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2-Hydroxymethyl-2-nonyloxirane | 135214-51-6

中文名称
——
中文别名
——
英文名称
2-Hydroxymethyl-2-nonyloxirane
英文别名
2-nonyloxiranemethanol;(2-Nonyloxiran-2-yl)methanol
2-Hydroxymethyl-2-nonyloxirane化学式
CAS
135214-51-6
化学式
C12H24O2
mdl
——
分子量
200.321
InChiKey
MTZGPCUBNFEIST-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):
    3.6
  • 重原子数:
    14
  • 可旋转键数:
    9
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    32.8
  • 氢给体数:
    1
  • 氢受体数:
    2

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

  • 作为反应物:
    描述:
    2-Hydroxymethyl-2-nonyloxirane乙酸乙烯酯 作用下, 以 氯仿 为溶剂, 反应 2.0h, 以36%的产率得到(2S)-2-hydroxymethyl-2-nonyloxirane
    参考文献:
    名称:
    Enzymic resolution of 2-substituted oxiranemethanols, a class of synthetically useful building blocks, bearing a chiral quaternary center
    摘要:
    DOI:
    10.1021/jo00018a057
  • 作为产物:
    描述:
    1-溴壬烷 在 vanadium acetylacetonate 叔丁基过氧化氢二异丁基氢化铝 作用下, 以 四氢呋喃 为溶剂, 反应 363.0h, 生成 2-Hydroxymethyl-2-nonyloxirane
    参考文献:
    名称:
    Enzymic resolution of 2-substituted oxiranemethanols, a class of synthetically useful building blocks, bearing a chiral quaternary center
    摘要:
    DOI:
    10.1021/jo00018a057
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文献信息

  • Floerke, Holger; Schaumann, Ernst, Liebigs Annalen, 1996, # 1, p. 147 - 152
    作者:Floerke, Holger、Schaumann, Ernst
    DOI:——
    日期:——
  • TREATMENT OF VIRAL INFECTIONS BY MODULATION OF HOST CELL METABOLIC PATHWAYS
    申请人:THE TRUSTEES OF PRINCETON UNIVERSITY
    公开号:EP2166843A2
    公开(公告)日:2010-03-31
  • ANTI-VIRAL COMBINATION THERAPY
    申请人:THE TRUSTEES OF PRINCETON UNIVERSITY
    公开号:EP2725902A2
    公开(公告)日:2014-05-07
  • [EN] TREATMENT OF VIRAL INFECTIONS BY MODULATION OF HOST CELL METABOLIC PATHWAYS<br/>[FR] TRAITEMENT D'INFECTIONS VIRALES PAR MODULATION DE VOIES MÉTABOLIQUES DE CELLULES HÔTES
    申请人:UNIV PRINCETON
    公开号:WO2009023059A2
    公开(公告)日:2009-02-19
    Alterations of certain metabolite concentrations and fluxes that occur in response to viral infection are described. Host cell enzymes in the involved metabolic pathways are selected as targets for intervention; i.e., to restore metabolic flux to disadvantage viral replication, or to further derange metabolic flux resulting in 'suicide' of viral-infected cells (but not uninfected cells) in order to limit viral propagation. While any of the enzymes in the relevant metabolic pathway can be selected, pivotal enzymes at key control points in these metabolic pathways are preferred as candidate antiviral drug targets. Inhibitors of these enzymes are used to reverse, or redirect, the effects of the viral infection. Drug candidates are tested for antiviral activity using screening assays in vitro and host cells, as well as in animal models. Animal models are then used to test efficacy of candidate compounds in preventing and treating viral infections. The antiviral activity of enzyme inhibitors is demonstrated.
  • [EN] ANTI-VIRAL COMBINATION THERAPY<br/>[FR] POLYTHÉRAPIE ANTIVIRALE
    申请人:UNIV PRINCETON
    公开号:WO2012139028A2
    公开(公告)日:2012-10-11
    The present invention provides methods and compounds for treating viral infections using combinations modulators of an HCV-associated component and modulators of host cell enzymes. The present invention also provides methods and compounds for treating viral infections using combinations of modulators of host cell enzymes and other agents that work, at least in part by modulating host factors.
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