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N-[2-(4-methylphenoxy)ethyl]acetamide

中文名称
——
中文别名
——
英文名称
N-[2-(4-methylphenoxy)ethyl]acetamide
英文别名
——
N-[2-(4-methylphenoxy)ethyl]acetamide化学式
CAS
——
化学式
C11H15NO2
mdl
MFCD00819341
分子量
193.246
InChiKey
ZAPFOLMPTJGPGD-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):
    1.6
  • 重原子数:
    14
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.363
  • 拓扑面积:
    38.3
  • 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

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文献信息

  • METHODS FOR TREATING ARENAVIRIDAE AND CORONAVIRIDAE VIRUS INFECTIONS
    申请人:Gilead Sciences, Inc.
    公开号:US20170071964A1
    公开(公告)日:2017-03-16
    Provided are methods for treating Arenaviridae and Coronaviridae virus infections by administering nucleosides and prodrugs thereof, of Formula I: wherein the 1′ position of the nucleoside sugar is substituted. The compounds, compositions, and methods provided are particularly useful for the treatment of Lassa virus and Junin virus infections.
    提供了通过给予核苷和其前药治疗Arenaviridae和Coronaviridae病毒感染的方法,其化学式为I: 其中核苷糖的1'位置被取代。所提供的化合物、组合物和方法特别适用于治疗拉沙病毒和胡宁病毒感染。
  • ANTI-INFLAMMATORY PHOSPHONATE COMPOUNDS
    申请人:Cannizzaro Carina
    公开号:US20090247488A1
    公开(公告)日:2009-10-01
    The invention is related to phosphorus substituted anti-inflammatory compounds, compositions containing such compounds, and therapeutic methods that include the administration of such compounds, as well as to processes and intermediates useful for preparing such compounds.
    本发明涉及磷取代的抗炎化合物、含有这种化合物的组合物、包括给药这种化合物的治疗方法,以及用于制备这种化合物的有用过程和中间体。
  • METHODS FOR TREATING HEPATITIS C
    申请人:Karp Gary Mitchell
    公开号:US20120009142A1
    公开(公告)日:2012-01-12
    In accordance with the present invention, compounds that inhibit viral replication, preferably Hepatitis C Virus (HCV) replication, have been identified, and methods for their use provided. In one aspect of the invention, compounds useful in the treatment or prevention of a viral infection are provided. In another aspect of the invention, compounds useful in the treatment or prevention of HCV infection are provided.
    根据本发明,已经鉴定出抑制病毒复制的化合物,优选地是抑制丙型肝炎病毒(HCV)复制的化合物,并提供了使用这些化合物的方法。在本发明的一个方面,提供了用于治疗或预防病毒感染的化合物。在本发明的另一个方面,提供了用于治疗或预防HCV感染的化合物。
  • NOVEL PYRIDINONE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2-RECEPTORS
    申请人:Janssen Pharmaceuticals, Inc.
    公开号:US20130109652A1
    公开(公告)日:2013-05-02
    The present invention relates to novel compounds, in particular novel pyridinone derivatives according to Formula (I) wherein all radicals are defined in the application. The compounds according to the invention are positive allosteric modulators of metabotropic receptors—subtype 2 (“mGluR2”) which are useful for the treatment or prevention of neurological and psychiatric disorders associated with glutamate dysfunction and diseases in which the mGluR2 subtype of metabotropic receptors is involved. In particular, such diseases are central nervous system disorders selected from the group of anxiety, schizophrenia, migraine, depression, and epilepsy. The invention is also directed to pharmaceutical compositions and processes to prepare such compounds and compositions, as well as to the use of such compounds for the prevention and treatment of such diseases in which mGluR2 is involved.
    本发明涉及新型化合物,特别是新型吡啶酮衍生物,公式(I)如下:其中所有基团在申请中定义。本发明的化合物是代谢型受体亚型2(“mGluR2”)的正向变构调节剂,可用于治疗或预防与谷氨酸功能障碍有关的神经和精神障碍以及涉及代谢型受体亚型mGluR2的疾病。特别地,这些疾病是来自焦虑、精神分裂症、偏头痛、抑郁症和癫痫的中枢神经系统疾病。本发明还涉及制备这种化合物和组合物的制药组合物和过程,以及使用这种化合物预防和治疗涉及mGluR2的这些疾病。
  • 1-(4-substituted phenyl)-1H-imidazoles as cardiovascular agents
    申请人:SCHERING AKTIENGESELLSCHAFT
    公开号:EP0306440A2
    公开(公告)日:1989-03-08
    Novel 1-(4-substituted phenyl)-1H-imidazoles and their use as antiarrhythmic, anti-hypertensive and anti-ischemic agents is described. Pharmaceutical formulations containing such compounds are also discussed.
    介绍了新型 1-(4-取代苯基)-1H-咪唑类化合物及其作为抗心律失常、抗高血压和抗缺血药物的用途。还讨论了含有此类化合物的药物制剂。
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