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Arilmetilaminas replaced, Pharmaceutical compositions and Use thereof for the manufacture of a medicament

机译:取代了阿里米特米那斯,药物组合物及其在制造药物中的用途

摘要

The alternative arilmethamine includes a formula compound (1),wherein Ar is an aryl group or a heteroaryl group, and the group of formula (2) is beta with respect to the group of formula (3),In arilo: the dividing line is a simple or double-sided link; R1 and R2 are independent hydrogen or low tar; R3 is arilo, arilalquenilo, cyclo cycloquilo, cycloquilo, heteromorphous, heteromorphous, heteromorphous alquenilo, heterocyclopropene, An isocyclic compound associated with carbon or alternative tar consisting of one or more hydroxyl, alcoxi, acrylonitrile, cyclopropyl, isocyclic, R6, - or6, - S (o) mr6 O-C (= O) - R6; R4 is hydrogen, acid, alcox, hydrocarbon, carbon, cyanogen, halogen, hydrogen, -C (= O) - ny1y2, or alternative asphalt such as Alcoy, lcarbonilamine, polyfonilamino, hydroxi, - S (o) m-codilo-ny1y2;R5 is hydrogen, acyl, alkoxy, alkyloxycarbonyl, aryl, carboxy, cyano, halo, heteroaryl, heteroaryloxy, heterocycloalkyl, heterocycloalkyloxy, heterocycloalkylalkyl, heteroarylalkyloxy, hydroxy, trifluoromethyl, -C (= O) -NY1Y2, -NZ1-C, -6alkylene-R7 or alkyl optionally substituted with alkoxy, alkylcarbonylamino, alkylsulfonylamino, aryl, heteroaryl, heterocycloalkyl, hydroxy, ureido, -C (= O) -NY1Y2, -SO2-NY1Y2, -S (O) m-alkyl or -NY1Y2 ; R6 is aryl or heteroaryl; R7 is hydroxy, alkoxy, ureido, -C (= O) -NY1Y2, -SO2-NY1Y2, -S (O) m-alkyl or -NY1Y2; R8 is hydrogen or lower alkyl; Y1 and Y2 are independently hydrogen, alkenyl, alkyl, aryl, arylalkyl,Cyclopropyl, heteromorphic, heteromorphic, heteromorphic or heteromorphic cyclopropyl or class ii-ny1y2 can form a periodic ammonia water; Z1 is O (o) m or nr8; m is zero or 1-2 integer; n is zero or 1-4 integer; n-oxidizes this compound, the product of this compound, the drug acceptable salt of this compound, a solution This compound and the hydrate of this compound have triploid inhibitory activity, including the pharmaceutical components of these compounds, and the use of these compounds to make drugs to treat patients with conditions and diseases,Or a disorder that can be improved by using triple velocity inhibitors, such as asthma and inflammation, to name just a few.
机译:替代的阿立次胺包括式化合物(1),其中Ar是芳基或杂芳基,并且式(2)的基团相对于式(3)的基团是β。简单或双面链接; R1和R2是独立的氢或低焦油; R 3是芳基,芳基喹啉基,环环基喹啉基,环基吡咯基,杂晶,杂晶,杂晶铝基,杂环丙烯,与碳缔合的杂环化合物或由一个或多个羟基,醇,丙烯腈,环丙基,杂环基,R 6,-或6-,-组成的替代焦油。 S(o)mr6 OC(= O)-R6; R4是氢,酸,醇,烃,碳,氰,卤素,氢,-C(= O)-ny1y2或其他沥青,例如Alcoy,lcarbilamine,polyfonilamino,hydroxi,-S(o)m-codilo-ny1y2 R5是氢,酰基,烷氧基,烷氧基羰基,芳基,羧基,氰基,卤素,杂芳基,杂芳氧基,杂环烷基,杂环烷氧基,杂环烷基烷基,杂芳基烷氧基,羟基,三氟甲基,-C(= O)-NY1Y2,-NZ1-C,- 6亚烷基-R 7或任选地被烷氧基,烷基羰基氨基,烷基磺酰基氨基,芳基,杂芳基,杂环烷基,羟基,脲基,-C(= O)-NY 1Y 2,-SO 2 -NY 1Y 2,-S(O)间烷基或-NY 1Y 2取代的烷基; R6是芳基或杂芳基; R7是羟基,烷氧基,脲基,-C(= O)-NY1Y2,-SO2-NY1Y2,-S(O)间烷基或-NY1Y2; R8是氢或低级烷基; Y1和Y2独立地是氢,烯基,烷基,芳基,芳基烷基,环丙基,杂晶的,杂晶的,杂晶的或杂晶的环丙基,或ii-ny1y2类可以形成周期性的氨水; Z 1是O(o)m或nr8; m为零或1-2的整数; n为零或1-4的整数; n-氧化该化合物,该化合物的产物,该化合物的药物可接受的盐,溶液该化合物和该化合物的水合物具有三倍体抑制活性,包括这些化合物的药物成分,以及这些化合物的用途制造治疗疾病和疾病患者的药物,或者可以通过使用三倍速抑制剂(例如哮喘和炎症)来改善疾病的药物。

著录项

  • 公开/公告号AR033525A1

    专利类型

  • 公开/公告日2003-12-26

    原文格式PDF

  • 申请/专利权人 AVENTIS PHARMA LIMITED;

    申请/专利号AR2001P102009

  • 发明设计人

    申请日2001-04-27

  • 分类号C07D401/06;C07D401/10;C07D401/12;C07D405/06;C07D405/10;C07D405/14;C07D409/06;C07D409/14;C07D413/10;C07D413/14;C07D417/06;C07D471/04;C07D471/06;C07D487/04;C07D495/04;C07D211/16;A61K31/451;A61K31/4427;A61K31/44;A61K31/435;A61K31/415;A61K31/407;A61K31/4035;A61K31/381;A61K31/352;A61K31/343;A61P43/00;A61P37/00;A61P37/02;A61P35/00;A61P29/00;A61P27/02;A61P19/00;A61P19/02;A61P19/04;A61P19/06;A61P19/10;A61P17/00;A61P17/02;A61P17/04;A61P17/06;A61P11/00;A61P11/06;A61P11/08;A61P11/14;A61P9/00;A61P9/04;A61P9/06;A61P9/08;A61P9/10;A61P7/00;A61P7/12;A61P3/10;

  • 国家 AR

  • 入库时间 2022-08-21 23:12:31

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