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5-[4-[2-(4-oxo-3,4-dihydro-2H-1,3-benzoxazin-3-yl)ethoxy]benzyl]-2,4-thiazolidinedione | 194713-46-7

中文名称
——
中文别名
——
英文名称
5-[4-[2-(4-oxo-3,4-dihydro-2H-1,3-benzoxazin-3-yl)ethoxy]benzyl]-2,4-thiazolidinedione
英文别名
5-[[4-[2-(4-oxo-2H-1,3-benzoxazin-3-yl)ethoxy]phenyl]methyl]-1,3-thiazolidine-2,4-dione
5-[4-[2-(4-oxo-3,4-dihydro-2H-1,3-benzoxazin-3-yl)ethoxy]benzyl]-2,4-thiazolidinedione化学式
CAS
194713-46-7
化学式
C20H18N2O5S
mdl
——
分子量
398.439
InChiKey
RFMNEXVCPAPDRA-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3
  • 重原子数:
    28
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    110
  • 氢给体数:
    1
  • 氢受体数:
    6

文献信息

  • Benzoazine derivative or salt thereof and pharmaceutical composition comprising the same
    申请人:SS Pharmaceutical Co., Ltd.
    公开号:EP0787727A1
    公开(公告)日:1997-08-06
    A benzoazine derivative represented by the following formula (1),    wherein R1 represents an alkyl group, alkoxy group, halogen atom, halogenoalkyl group, amino group, hydroxy group, benzyloxy group which may have a substituent, cyano group, carbamoyl group, acyl group, nitro group, carboxy group, or sulfonamide group; R2 and R3 may be the same or different and each individually represents a hydrogen atom or an alkyl group, or R2 and R3 indicate in combination an alkylene group having 2-7 carbon atoms; R4 and R5 may be the same or different and each individually represents a hydrogen atom or an alkyl group; X denotes O, S, or N-R6 (wherein R6 represents a hydrogen atom, an alkyl group, or an aryl group or pyridyl group which may have a substituent); m is an integer from 0 to 4; and n is an integer from l to 3, or a salt of the benzoazine derivative. The compound exhibits superior effects for reducing blood glucose value, plasma insulin value, and plasma triglyceride value, and is useful as a medicament for preventing or treating diabetes, hyperlipidemia, and obesity.
    由下式(1)代表的苯并嗪衍生物、 其中 R1 代表烷基、烷氧基、卤素原子、卤代烷基、氨基、羟基、可能具有取代基的苄氧基、氰基、氨基甲酰基、酰基、硝基、羧基或磺酰胺基;R2 和 R3 可以相同或不同,各自单独代表氢原子或烷基,或 R2 和 R3 组合表示具有 2-7 个碳原子的亚烷基;R4和R5可以相同或不同,各自代表氢原子或烷基;X表示O、S或N-R6(其中R6代表氢原子、烷基或芳基或吡啶基,可具有取代基);m是0至4的整数;n是l至3的整数,或苯并嗪衍生物的盐。该化合物在降低血糖值、血浆胰岛素值和血浆甘油三酯值方面表现出卓越的效果,可用作预防或治疗糖尿病、高脂血症和肥胖症的药物。
  • PROPHYLACTIC AGENT AND/OR THERAPEUTIC AGENT FOR CATARACT, MEDICINAL COMPOSITION FOR PREVENTING AND/OR TREATING CATARACT, USE OF PPAR ACTIVATOR FOR PRODUCING SAME, AND EYEDROPS
    申请人:University of Fukui
    公开号:EP3733203A1
    公开(公告)日:2020-11-04
    Provided are agents for prevention and therapeutic treatment of cataract that act by a different mechanism from conventional agents, and use of a PPAR activator for production of such agents. An agent for prevention and/or therapeutic treatment of cataract, containing a PPAR activator as an active ingredient, is used.
    本发明提供了预防和治疗白内障的药剂,其作用机理与传统药剂不同,还提供了使用 PPAR 激活剂生产此类药剂的方法。一种用于预防和/或治疗白内障的药剂含有 PPAR 激活剂作为活性成分。
  • Alpha-Substituted phenylpropionic acid derivative and medicine containing the same
    申请人:SSP Co., Ltd.
    公开号:EP0903343B1
    公开(公告)日:2003-05-28
  • [EN] PPAR-ALPHA AGONISTS FOR TREATING MITOCHONDRIAL DISEASES<br/>[FR] AGONISTES DU RÉCEPTEUR PPAR-ALPHA POUR LE TRAITEMENT DE MALADIES MITOCHONDRIALES
    申请人:MITOBRIDGE INC
    公开号:WO2017044551A1
    公开(公告)日:2017-03-16
    Provided herein are methods for increasing PPARalpha activity and methods for treating PPARalpha related diseases (e.g., mitochondrial diseases).
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