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1,5-dimethoxy-pent-2t-ene | 28000-00-2

中文名称
——
中文别名
——
英文名称
1,5-dimethoxy-pent-2t-ene
英文别名
1,5-Dimethoxy-pent-2t-en;(E)-1,5-dimethoxypent-2-ene
1,5-dimethoxy-pent-2<i>t</i>-ene化学式
CAS
28000-00-2
化学式
C7H14O2
mdl
——
分子量
130.187
InChiKey
YGGBDWAMYZMGFP-ONEGZZNKSA-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):
    0.7
  • 重原子数:
    9
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

点击查看最新优质反应信息

文献信息

  • MACROCYCLIC, PYRIDAZINONE-CONTAINING HEPATITIS C SERINE PROTEASE INHIBITORS
    申请人:Moore Joel D.
    公开号:US20090123425A1
    公开(公告)日:2009-05-14
    The present invention relates to compounds of Formula I, II, or III, or pharmaceutically acceptable salts, esters, or prodrugs thereof: which inhibit serine protease activity, particularly the activity of hepatitis C virus (HCV) NS3-NS4A protease. Consequently, the compounds of the present invention interfere with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from HCV infection. The invention also relates to methods of treating an HCV infection in a subject by administering a pharmaceutical composition comprising a compound of the present invention.
    本发明涉及公式I、II或III的化合物,或其药用可接受的盐、酯或前药: 其抑制丝氨酸蛋白酶活性,尤其是丙型肝炎病毒(HCV)NS3-NS4A蛋白酶的活性。因此,本发明的化合物干扰丙型肝炎病毒的生命周期,并且也用作抗病毒剂。本发明进一步涉及包含用于给予受HCV感染的主体的前述化合物的药物组合物。本发明还涉及通过给予包含本发明化合物的药物组合物来治疗主体中的HCV感染的方法。
  • INDOLE COMPOUND AND USE THEREOF
    申请人:ONO PHARMACEUTICAL CO., LTD.
    公开号:EP1852420A1
    公开(公告)日:2007-11-07
    The present invention relates to a compound represented by the formula (I), wherein all symbols are as defined in the description, a salt thereof a solvate thereof, or a prodrug thereof, which has a leukotriene receptor antagonistic activity which is expected to be more effective than those of the leukotriene receptor antagonists currently used in clinical trials. Therefore, it is useful as an agent for the prevention and/or treatment of a leukotriene-mediated disease such as a respiratory diseases such as bronchial asthma, chronic obstructive pulmonary disease, pulmonary emphysema, chronic bronchitis, pneumonia (e.g. interstitial pneumonia etc.), severe acute respiratory syndrome (SARS), acute respiratory distress syndrome (ARDS), allergic rhinitis, sinusitis (e.g. acute sinusitis, chronic sinusitis, etc.), or the like, or as an expectorant or an antitussive.
    本发明涉及一种由式 (I) 代表的化合物、 本发明涉及一种由式(I)表示的化合物,其中所有符号如描述中所定义,它的盐,它的溶解物,或它的原药,它具有白三烯受体拮抗活性,预计比目前用于临床试验的白三烯受体拮抗剂更有效。因此,它可用作预防和/或治疗白三烯介导的疾病的药物,如支气管哮喘、慢性阻塞性肺病、肺气肿、慢性支气管炎、肺炎(如间质性肺炎等)等呼吸系统疾病。如间质性肺炎等)、严重急性呼吸系统综合征(SARS)、急性呼吸窘迫综合征(ARDS)、过敏性鼻炎、鼻窦炎(如急性鼻窦炎、慢性鼻窦炎等)等,或作为祛痰剂或抗鼻炎药。
  • Indole compounds for treating respiratory disorders
    申请人:ONO PHARMACEUTICAL CO., LTD.
    公开号:EP1852420B1
    公开(公告)日:2012-10-17
  • US8383583B2
    申请人:——
    公开号:US8383583B2
    公开(公告)日:2013-02-26
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