首页> 外国专利> PPAR-GAMMA AGONISTS FOR THE INDUCTION OF CATIONIC ANTIMICROBIAL PEPTIDE EXPRESSION AS IMMUNOPROTECTIVE STIMULANTS

PPAR-GAMMA AGONISTS FOR THE INDUCTION OF CATIONIC ANTIMICROBIAL PEPTIDE EXPRESSION AS IMMUNOPROTECTIVE STIMULANTS

机译:PPAR-γ激动剂,可诱导阳离子抗菌肽作为免疫保护性表达

摘要

Rosiglitazone, 5-ASA or structurally analagous compounds according to the general formula (1): FORMULA in which R1 and R2 which maybe identical or different, are selected from the group comprising -H or a linear or branched alkyl group having from 1 to 6 carbon atoms or tegether form an aromatic or aliphatic ring with 5 or 6 atoms; Y and Z, which may be identical or different, are selected from the group comprising -H, -OH, -COOH, in which R3 is selected from H, phenyl, benzyl, -CF3 or -CF2CF3, vinyl, allyl and a linear or branched alkyl group having from 1 to 6 carbon atoms; or compounds or according to the general formula (Ia); FORMULA in which R1 and R2, which may be identical or defferent, are selected from the group comprising H, -CnH2n-1, where n= 1-6, a linear or branched aldyl group having from 1 to 6 carbon atoms, or together form an aromatic or apiphatic ring with 5 or 6 atoms; R3 is selected from -CO-CH, -NHOH, -OH, -OR6 in which R6 is a linear or branched alkyl group having from 1 to 6 carbon atoms; R3 is selected from -CO-CH, -NHOH, -OH, -OR6 in which R6 is a linear or branched alkyl group having from 1 to 6 carbon atoms; R4 is selected from H, a linear or branched alkyl group having from 1 to 6 carbon atoms, phenyl, benxyl, -CF3 or -CF2CF3 vinyl or allyl; R5, R7, R8 are hydrogen atoms; or R3 and R4, R4 and R5, or R7 and R8 together form a ring, fused to the benzene, aromatic or aliphatic ring with 5 or 6 atoms comprising from 1 to 2 heteroatoms selected independently from the group comprising N, O; in the induction of CAMP expression in the gut.
机译:罗格列酮,5-ASA或通式(1)的结构类似化合物:其中R1和R2相同或不同,选自-H或具有1或1的直链或支链烷基至6个碳原子或叔醚形成具有5或6个原子的芳族或脂族环; Y和Z可以相同或不同,选自-H,-OH,-COOH,其中R 3选自H,苯基,苄基,-CF 3或-CF 2 CF 3,乙烯基,烯丙基和直链。或具有1-6个碳原子的支链烷基;或或化合物或根据通式(Ia); <式>,其中R 1和R 2可以相同或不同,选自H,-CnH 2n-1,其中n = 1-6,具有1至6个碳原子的直链或支链的醛基,或一起形成具有5或6个原子的芳族或脂族环; R3选自-CO-CH,-NHOH,-OH,-OR6,其中R6是具有1-6个碳原子的直链或支链烷基。 R3选自-CO-CH,-NHOH,-OH,-OR6,其中R6是具有1-6个碳原子的直链或支链烷基。 R4选自H,具有1-6个碳原子的直链或支链烷基,苯基,苄基,-CF3或-CF2CF3乙烯基或烯丙基; R5,R7,R8为氢原子;或R 3和R 4,R 4和R 5或R 7和R 8一起形成环,稠合至具有5或6个原子的苯,芳族或脂族环,所述原子包含1至2个独立地选自N,O的杂原子;或在肠道中诱导CAMP表达。

著录项

  • 公开/公告号HRP20120473T1

    专利类型

  • 公开/公告日2012-07-31

    原文格式PDF

  • 申请/专利权人 GIULIANI INTERNATIONAL LIMITED;

    申请/专利号HR2012P000473T

  • 申请日2012-06-05

  • 分类号A61K31/136;A61K31/166;A61K31/196;A61K31/343;A61K31/357;A61K31/4439;A61K31/47;A61K31/606;A61K31/609;A61P1;A61P1/02;A61P1/04;A61P11/02;A61P17;G01N33/94;

  • 国家 HR

  • 入库时间 2022-08-21 17:24:54

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