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Superoxide dismutase derivatives, process for their preparation and their use as medicines.

机译:超氧化物歧化酶衍生物,其制备方法及其作为药物的用途。

摘要

The invention provides a superoxide dismutase derivative of the general formula [SOD] [Z]n wherein [SOD] represents a superoxide dismutase having 1 to 22 or 24 groups each derived from an amino group by removal of one hydrogen atom in lieu of amino groups; [Z] represents a monovalent copolymer group, constituting units of which are a group of the formula CHEM wherein R1, R2, R3 and R4 each represents a hydrogen atom or a residue derived by removal of a hydroxyl group from an alkanol of 1 to 8 carbon atoms, an ethylene glycol monoalkyl ether containing an alkyl moiety of 1 to 4 carbon atoms or a glycerin dialkyl ether containing alkyl moieties of 1 to 4 carbon atoms, provided that either R1 or R2 and either R3 or R4 each represents a hydrogen atom, and a residue derived from the group of the above-mentioned formula by removal of OR1, OR2, OR3 or OR4 group from one of its COOR1, COOR2, COOR3 and COOR4 groups (where the bond on the carbon atom of the carbonyl group is attached to [SOD]), said monovalent copolymer group having an average molecular weight of 500 to 200,000; and n represents an integer of 1 to 22 or 24 corresponding to the number of said groups each derived from an amino group by removal of one hydrogen atom in said [SOD], or a pharmaceutically acceptable salt thereof. There also is provided a method for producing the above derivative and salt. The invention is further directed to medicinal uses and pharmaceutical compositions for oral administration.
机译:本发明提供了通式[SOD] [Z] n的超氧化物歧化酶衍生物,其中[SOD]代表具有1-22或24个基团的超氧化物歧化酶,每个基团均通过除去一个氢原子代替氨基而衍生自氨基; [Z]表示一价共聚物基团,其构成单元是式的基团,其中R 1,R 2,R 3和R 4各自表示氢原子或残基通过从具有1至8个碳原子的烷醇中除去羟基而得到,含有1至4个碳原子的烷基部分的乙二醇单烷基醚或具有1至4个碳原子的烷基部分的甘油二烷基醚,条件是R 1或R 2以及R 3或R 4分别表示氢原子,以及通过去除OR 1,OR 2衍生自上述式的基团的残基。来自其COOR 1,COOR 2,COOR 3和COOR 4之一的羰基上的>,OR 3或OR 4基(其中羰基的碳原子上的键连接至[SOD]),所述一价共聚物基团的平均分子量为500至200,000; n表示1〜22或24的整数,其与通过除去所述[SOD]中的一个氢原子而各自衍生自氨基的所述基团的数目或其药学上可接受的盐相对应。还提供了制备上述衍生物和盐的方法。本发明进一步涉及用于口服的药物用途和药物组合物。

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