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Substituted 1-aza-2-imino-heterocycles and their use as nicotinic acetylcholin receptors activators

机译:取代的1-氮杂-2-亚氨基杂环化合物及其作为烟碱乙酰胆碱受体激活剂的用途

摘要

There is provided heterocyclic compounds of the following formula (I): chemistry chemdraw filechemistry mol file;in which, ;A is optionally substituted alkyl group, optionally substituted aryl group or optionally substituted heterocyclic group; ;B1 and B2 are, hydrogen atom, alkyl group or hydroxyl group; or combined together to represent carbonyl group; ;X is oxygen atom, sulfur atom, carbon atom or nitrogen atom; ;dotted line shows either presence or absence of bond; ;n is integer of 1 or 2; and ;the group XY represents optionally substituted alkylene or cyclic alkenylene bond; ;or a pharmaceutically acceptable salt thereof. ;These compounds have good affinity for 42 nicotinic acetylcholine receptors and activate the same to thereby exert a preventive or therapeutic effect on cerebral dysfunction.
机译:提供了下式(I)的杂环化合物: <图像文件=“ US20030134848A1-20030717-C00001.GIF” he =“ 61.43445” imgContent =“ undefined” imgFormat =“ GIF” wi =“ 157.2291” /> 化学chemdraw文件 化学mol文件< / ExternalFileRef> ;其中,; A是任选取代的烷基,任选取代的芳基或任选取代的杂环基; ; B 1 和B 2 是氢原子,烷基或羟基;或结合在一起代表羰基; X是氧原子,硫原子,碳原子或氮原子;虚线表示存在或不存在键; ; n是1或2的整数; ;和;基团XY代表任选取代的亚烷基或环状亚烯键。 ;或其药学上可接受的盐。 ;这些化合物对42种烟碱乙酰胆碱受体具有良好的亲和力,并激活它们,从而对脑功能障碍发挥预防或治疗作用。

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