首页> 外国专利> ANALOG OF L-ARGININE EXHIBITING INHIBITION ACTIVITY TO NO SYNTHASE, PROCESS OF ITS PREPARATION AND PHARMACEUTICAL COMPOSITION CONTAINING THEREOF

ANALOG OF L-ARGININE EXHIBITING INHIBITION ACTIVITY TO NO SYNTHASE, PROCESS OF ITS PREPARATION AND PHARMACEUTICAL COMPOSITION CONTAINING THEREOF

机译:L-精氨酸对无合酶的抑制活性类似物,其制备过程及包含其的药物成分

摘要

In the present invention there are disclosed L-arginine derivatives of the general formula I, in which A represents hydrogen, alkyl containing 1 to 6 carbon atoms or NOi2, E represents oxygen or a covalent bond, n is zero or an integer ranging from 1 through 12 and Ri1 and Ri2 represent independently on each other a branched or straight alkyl group containing 1 to 6 carbon atoms or Ri1 and Ri2 form together with a nitrogen atom to which they are attached a ring of the formula b wherein Xi1 represents an alkylene or alkenylene chain having 1 to 2 carbon atoms, Xi2 represents methylene or ?CH= and X represents an oxygen, sulfur or nitrogen atom, an imino group, an alkylimino group having 1 to 6 carbon atoms or an ethylene radical, and their pharmaceutically acceptable salts. These derivatives are useful for preparing medicaments intended for treating pathologies of central and peripheral nervous system, pathological dysfunction of digestive and urinary tract of inflammatory or non-inflammatory type and pathologies connected with cardiovascular or bronchopulmonary systems. There are also described processes for preparing the derivatives, medicaments, as well as use of these derivatives for preparing medicaments based on these substances.
机译:在本发明中公开了通式I的L-精氨酸衍生物,其中A代表氢,含1至6个碳原子的烷基或NO 12,E代表氧或共价键,n为零或1的整数。式12至12和Ri1和Ri2彼此独立地表示含有1至6个碳原子的支链或直链烷基,或者Ri1和Ri2与它们所连接的氮原子一起形成式b的环,其中Xi1代表亚烷基或具有1-2个碳原子的亚烯基链,Xi2表示亚甲基或αCH=,X表示氧,硫或氮原子,亚氨基,具有1-6个碳原子的烷基亚氨基或亚乙基,及其药学上可接受的盐。这些衍生物可用于制备用于治疗中枢和周围神经系统病理,炎性或非炎性类型的消化道和泌尿道的病理功能障碍以及与心血管或支气管肺系统有关的病理的药物。还描述了制备衍生物,药物的方法,以及这些衍生物在基于这些物质制备药物中的用途。

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