首页> 外国专利> THE INHIBITION OF THE TOXIC EFFECTS OF ISLET AMYLOID FORMATION BY FLURBIPROFEN AND FLURBIPROFEN DERIVATIVES

THE INHIBITION OF THE TOXIC EFFECTS OF ISLET AMYLOID FORMATION BY FLURBIPROFEN AND FLURBIPROFEN DERIVATIVES

机译:氟比洛芬和氟比洛芬衍生物对胰岛淀粉样蛋白形成的毒性作用的抑制作用

摘要

The subject invention provides a method of reducing the presence of toxic intermediates of amyloidosis from islet amyloid polypeptide (IAPP) in a patient, comprising administering a compound to the patient a compound having the structure: (Formula 1) wherein R1 and R2 are each independently hydrogen, methyl, ethyl, propyl, butyl, pentyl, hexyl, or R1 and R2 are linked so as to form a cyclopropyl cyclobutyl, cyclopentyl, or cyclohexyl ring; wherein R3, R4, R5, R6 are each independently hydrogen, fluorine or chlorine; and wherein R7 is hydrogen, phenyl, fluorine, chlorine, bromine, hydroxyl, amine, carboxylic acid, C1-C6 alkyl carboxylate, amide, methyl, ethyl, butyl, pentyl, hexyl, or a pharmaceutically acceptable salt or ester thereof, so as to thereby reduce the presence of toxic intermediates of amyloidosis from islet amyloid polypeptide (IAPP) in the patient.
机译:本发明提供了一种减少患者体内来自胰岛淀粉样多肽(IAPP)的淀粉样变性病的毒性中间体的存在的方法,该方法包括向患者施用具有以下结构的化合物:(式1)其中R 1和R 2各自独立氢,甲基,乙基,丙基,丁基,戊基,己基或R 1和R 2连接以形成环丙基环丁基,环戊基或环己基环;其中R3,R4,R5,R6各自独立地为氢,氟或氯;其中R7是氢,苯基,氟,氯,溴,羟基,胺,羧酸,C1-C6烷基羧酸酯,酰胺,甲基,乙基,丁基,戊基,己基或其药学上可接受的盐或酯,因此从而减少患者体内来自胰岛淀粉样多肽(IAPP)的淀粉样变性病的毒性中间体的存在。

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