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

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

机译:氟尿素和氟尿素衍生物抑制胰岛淀粉样蛋白形成的毒性作用

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 I) wherein R1 and R2 are each independently hydrogen, methyl, ethyl, propyl, butyl, pentyl or 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, propyl, butyl, pentyl or 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I)其中R 1和R 2各自独立氢,甲基,乙基,丙基,丁基,戊基或己基相连,或R1和R2连接形成环丙基,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,丙基,丁基,戊基或己基,或其药学上可接受的盐或酯,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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