Design and discovery of 1,3-benzodiazepines as novel dopamine antagonists.

Bioorganic & Medicinal Chemistry Letters(2009)

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摘要
A series of novel 1,3-benzodiazapine based D1 antagonists was designed according to the understanding of pharmacophore models derived from SCH 23390 (1b), a potent and selective D1 antagonist. The new design features an achiral cyclic-amidine that maintains desired basicity. Solid phase synthesis was developed for SAR development of the novel dopamine antagonists.
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关键词
Dopamine,D1 receptor antagonist,Benzodiazepine
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