivity against the other PDE isozymes, a novel class of 2-phenylquinazolin-4(3H)-one derivatives were designed and prepared as potent PDE5 inhibitors with high selectivity against PDE6. The syntheses and SAR studies of such molecules were reported.
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