首页> 外国专利> PYRIDINE THIODIVENCY AND PHARMACEUTICAL COMPOSITION THAT CONTAINS AND HAS THE ABILITY TO ACT AGAINST HELICOBACTER PYLORI

PYRIDINE THIODIVENCY AND PHARMACEUTICAL COMPOSITION THAT CONTAINS AND HAS THE ABILITY TO ACT AGAINST HELICOBACTER PYLORI

机译:含有并具有抗幽门螺杆菌作用的吡啶类生物活性和药物成分

摘要

1. The pyridine thio derivative represented by the following general formula (I), or a pharmacologically acceptable salt thereof: wherein R and R respectively represent a hydrogen atom, a C1-6 alkyl group, a C1-6 alkoxy group or a halogen atom; R and R respectively represent a hydrogen atom, a C1-6 alkyl group or a C1-4 alkoxy group; X represents —O—, —S— or —NH—; Y represents a C1-6 alkyl group which may be substituted by a substituent selected from the group consisting of a hydroxyl group, a C1-6 alkoxy group and a halogen atom, or - (RO) -R (where R represents a C1-6 alkylene group, R represents a C1-6 alkyl group which may be substituted by a substituent selected from a group consisting of a hydroxyl group, a C 1 alkoxy group and a halogen atom, and n is an integer from 1 to 10) and Z represents a hydrogen atom or C 1 alkyl group. 2. The thyroid derivative of pyridine or a pharmacologically acceptable salt thereof according to claim 1, wherein Y in the general formula (I) is a C1-6 alkyl group which may be substituted with a substituent selected from the group consisting of a hydroxyl group or a C1-4 alkoxy group. The pyridine thio derivative or a pharmacologically acceptable salt thereof according to claim 1, wherein Y in the general formula (I) is - (RO) -R (where R represents a C1-6 alkylene group, R represents a C1-6 alkyl group which may be substituted with a substituent selected from the group consisting of hydroxyl groups, alkoxy groups and halogen atoms, and n is an integer from 1 to 10), where R is an ethylene group and R is a C1-6 alkyl group which may be substituted by a fluorine atom. 4. The thyroid derivative of pyridine or a pharmacologically acceptable salt thereof according to any one of the preceding claims 1 to 3, where X in the general formula (I) means —O— or —S — .5.
机译:1.由以下通式(I)表示的吡啶硫代衍生物或其药理学上可接受的盐:其中R 1和R 2分别代表氢原子,C 1-6烷基,C 1-6烷氧基或卤素原子。 ; R和R分别代表氢原子,C1-6烷基或C1-4烷氧基; X代表-O-,-S-或-NH-; Y代表可被选自羟基,C1-6烷氧基和卤素原子或-(RO)-R(其中R表示C1- R 6为亚烷基,R表示可被选自羟基,C 1烷氧基和卤素原子的组中的取代基取代的C 1-6烷基,n为1〜10的整数。 Z表示氢原子或C 1烷基。 2.根据权利要求1的吡啶的甲状腺衍生物或其药理学上可接受的盐,其中通式(I)中的Y为可被选自羟基的取代基取代的C1-6烷基。或C 1-4烷氧基。 2.根据权利要求1所述的吡啶硫代衍生物或其药理学上可接受的盐,其中,通式(I)中的Y为-(RO)-R(其中,R表示碳原子数1〜6的亚烷基,R表示碳原子数1〜6的烷基。可以被选自羟基,烷氧基和卤素原子的取代基取代,并且n是1至10的整数),其中R是亚乙基,R是C1-6烷基,被氟原子取代。 4.根据前述权利要求1至3中任一项的吡啶的甲状腺衍生物或其药理学可接受的盐,其中通式(I)中的X是-O-或-S-.5。

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