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O4-methyl-D-6-deoxy-galactose | 6988-38-1

中文名称
——
中文别名
——
英文名称
O4-methyl-D-6-deoxy-galactose
英文别名
(2R,3R,4S,5R)-2,3,5-trihydroxy-4-methoxyhexanal
<i>O</i><sup>4</sup>-methyl-<i>D</i>-6-deoxy-galactose化学式
CAS
6988-38-1
化学式
C7H14O5
mdl
——
分子量
178.185
InChiKey
GCCHQQYEUACPFL-UCROKIRRSA-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):
    -1.8
  • 重原子数:
    12
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    87
  • 氢给体数:
    3
  • 氢受体数:
    5

文献信息

  • Biosynthesis of everninomicin analogs in Micromonospora carbonacea var aurantiaca
    申请人:VANDERBILT UNIVERSITY
    公开号:US10696996B2
    公开(公告)日:2020-06-30
    Disclosed are methods of preparing everninomicin analogs by genetic alteration of Micromonospora carbonacea. Everninomicin analogs prepared by these methods and methods of using these analogs to treat infections are also disclosed.
    本发明公开了通过改变小孢子虫(Micromonospora carbonacea)的基因来制备 Everninomicin 类似物的方法。还公开了通过这些方法制备的常新霉素类似物以及使用这些类似物治疗感染的方法。
  • BIOSYNTHESIS OF EVERNINOMICIN ANALOGS IN MICROMONOSPORA CARBONACEA VAR AURANTIACA
    申请人:Vanderbilt University
    公开号:EP3387133A1
    公开(公告)日:2018-10-17
  • Avilamycin derivatives
    申请人:Combinature Biopharm AG
    公开号:US20040006026A1
    公开(公告)日:2004-01-08
    Avilamycin derivatives, gene technology biosynthesis processes for their production, medications containing these compounds, as well as the use of these compounds for the production of a active agent against infectious diseases, as well as nucleic acids, proteins, and gene clusters and corresponding cells that are connected to the production of these avilamycin derivatives are disclosed.
  • [EN] BIOSYNTHESIS OF EVERNINOMICIN ANALOGS IN MICROMONOSPORA CARBONACEA VAR AURANTIACA<br/>[FR] BIOSYNTHÈSE D'ANALOGUES D'ÉVERNINOMICINE DANS MICROMONOSPORA CARBONACEA VAR AURANTIACA
    申请人:UNIV VANDERBILT
    公开号:WO2017100650A1
    公开(公告)日:2017-06-15
    Disclosed are methods of preparing everninomicin analogs by genetic alteration of Micromonospora carbonacea. Everninomicin analogs prepared by these methods and methods of using these analogs to treat infections are also disclosed.
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