Pascal J C, Beranger S, Pinhas H, Poizot A, Désiles J P
J Med Chem. 1985 May;28(5):647-52. doi: 10.1021/jm50001a019.
A series of 3,4-dihydro-1,3-dimethyl-7-[3-(4-substituted-piperazin-1-yl)- substituted-alkyl]-1H-purine-2,6-diones and 3,7-dihydro-3,7-dimethyl-1-[3-(4-substituted-piperazin-1-yl)- substituted-alkyl]-1H-purine-2,6-diones was synthesized and evaluated for antihistaminic activity. Some of them displayed good inhibition of both histamine-induced bronchospasm in the anesthetized guinea pig at 10 micrograms/kg by the intravenous route and of passive cutaneous anaphylaxis in the rat at 10 mg/kg by the oral route. Comparison of the two most active compounds revealed a higher antihistaminic activity with the compounds containing a (phenylthio)propyl group (1 and 2) as compared with that containing a phenoxy group. Compound 2 [RS-49014, 3,4-dihydro-1,3-dimethyl-7-[3-[4-[3-(phenylthio)propyl]piperazin-1 -yl]- 2-hydroxypropyl]-1H-purine-2,6-dione] was selected for clinical trials on the basis of a comparative pharmacological study with chlorpheniramine, ketotifen, promethazine, and theophylline.
合成了一系列3,4 - 二氢 - 1,3 - 二甲基 - 7 - [3 - (4 - 取代 - 哌嗪 - 1 - 基) - 取代 - 烷基] - 1H - 嘌呤 - 2,6 - 二酮和3,7 - 二氢 - 3,7 - 二甲基 - 1 - [3 - (4 - 取代 - 哌嗪 - 1 - 基) - 取代 - 烷基] - 1H - 嘌呤 - 2,6 - 二酮,并对其抗组胺活性进行了评估。其中一些化合物在静脉注射10微克/千克时,对麻醉豚鼠组胺诱导的支气管痉挛,以及在口服10毫克/千克时,对大鼠被动皮肤过敏反应均表现出良好的抑制作用。比较两种活性最高的化合物发现,与含有苯氧基的化合物相比,含有(苯硫基)丙基的化合物(1和2)具有更高的抗组胺活性。基于与氯苯那敏、酮替芬、异丙嗪和茶碱的比较药理学研究,选择化合物2 [RS - 49014,3,4 - 二氢 - 1,3 - 二甲基 - 7 - [3 - [4 - [3 - (苯硫基)丙基]哌嗪 - 1 - 基] - 2 - 羟丙基] - 1H - 嘌呤 - 2,6 - 二酮]进行临床试验。