Synthesis and biological evaluation of new naphtho- and quinolinocyclopentane derivatives as potent melatoninergic (MT 1 /MT 2 ) and serotoninergic (5-HT 2C ) dual ligands
作者:Romain Duroux、Marouan Rami、Elodie Landagaray、Mohamed Ettaoussi、Daniel-Henri Caignard、Philippe Delagrange、Patricia Melnyk、Saïd Yous
DOI:10.1016/j.ejmech.2017.10.025
日期:2017.12
as constrained agomelatine analogues. Herein, in order to explore alternative ethyl amide side chain rigidification, naphthocyclopentane and quinolinocyclopentane derivatives with various acetamide modulations were synthesized and evaluated at both melatonin (MT1, MT2) and serotonin (5-HT2C) receptors. These modifications has led to compounds with promising dual affinity and high MTs receptors agonist
我们最近报道了一系列萘呋喃类化合物,它们被约束为阿戈美拉汀类似物。在本文中,为了探索替代的乙基酰胺侧链刚性,合成了具有各种乙酰胺调节作用的萘环戊烷和喹啉基环戊烷衍生物,并在褪黑激素(MT 1,MT 2)和5-羟色胺(5-HT 2C)受体上进行了评估。这些修饰已导致具有希望的双重亲和力和高MTs受体激动剂活性的化合物。然后在选定的化合物上进行对映体分离,从而使我们能够将左旋gyerent对映体(-)- 17g和(-)- 17k鉴定为最高(MT 1,MT 2)/ 5-HT 2C 当今描述的双配体。