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2-Deoxy-DL-ribo-hexopyranose | 61-58-5

中文名称
——
中文别名
——
英文名称
2-Deoxy-DL-ribo-hexopyranose
英文别名
(4R,5R)-6-(hydroxymethyl)oxane-2,4,5-triol
2-Deoxy-DL-ribo-hexopyranose化学式
CAS
61-58-5;13299-15-5;13299-16-6;14215-77-1;14215-78-2;20789-85-9;23568-30-1;25494-04-6;34339-39-4;34339-40-7;34339-46-3;34339-47-4;114717-20-3;114717-21-4;137491-75-9;137491-76-0
化学式
C6H12O5
mdl
——
分子量
164.158
InChiKey
PMMURAAUARKVCB-YLZRJQLMSA-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

物化性质

  • 熔点:
    175 °C
  • 沸点:
    411.0±45.0 °C(Predicted)
  • 密度:
    1.533±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -1.6
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    90.2
  • 氢给体数:
    4
  • 氢受体数:
    5

SDS

SDS:4b091a4d5b5da81ae27a8f19dafb6a20
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文献信息

  • COMPOSITIONS AND METHODS
    申请人:Ionis Pharmaceuticals, Inc.
    公开号:EP2992097B1
    公开(公告)日:2019-11-06
  • Process for the preparation of 1-chloro-3,5-di-o-acyl-2-deoxy-l-ribofuranoside derivatives
    申请人:Tamerlani Giancarlo
    公开号:US20070083041A1
    公开(公告)日:2007-04-12
    Herein described is a process for the preparation of 1-chloro-3,5-di-O-acyl-2-de-oxy-L-ribofuranoside derivatives of general formula (I) useful as intermediates in processes for preparing nucleotides of the L series having antiviral activity.
  • NEOGLYCORANDOMIZATION AND DIGITOXIN ANALOGS
    申请人:Langenhan Joseph M.
    公开号:US20090075842A1
    公开(公告)日:2009-03-19
    The present invention provides methods of producing libraries of compounds with enhanced desirable properties and diminished side effects as well as the compounds produced by the methods. In preferred embodiments, methods of the present invention use a universal chemical glycosylation method that employs reducing sugars and requires no protection or activation. In a preferred embodiment, the invention provides a library of neoglycoside digitoxin analogs that includes compounds with significantly enhanced cytotoxic potency toward human cancer cells and tumor-specificity, but are less potent Na + /K + -ATPase inhibitors in a human cell line than digitoxin.
  • CHEMOENZYMATIC SYNTHESIS OF HEPARIN AND HEPARAN SULFATE ANALOGS
    申请人:The Regents of the University of California
    公开号:US20170016040A1
    公开(公告)日:2017-01-19
    The present invention provides a one-pot multi-enzyme method for preparing UDP-sugars from simple sugar starting materials. The invention also provides a one-pot multi-enzyme method for preparing oligosaccharides from simple sugar starting materials.
  • US7361745B2
    申请人:——
    公开号:US7361745B2
    公开(公告)日:2008-04-22
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