首页> 外国专利> process of obtaining synthetic and semi-synthetic derivatives of lignans, their antiparasitic activities and their pharmaceutical formulations, encompassing the therapeutic method using such lignans in the treatment of parasitic diseases.

process of obtaining synthetic and semi-synthetic derivatives of lignans, their antiparasitic activities and their pharmaceutical formulations, encompassing the therapeutic method using such lignans in the treatment of parasitic diseases.

机译:获得木脂素的合成和半合成衍生物的方法,其抗寄生虫活性及其药物制剂,包括使用这种木脂素治疗寄生虫病的治疗方法。

摘要

"PROCESS FOR OBTAINING SYNTHETIC AND SEMISINTETIC DERIVATIVES OF LIGNAN, ITS ANTIPARASITARY ACTIVITIES AND THEIR PHARMACEUTICAL FORMULATIONS, ENGAGING THERAPEUTIC METHOD USING SUCH PARTAALS". The present invention relates to a process for obtaining synthetic and semi-synthetic lignan derivatives, in particular dibenzylbutyrolactonic, tetrahydrofuran, aryltetraline, furofuran and dibenzocyclooctanic lignans obtained by partial synthesis and / or total isolation. from plant extracts. Refers to a process for obtaining synthetic and semi-synthetic cubebin derivatives such as: (-) - O-acetyl cubebin; (-) - Omethyl cubebin; (-) - O-N, N- (dimethylamino-ethyl) -cuboline; (-) - hyinoquinine; (-) - 6.6? Dinitroinoquinine; (-) - O-benzyl cubebin; (-) - 6-6 39 -diaminoinoquinine, (-) - 6-6 39 dinitroinoquinine, as well as obtaining dibenzocyclooctanic lignans from dibenzylbutyrolactonic lignans by structural changes at positions 7, 7 39, 8 , 8 39, 9 39 and aromatic rings (introduction and / or substitution of functional groups such as: -OH, CO ~ 2 ~ H, -CO ~ 2 ~ CH ~ 3 ~, -NO ~ 2 ~, -NH ~ 2 ~, -OCH ~ 3 ~, -OAc, -SO ~ 2 ~ CH ~ 3 ~, -SO ~ 2 ~ NH ~ 2 ~, prenyl and halogens). The invention also relates to a therapeutic method since the described substances are used in the manufacture of medicaments which provide antiparasitic activity.
机译:“获得Lignan的合成和亚半精基衍生物,其抗寄生虫活性及其药物配方的过程,采用这种分部进行治疗性方法”。本发明涉及获得合成的和半合成的木脂聚糖衍生物的方法,特别是通过部分合成和/或完全分离得到的二苄基丁内酯,四氢呋喃,芳基四氢呋喃,呋喃呋喃和二苯并环辛基木脂聚糖。从植物提取物中提取。指获得合成的和半合成的立方蛋白衍生物的方法,例如:(-)-O-乙酰基立方蛋白; (-)-Omethyl cubebin; (-)-O-N,N-(二甲基氨基-乙基)-cubline; (-)-氨基奎宁; (-)-6.6?二硝基奎宁; (-)-O-苄基立方体; (-)-6-6 39-二氨基基奎宁,(-)-6-6 39二硝基基奎宁,以及通过位置7、7 <39>,8、8 <上的结构变化从二苄基丁内酯木脂素中获得二苯并环辛基木脂素。 39>,9 <39>和芳香环(引入和/或取代官能团,例如:-OH,CO〜2〜H,-CO〜2〜CH〜3〜,-NO〜2〜,-NH〜 2〜,-OCH〜3〜,-OAc,-SO〜2〜CH〜3〜,-SO〜2〜NH〜2〜,异戊二烯和卤素)。本发明还涉及一种治疗方法,因为所描述的物质被用于制造提供抗寄生虫活性的药物。

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