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2-tert-Butoxy-1-morpholin-4-yl-ethanone | 77664-60-9

中文名称
——
中文别名
——
英文名称
2-tert-Butoxy-1-morpholin-4-yl-ethanone
英文别名
2-[(2-methylpropan-2-yl)oxy]-1-morpholin-4-ylethanone
2-tert-Butoxy-1-morpholin-4-yl-ethanone化学式
CAS
77664-60-9
化学式
C10H19NO3
mdl
——
分子量
201.266
InChiKey
IEWLSECOMSFCRF-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):
    0.2
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    38.8
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

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文献信息

  • RENIN INHIBITORS
    申请人:Jones Benjamin
    公开号:US20100210635A1
    公开(公告)日:2010-08-19
    Compounds, pharmaceutical compositions, kits and methods are provided for use with Renin that comprise a compound selected from the group consisting of: wherein the variables are as defined herein.
    提供了用于与Renin一起使用的化合物、药物组合物、试剂盒和方法,其中包括从以下组中选择的化合物:其中变量如本文所定义。
  • Renin inhibitors
    申请人:Jones Benjamin
    公开号:US20090105251A1
    公开(公告)日:2009-04-23
    Compounds, pharmaceutical compositions, kits and methods are provided for use with renin that comprise a compound selected from the group consisting of: wherein the variables are as defined herein.
    提供了与肾素一起使用的化合物、药物组合物、试剂盒和方法,其中包括从以下组中选择的化合物:其中变量如本文所定义。
  • Heteroalkyl-substituted biphenyl-4-carboxylic acid arylamide analogues
    申请人:Hodgetts J. Kevin
    公开号:US20070191363A1
    公开(公告)日:2007-08-16
    Heteroalkyl-substituted biphenyl-4-carboxylic acid arylamide analogues are provided, of the formula: wherein variables are as described herein. Such compounds are ligands that may be used to modulate specific receptor activity in vivo or in vitro, and are particularly useful in the treatment of conditions associated with pathological receptor activation in humans, domesticated companion animals and livestock animals. Pharmaceutical compositions and methods for using such compounds to treat such disorders are provided, as are methods for using such ligands for receptor localization studies.
    提供了具有以下式子的杂原烷基取代的联苯-4-羧酸芳基酰胺类似物:其中变量如本文所述。这些化合物是配体,可用于体内或体外调节特定受体活性,并在治疗与人类、家畜伴侣动物和牲畜中的病理受体激活相关的疾病方面特别有用。还提供了用于治疗这些疾病的制药组合物和方法,以及用于受体定位研究的这些配体的方法。
  • Inhibitors of Bruton's tyrosine kinase
    申请人:Dewdney Nolan James
    公开号:US20090306041A1
    公开(公告)日:2009-12-10
    This application discloses 5-phenyl-1H-pyridin-2-one and 6-phenyl-2H-pyridazin-3-one derivatives according to generic Formulae I-III: wherein, variables R, X, Y 1 , Y 2 , Y 3 , Y 4 , n and m are defined as described herein, which inhibit Btk. The compounds disclosed herein are useful to modulate the activity of Btk and treat diseases associated with excessive Btk activity. The compounds are further useful to treat inflammatory and auto immune diseases associated with aberrant B-cell proliferation such as rheumatoid arthritis. Also disclosed are compositions containing compounds of Formulae I-III and at least one carrier, diluent or excipient.
    本申请披露了根据通用式I-III公式的5-苯基-1H-吡啶-2-酮和6-苯基-2H-吡嗪-3-酮衍生物:其中,变量R、X、Y1、Y2、Y3、Y4、n和m的定义如本文所述,它们抑制Btk。本文所披露的化合物有助于调节Btk的活性并治疗与过度Btk活性相关的疾病。此外,这些化合物还有助于治疗与异常B细胞增殖相关的炎症和自身免疫性疾病,如类风湿性关节炎。还披露了含有公式I-III化合物和至少一种载体、稀释剂或赋形剂的组合物。
  • Takamatsu, Masanori; Sekiya, Minoru, Chemical and pharmaceutical bulletin, 1980, vol. 28, # 10, p. 3098 - 3105
    作者:Takamatsu, Masanori、Sekiya, Minoru
    DOI:——
    日期:——
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