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ethyl-arabinofuranoside

中文名称
——
中文别名
——
英文名称
ethyl-arabinofuranoside
英文别名
Aethyl-arabinofuranosid;Ethyl beta-d-riboside;2-ethoxy-5-(hydroxymethyl)oxolane-3,4-diol
ethyl-arabinofuranoside化学式
CAS
——
化学式
C7H14O5
mdl
——
分子量
178.185
InChiKey
XESKOQZTIQOBMT-UHFFFAOYSA-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:
    12
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    79.2
  • 氢给体数:
    3
  • 氢受体数:
    5

文献信息

  • Human helicase DDX3 inhibitors as therapeutic agents
    申请人:AZIENDA OSPEDALIERA UNIVERSITARIA SENESE
    公开号:US10941121B2
    公开(公告)日:2021-03-09
    The present invention refers to compounds endowed with RNA helicase DDX3 inhibitory activity of formula I and II and their therapeutic use, in particular for the treatment of viral diseases.
    本发明是指具有式 I 和 II 的 RNA 螺旋酶 DDX3 抑制活性的化合物及其治疗用途,特别是用于治疗病毒性疾病。
  • Use of DDX3 inhibitors as antiproliferative agents
    申请人:AZIENDA OSPEDALIERA UNIVERSITARIA SENESE
    公开号:US11000512B2
    公开(公告)日:2021-05-11
    The present invention refers to compounds of formula I or II endowed with DDX3 inhibitory activity, relative pharmaceutical compositions and their use as antihyperproliferative agents. (I) or (II).
    本发明涉及具有 DDX3 抑制活性的式 I 或式 II 化合物、相关药物组合物及其作为抗过增殖剂的用途。(I)或(II)。
  • USE OF DDX3 INHIBITORS AS ANTIPROLIFERATIVE AGENTS
    申请人:AZIENDA OSPEDALIERA UNIVERSITARIA SENRESE
    公开号:US20190099403A1
    公开(公告)日:2019-04-04
    The present invention refers to compounds of formula I or II endowed with DDX3 inhibitory activity, relative pharmaceutical compositions and their use as antihyperproliferative agents. (I) or (II)
  • HUMAN HELICASE DDX3 INHIBITORS AS THERAPEUTIC AGENTS
    申请人:AZIENDA OSPEDALIERA UNIVERSITARIA SENESE
    公开号:US20200140398A1
    公开(公告)日:2020-05-07
    The present invention refers to compounds endowed with RNA helicase DDX3 inhibitory activity of formula I and II and their therapeutic use, in particular for the treatment of viral diseases.
  • [EN] USE OF O-GLYCOSYLATED INDOLE OR INDOLINE DERIVATIVE WITH GLYCOSIDASE FOR DEYING KERATIN FIBERS<br/>[FR] UTILISATION D'UN DÉRIVÉ D'INDOLE OU D'INDOLINE O-GLYCOSYLÉ AVEC UNE GLYCOSIDASE POUR COLORER DES FIBRES DE KÉRATINE
    申请人:OREAL
    公开号:WO2017182340A1
    公开(公告)日:2017-10-26
    A subject of the invention is the use of i) hydroxyindol(in)e derivative(s) glycosylated on at least one hydroxyl group, in the presence of at least ii) one enzyme with glycosidase activity, in particular beta-glycosidase activity, more particularly glucosidase activity and even more particularly beta-glucosidase activity, for treating keratin fibres, in particular dyeing human keratin fibres such as the hair, preferably dyeing said fibres. A subject of the invention is also a process for treating keratin fibres using i), ii) and a kit comprising the ingredients i) and ii). The process according to the invention has the advantage of dyeing human keratin fibres, with powerful or chromatic dyeing results that are resistant to washing, perspiration, sebum andlight, and that are moreover long-lasting, without impairing said fibres. Furthermore, the colourations obtained from the process give uniform colours from the root to the tip of a fibre (low colouration selectivity). In addition, the compositions comprising the i) hydroxyindol(in)e derivative(s) glycosylated on at least one of the hydroxyl groups degrade very little in air and remain stable with respect to storage.
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