摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1-[2-(4-{3-[2-hydroxy-1,1-bis(hydroxymethyl)ethyl-amino]propoxy}phenyl)ethyl]-7-(2,3,4,6-tetra-O-pivaloyl-β-D-glucopyranosyloxy)-1H-indole

中文名称
——
中文别名
——
英文名称
1-[2-(4-{3-[2-hydroxy-1,1-bis(hydroxymethyl)ethyl-amino]propoxy}phenyl)ethyl]-7-(2,3,4,6-tetra-O-pivaloyl-β-D-glucopyranosyloxy)-1H-indole
英文别名
[(2R,3R,4S,5R,6S)-6-[1-[2-[4-[3-[[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]amino]propoxy]phenyl]ethyl]indol-7-yl]oxy-3,4,5-tris(2,2-dimethylpropanoyloxy)oxan-2-yl]methyl 2,2-dimethylpropanoate
1-[2-(4-{3-[2-hydroxy-1,1-bis(hydroxymethyl)ethyl-amino]propoxy}phenyl)ethyl]-7-(2,3,4,6-tetra-O-pivaloyl-β-D-glucopyranosyloxy)-1H-indole化学式
CAS
——
化学式
C49H72N2O14
mdl
——
分子量
913.116
InChiKey
MAXFOTCTOCOUDE-HRSAFRLBSA-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):
    6.8
  • 重原子数:
    65
  • 可旋转键数:
    27
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.63
  • 拓扑面积:
    211
  • 氢给体数:
    4
  • 氢受体数:
    15

反应信息

点击查看最新优质反应信息

文献信息

  • 1-SUBSTITUTED-7-(B-D-GLYCOPYRANOSYLOXY)(AZA)INDOLE COMPOUND AND PHARMACEUTICAL CONTAINING THE SAME
    申请人:Fushimi Nobuhiko
    公开号:US20090054356A1
    公开(公告)日:2009-02-26
    [Objective] The present invention provides a compound having an SGLT1 and/or SGLT2 inhibitory activity which is usable as an agent for the prevention or treatment of diabetes, postprandial hyperglycemia, impaired glucose tolerance, diabetic complications, obesity or the like. [Means to Solve the Problem] It is a 1-substituted-7-(β-D-glycopyranosyloxy)(aza)-indole compound represented by the general formula (I), a prodrug thereof, or a pharmaceutically acceptable salt thereof, or a hydrate or solvate thereof: wherein R 1 represents a halogen atom or the like; n represents j an integer number from 0 to 3; R 2 represents a hydrogen atom or the like; X represents a carbon atom which a hydrogen atom or the like binds to, or a nitrogen atom; Q represents an alkylene group or an alkenylene group each of which may have an oxygen atom or a sulfur atom in the chain; and A represents an aryl or heteroaryl group which may have a substituent.
    【目的】本发明提供一种具有SGLT1和/或SGLT2抑制活性的化合物,可用作预防或治疗糖尿病、餐后高血糖、糖耐量受损、糖尿病并发症、肥胖症等的药物。 【解决问题的手段】化合物为1-取代-7-(β-D-葡萄糖苷基氧)(氮杂)吲哚化合物,由通式(I)表示,其前药、药学上可接受的盐、水合物或溶剂化物:其中R1表示卤素原子或类似物;n表示0至3的整数;R2表示氢原子或类似物;X表示与碳原子结合的氢原子或类似物,或氮原子;Q表示可在链中具有氧原子或硫原子的烷基或烯基;A表示可能具有取代基的芳基或杂芳基。
  • US7749972B2
    申请人:——
    公开号:US7749972B2
    公开(公告)日:2010-07-06
  • 1-SUBSTITUTED-7-( -D-GLYCOPYRANOSYLOXY)(AZA)INDOLE COMPOUND AND PHARMACEUTICAL CONTAINING THE SAME
    申请人:Kissei Pharmaceutical Co., Ltd.
    公开号:EP1849795B1
    公开(公告)日:2011-01-26
查看更多