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HISTAMINE H3 RECEPTOR AGONISTS FOR THERAPEUTIC USE, PHARMACEUTICAL PREPARATIONS THAT WORK ON H3 RECEPTORS AGONISTIC AND THE METHOD OF THEIR REPRESENTATION

机译:用于治疗性用途的组胺H3受体激动剂,用于H3受体的药物制剂及其代表方法

摘要

PCT No. PCT/FR91/00384 Sec. 371 Date Feb. 6, 1992 Sec. 102(e) Date Feb. 6, 1992 PCT Filed May 10, 1991 PCT Pub. No. WO91/17146 PCT Pub. Date Nov. 14, 1991.Agonist compounds of the histamine H3 receptor for therapeutic use, pharmaceutical compositions acting as agonists of the said receptor and preparation process are disclosed. The compounds are derived from an amine R-NH2 having a high affinity for the histamine H3 receptor and to the primary amine function of which a group which gives rise to a bond that is capable of being slowly hydrolyzed in a neutral medium is attached. The pharmaceutical compositions contain these compounds and a pharmaceutically acceptable vehicle or excipient. These compounds are used for producing a medicinal product which inhibits the synthesis and the release of histamine, in particular, possessing sedative, sleep-regulating, anticonvulsant, antidepressant, anti-allergic, anti-inflammatory, antisecretory or anti-ulcerous effects.
机译:PCT号PCT / FR91 / 00384第二部分371日期1992年2月6日102(e)日期,1992年2月6日,PCT,1991年5月10日提交,PCT Pub。 WO91 / 17146 PCT公开号1991年11月14日,公开了用于治疗用途的组胺H 3受体的激动剂化合物,用作所述受体的激动剂的药物组合物和制备方法。该化合物衍生自对组胺H3受体具有高亲和力的胺R-NH2,并且该胺的伯胺官能团连接有产生能够在中性介质中缓慢水解的键的基团。药物组合物包含这些化合物和药学上可接受的载体或赋形剂。这些化合物用于生产抑制组胺的合成和释放的药物,特别是具有镇静,睡眠调节,抗惊厥,抗抑郁,抗过敏,抗炎,抗分泌或抗溃疡作用。

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