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

达格列净杂质19 | 1469910-84-6

中文名称
达格列净杂质19
中文别名
——
英文名称
EM2U3W3Ack
英文别名
[(2R)-2-acetyloxy-2-[(2R,3S,4S,5S)-3,4-diacetyloxy-5-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]oxolan-2-yl]ethyl] acetate
达格列净杂质19化学式
CAS
1469910-84-6
化学式
C29H33ClO10
mdl
——
分子量
577.028
InChiKey
DDGUSZPVZCBVHM-ZCCUTQAASA-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):
    4.13
  • 重原子数:
    40.0
  • 可旋转键数:
    11.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    123.66
  • 氢给体数:
    0.0
  • 氢受体数:
    10.0

反应信息

  • 作为反应物:
    描述:
    达格列净杂质19sodium methylate 作用下, 以 甲醇 为溶剂, 反应 3.0h, 以97%的产率得到(1S)-1,4-anhydro-1-[4-chloro-3-(4-ethoxybenzyl)phenyl]-D-glucitol
    参考文献:
    名称:
    Synthesis and biological evaluation of novel C-aryl d-glucofuranosides as sodium-dependent glucose co-transporter 2 inhibitors
    摘要:
    Novel C-aryl-D-glucofuranosides were synthesized and evaluated for their capacity to inhibit human sodium-dependent glucose co-transporter 2 (hSGLT2) and hSGLT1. Compound 21q demonstrated the best in vitro inhibitory activity against SGLT2 in this series (EC50 = 0.62 mu M). (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2013.08.067
  • 作为产物:
    参考文献:
    名称:
    Synthesis and biological evaluation of novel C-aryl d-glucofuranosides as sodium-dependent glucose co-transporter 2 inhibitors
    摘要:
    Novel C-aryl-D-glucofuranosides were synthesized and evaluated for their capacity to inhibit human sodium-dependent glucose co-transporter 2 (hSGLT2) and hSGLT1. Compound 21q demonstrated the best in vitro inhibitory activity against SGLT2 in this series (EC50 = 0.62 mu M). (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2013.08.067
点击查看最新优质反应信息