📜5-甲氧基-2-萘满酮置于platinum(Iv) Oxide 氢气,对甲苯磺酸体系中,用 乙醇,苯 用作溶剂,化学反应 19.5H,反应生成5-甲氧基-1,2,3,4-四氢-N-(苯甲基)-2-萘胺
参考文献:2-Amido-8-Methoxytetralins: A Series Of Nonindolic Melatonin-Like Agents
标题:2-Amido-8-Methoxytetralins: A Series Of Nonindolic Melatonin-Like Agents
摘要:A Series Of Unsubstituted And Methoxy-Substituted 2-Amidotetralins (4A-Q) Was Prepared And Evaluated For Their Ability To Compete For 2-[i-125]Iodomelatonin Binding To Chicken Retinal Membranes And For Their Potency To Inhibit The Calcium-Dependent Release Of [h-3]Dopamine From Rabbit Retina. The Lead Compound,2-Acetamido-8-Methoxytetralin (4J),Showed A Moderate Affinity (K(I) = 46 Nm) And Potency (Ic50 = 1.4 Nm) At The Melatonin Receptor. The Structural Requirements Necessary For Optimal Agonistic Activity At The Melatonin Receptor Are As Follows. First,The Amido Group,Which Should Have A Small,Nonbranched Alkyl Group,Is Essential For Affinity,And Second,The Methoxy Substituent At The 8-Position Of The 2-Amidotetralin Ring Is Essential For Optimal Agonistic Activity At The Melatonin Receptor. We Concluded That This Series Of Unsubstituted And Methoxy-Substituted 2-Amidotetralins Constitutes A Class Of Nonindolic Melatonin-Like Agents That Can Be Used As Pharmacological Tools To Further Characterize Melatonin Receptors And To Elucidate The Mode Of Action Of Melatonin.
Doi:10.1021/jm00072A008