Gallagher G, Lavanchy P G, Webster C A, Wilson J W, Hieble J P, DeMarinis R M
J Med Chem. 1985 Oct;28(10):1533-6. doi: 10.1021/jm00148a028.
4-[2-(Di-n-propylamino)ethyl]-2(3H)-indolone (1c) (SK&F 101468) is a potent and selective prejunctional dopamine receptor agonist. It caused a dose-related inhibition of the constrictor response to electrical stimulation in the isolated perfused rabbit ear artery (EC50 = 100 nM), and this response was antagonized by (S)-sulpiride (KB = 7 nM). Compound 1c did not stimulate or block dopamine-sensitive adenylate cyclase and did not produce stimulation of the central nervous system in rats. It was prepared from (2-methyl-3-nitrophenyl)acetic acid in a multistep sequence based on the Reissert indole synthesis.
4-[2-(二正丙基氨基)乙基]-2(3H)-吲哚酮(1c)(SK&F 101468)是一种强效且选择性的突触前多巴胺受体激动剂。它对离体灌流兔耳动脉中电刺激引起的收缩反应产生剂量相关的抑制作用(半数有效浓度=100 nM),并且该反应可被(S)-舒必利拮抗(平衡解离常数=7 nM)。化合物1c不刺激或阻断多巴胺敏感的腺苷酸环化酶,也不会在大鼠中产生中枢神经系统刺激作用。它是由(2-甲基-3-硝基苯基)乙酸根据赖歇特吲哚合成法经多步反应制备而成。