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6-(1,2,3,4,10,14b-hexahydrodibenzo[c,f]pyrazino[1,2-a]azepin-2-yl)hexanoic acid

中文名称
——
中文别名
——
英文名称
6-(1,2,3,4,10,14b-hexahydrodibenzo[c,f]pyrazino[1,2-a]azepin-2-yl)hexanoic acid
英文别名
6-(1,2,3,4,10,14b-hexahydrodibenzo[c,f]pyrazino[1,2-a]azepin-2-yl)caproic acid;6-(2,5-Diazatetracyclo[13.4.0.02,7.08,13]nonadeca-1(19),8,10,12,15,17-hexaen-5-yl)hexanoic acid
6-(1,2,3,4,10,14b-hexahydrodibenzo[c,f]pyrazino[1,2-a]azepin-2-yl)hexanoic acid化学式
CAS
——
化学式
C23H28N2O2
mdl
——
分子量
364.488
InChiKey
VUKQGADZCYFWQK-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):
    1.7
  • 重原子数:
    27
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    43.8
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • Novel tetracyclic compounds having anti-allergic and anti-asthmatic activities, their preparation and use
    申请人:Sankyo Company Limited
    公开号:EP0421823A2
    公开(公告)日:1991-04-10
    Compounds of formula (I): [in which; Q is nitrogen or =CH-; R1 and R2 are hydrogen, alkyl, alkoxy, hydroxy, trifluoromethyl or halogen; and R3 is various specific substituted alkyl groups] and pharmaceutically acceptable salts thereof have valuable anti-allergic and anti-asthmatic activities. They may be prepared by reacting a corresponding compound where R3 is replaced by a hydrogen atom with a compound to introduce the group R3.
    式(I)化合物: [其中,Q 为氮或 =CH-;R1 和 R2 为氢、烷基、烷氧基、羟基、三氟甲基或卤素;R3 为各种特定的取代烷基]及其药学上可接受的盐类具有重要的抗过敏和抗哮喘活性。它们可以通过将 R3 被氢原子取代的相应化合物与引入基团 R3 的化合物反应来制备。
  • A polycyclic compound, method for preparing the same, and pharmaceutical composition comprising the same
    申请人:HOKURIKU PHARMACEUTICAL CO., LTD.
    公开号:EP0447857A1
    公开(公告)日:1991-09-25
    Novel polycyclic compounds represented by the following formula: A - (CH₂)n - COOR¹, wherein R¹ represents a hydrogen atom or a lower alkyl group; n represents an integer of from 0 to 5; and A is a group represented by the following formula: wherein X represents a hydrogen atom or a halogen atom; and Y represents a methylene group, an oxygen atom, or a sulfur atom, or A is a group represented by the following formula: and pharmacologically acceptable salts thereof are disclosed. Also disclosed are a method for preparing the same, a pharmaceutical composition comprising the same, an antiallergic agent and an agent for bronchial asthma comprising the same, and a method for treatment of an allergic disease or bronchial asthma comprising the step of administering the same.
    由下式表示的新型多环化合物:A - (CH₂)n - COOR¹,其中 R¹ 代表氢原子或低级烷基;n 代表 0 至 5 的整数;以及 A 是下式所代表的基团: 其中 X 代表氢原子或卤原子;Y 代表亚甲基、氧原子或硫原子,或者 A 是下式所代表的基团: 及其药理上可接受的盐类。还公开了制备上述物质的方法、包含上述物质的药物组合物、包含上述物质的抗过敏制剂和支气管哮喘制剂,以及包含给药步骤的治疗过敏性疾病或支气管哮喘的方法。
  • Methods of treating a sleep disorder
    申请人:Edgar M. Dale
    公开号:US20060063754A1
    公开(公告)日:2006-03-23
    The invention relates to methods of modulating sleep.
    本发明涉及调节睡眠的方法。
  • US5344828A
    申请人:——
    公开号:US5344828A
    公开(公告)日:1994-09-06
  • US5362725A
    申请人:——
    公开号:US5362725A
    公开(公告)日:1994-11-08
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