摘要
选择超短时作用型镇静催眠药zolpidem作为先导化合物 ,设计合成了 8个 2 芳基 α 烷氧基咪唑〔1,2 α〕并吡啶 3 乙酰胺类目标物 ,所有化合物均未见文献报道 .药理初筛结果表明 :目标化合物对小鼠有镇静作用 。
On the basis of structural analysis,zolpidem,a hypnotic and sedative,was selected as a lead compound.Eight derivatives of 2 aralkyl α alkyloxide imidazo〔1,2 α〕pyridine 3 acetylamine were designed and synthesized.All of them had never been reported in literature.Preliminary pharmacological tests showed that the target compounds possessed certain hypnotic activity on mice.
出处
《中国药物化学杂志》
CAS
CSCD
2000年第2期95-99,共5页
Chinese Journal of Medicinal Chemistry