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(2S,3R,4S,5S,6R)-2-(4-chloro-3-(4-methoxybenzyl)phenyl)-6-(hydroxymethyl)-2-hydroxytetrahydro-2H-pyran-3,4,5-triol

中文名称
——
中文别名
——
英文名称
(2S,3R,4S,5S,6R)-2-(4-chloro-3-(4-methoxybenzyl)phenyl)-6-(hydroxymethyl)-2-hydroxytetrahydro-2H-pyran-3,4,5-triol
英文别名
(2S,3R,4S,5S,6R)-2-[4-chloro-3-[(4-methoxyphenyl)methyl]phenyl]-6-(hydroxymethyl)oxane-2,3,4,5-tetrol
(2S,3R,4S,5S,6R)-2-(4-chloro-3-(4-methoxybenzyl)phenyl)-6-(hydroxymethyl)-2-hydroxytetrahydro-2H-pyran-3,4,5-triol化学式
CAS
——
化学式
C20H23ClO7
mdl
——
分子量
410.851
InChiKey
TXCSXLVWVBVQDJ-OBKDMQGPSA-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):
    1.2
  • 重原子数:
    28
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    120
  • 氢给体数:
    5
  • 氢受体数:
    7

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • D-xylopyranosyl-substituted phenyl derivatives, medicaments containing such compounds, their use and process for their manufacture
    申请人:Eckhardt Matthias
    公开号:US20060009400A1
    公开(公告)日:2006-01-12
    A D-Xylopyranosyl-substituted phenyl compound of general formula I wherein the groups R 1 to R 5 , X, Z and R 7a , R 7b , R 7c are defined as in claim 1, have an inhibiting effect on the sodium-dependent glucose cotransporter SGLT. The present invention also relates to pharmaceutical compositions for the treatment of metabolic disorders.
    一般公式I中的A D-吡喃木糖基取代的苯基化合物 其中,R1至R5、X、Z以及R7a、R7b、R7c的定义如权利要求1所述,对钠依赖性葡萄糖共转运体SGLT具有抑制作用。本发明还涉及用于治疗代谢性疾病的药物组合物。
  • PROCESSES FOR THE PREPARATION OF SGLT-2 INHIBITORS, INTERMEDIATES THEREOF
    申请人:EMMENNAR PHARMA PRIVATE LIMITED
    公开号:US20200331946A1
    公开(公告)日:2020-10-22
    The present invention relates to modified, improved processes for the preparation of sodium glucose co-transporter 2 (SGLT-2) inhibitors and intermediates thereof. More particularly, the present invention relates to improved processes for the preparation of gliflozin compounds such as empagliflozin and dapagliflozin, intermediates thereof. The product obtained from the processes of present invention may be amorphous or crystalline. Also, the products obtained from the present invention may be used for the preparation of medicaments for the prevention and/or treatment of diseases and conditions associated with SGLT-2 inhibition.
    本发明涉及改进的,用于制备钠葡萄糖共转运体2(SGLT-2)抑制剂及其中间体的过程。更具体地,本发明涉及用于制备格列凡诺类化合物,如恩帕格列凡诺和达帕格列凡诺及其中间体的改进过程。本发明所得到的产物可以是非晶态或晶态。此外,本发明所得到的产物可用于制备药物,用于预防和/或治疗与SGLT-2抑制有关的疾病和症状。
  • Glucopyranosyl-substituted benzonitrile derivatives, pharmaceutical compositions containing such compounds, their use and process for their manufacture
    申请人:Eckhardt Matthias
    公开号:US20080058379A1
    公开(公告)日:2008-03-06
    Glucopyranosyl-substituted benzonitrile derivatives as defined herein, including the tautomers, the stereoisomers thereof, the mixtures thereof and the salts thereof. The compounds according to the invention are suitable for the treatment of metabolic disorders.
    本发明涉及一种葡萄糖吡喃基取代的苯甲腈衍生物,包括其互变异构体、立体异构体、混合物和盐。本发明所述化合物适用于治疗代谢性疾病。
  • Process for the preparation of D-glucitol, 1,5-anhydro-1-C-[4-chloro-3-[[4-[[(3S)-tetrahydro-3-furanyl] oxy]phenyl] methyl] phenyl]-, (1S) and its crystalline forms thereof
    申请人:MSN LABORATORIES PRIVATE LIMITED
    公开号:US10913762B2
    公开(公告)日:2021-02-09
    The present invention relates to process for the preparation of D-glucitol, 1,5-anhydro-1-C-[4-chloro-3-[[4-[[(3S)-tetrahydro-3-furanyl]oxy]phenyl] methyl]phenyl]-, (1S) formula-1 and its crystalline forms thereof.
    本发明涉及 D-葡萄糖醇、1,5-脱水-1-C-[4-氯-3-[[4-[[(3S)-四氢-3-呋喃基]氧基]苯基]甲基]苯基]-、(1S)式-1 及其结晶形式的制备工艺。
  • D-XYLOPYRANOSYL-SUBSTITUIERTE PHENYLE, DIESE VERBINDUNGEN ENTHALTENDE ARZNEIMITTEL, DEREN VERWENDUNG UND VERFAHREN ZU IHRER HERSTELLUNG
    申请人:BOEHRINGER INGELHEIM INTERNATIONAL GMBH
    公开号:EP1765842B1
    公开(公告)日:2008-01-09
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