Neumeyer J L, Law S J, Meldrum B, Anlezark G, Watling K J
J Med Chem. 1981 Jul;24(7):898-9. doi: 10.1021/jm00139a027.
(-)-2,10,11-Trihydroxy-N-n-propylnoraporphine (TNPA,2c) has been synthesized from thebaine (3a), via northebaine (3b), normorphothebaine (2a), and alkylation to the N-propyl derivative 2b. O-Demethylation gave the desired product 2c. Compound 2c showed activity comparable to its 10,11-dihyroxy counterpart (NPA, 1b) on the stimulation of dopamine-sensitive adenylate cyclase in carp retinal homogenates. The evaluation of 2c on audiogenic seizures in mice, in the protection against paroxysimal EEG and myoclonic response to photic stimulation in the baboon, revealed a similar pharmacological profile in comparison to NPA and apomorphine, with TNPA showing a prolonged duration of action in abolishing myoclonic response to photic stimulation in the baboon.
(-)-2,10,11-三羟基-N-正丙基去甲阿朴啡(TNPA,2c)已从蒂巴因(3a)出发,经去甲蒂巴因(3b)、去甲吗啡蒂巴因(2a)合成,并烷基化得到N-丙基衍生物2b。O-去甲基化得到所需产物2c。在鲤鱼视网膜匀浆中,化合物2c在刺激多巴胺敏感腺苷酸环化酶方面表现出与其10,11-二羟基类似物(NPA,1b)相当的活性。对2c在小鼠听源性惊厥方面的评估,以及在狒狒中对阵发性脑电图和对光刺激的肌阵挛反应的保护作用评估,发现与NPA和阿扑吗啡相比,其药理特征相似,TNPA在消除狒狒对光刺激的肌阵挛反应方面显示出延长的作用持续时间。