作者: Mickaël Jean , Jacques Renault , Nicolas Levoin , Denis Danvy , Thierry Calmels
DOI: 10.1016/J.BMCL.2010.07.096
关键词:
摘要: Isosteric replacement of the amide function and modulation arylpiperazine moiety known dopamine D3 receptor ligands led to potent selective compounds. Enhanced bioavailability preferential brain distribution make compound 6c a good candidate for pharmacological clinical evaluation.