化学
化学合成
药物发现
组合化学
立体化学
体外
生物化学
作者
Laurent Provins,Bernard Christophe,Pierre Danhaive,Jacques Dulieu,Véronique Durieu,Michel Gillard,Florence Lebon,Sébastien Lengelé,Luc Quéré,BerendJan van Keulen
标识
DOI:10.1016/j.bmcl.2006.01.006
摘要
SAR around 4,6-diaminopyrimidine derivatives allowed the discovery of the first potent dual M3 antagonists and PDE4 inhibitors. Various chemical modulations around that scaffold led to the discovery of ucb-101333-3 which is characterized by the most interesting profile on both targets.
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