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METHOD FOR THE TREATMENT OF THE COMPLICATIONS AND PATHOLOGY OF DIABETES

机译:糖尿病并发症和病理学的治疗方法

摘要

The present invention provides a method for the treatment of the complicationsand pathology of diabetes. The methodinvolves the administration to a diabetic subject of a composition comprisinga compound selected from the group consisting of(.beta.-Ala-His)n, (Lys-His)n, a compound of the formula R1-X-R2,pharmaceutically acceptable salts thereof and combinationsthereof; and a pharmaceutically acceptable carrier, in which n is 2-5, R1 isone or two naturally occurring amino acids,optionally alpha-amino acetylated with alkyl or aralkyl of 1 to 12 carbonatoms, preferably 2 to 6 carbon atoms, R2 is 1 or 2naturally occurring amino acids, optionally alpha-carboxyl esterified oramidated with alkyl or aralkyl of 1 to 12 carbonatoms, preferably 2 to 6 carbon atoms and X is R3-L or D-His (R4)-R5 where R3is void or .omega.-aminoacyl with 1 to 12 carbonatoms, preferably 2 to 6 carbon atoms, R4 is void or imidazole modificationwith alkyl-sulphydryl, hydroxyl, halogen and/oramino groups; and R5 is void or carbonyl (alkyl) amides with 1 to 12 carbonatoms, preferably 2 to 6 carbon atoms.Preferably, the compound is carnosine.
机译:本发明提供了一种治疗并发症的方法和糖尿病的病理。方法涉及将包含以下成分的组合物给予糖尿病受试者选自以下的化合物:(β-Ala-His)n,(Lys-His)n,式R1-X-R2的化合物,其药学上可接受的盐及其组合其中和药学上可接受的载体,其中n是2-5,R1是一两个天然氨基酸任选被1至12个碳的烷基或芳烷基乙酰化的α-氨基原子,优选2至6个碳原子,R2为1或2天然存在的氨基酸,可选地被α-羧基酯化或被1至12个碳的烷基或芳烷基酰胺化原子,优选为2至6个碳原子,X为R3-L或D-His(R4)-R5,其中R3是空的或具有1至12个碳的ω-氨基酰基原子,优选2到6个碳原子,R4为空或咪唑改性带有烷基硫氢基,羟基,卤素和/或氨基;并且R5是空的或具有1至12个碳的羰基(烷基)酰胺原子,优选2至6个碳原子。优选地,该化合物是肌肽。

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