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Novel Iridoid Derivatives That Inhibit Replication of Hepatitis B Virus and Methods for Preparing the Iridoid Derivatives

机译:抑制乙型肝炎病毒复制的新型鸢尾衍生物及其制备方法

摘要

The present invention relates to novel iridoide derivatives of the general formula (I), pharmaceutically acceptable salts and isomers thereof which inhibit the replication of hepatitis B virus.;Where Represents a double bond or a single bond, R 1 represents hydroxy or lower alkoxy, R 2 is formyl; C 1 -C 5 aryl unsubstituted or substituted by one member selected from the group consisting of chloro, azido, substituted or unsubstituted amino, phenylthio or hydroxyimino; C 2 -C 5 alkenyl substituted or unsubstituted by ethoxycarbonyl or phenyl, or R 1 and R 2 together or Group, where n represents an integer from 0 to 2 and R 3 represents hydroxy, acetoxy or C 1 -C 5 alkyl.;The present invention also relates to a method for preparing a compound of formula (I) and a pharmaceutical composition which can be used for the treatment of hepatitis B by containing the compound as an active ingredient.
机译:本发明涉及抑制乙型肝炎病毒复制的通式(I)的新的铱化合物,其药学上可接受的盐和异构体。其中R 1代表双键或单键,R 1 代表羟基或低级烷氧基,R 2 为甲酰基;未被取代或被选自氯,叠氮基,取代或未取代的氨基,苯硫基或羟基亚氨基的一个成员取代的C 1 -C 5 芳基;由乙氧基羰基或苯基或R 1 和R 2 一起取代或未取代的C 2 -C 5 烯基或基团,其中n代表0至2的整数,R 3 代表羟基,乙酰氧基或C 1 -C 5 烷基。本发明还涉及制备式(I)化合物的方法和药物组合物,其通过包含该化合物作为活性成分可用于治疗乙型肝炎。

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