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3-(1-adamantyl)-1-(aminomethyl)-3,4-dihydro-1H-isochromene-5,6-diol

中文名称
——
中文别名
——
英文名称
3-(1-adamantyl)-1-(aminomethyl)-3,4-dihydro-1H-isochromene-5,6-diol
英文别名
——
3-(1-adamantyl)-1-(aminomethyl)-3,4-dihydro-1H-isochromene-5,6-diol化学式
CAS
——
化学式
C20H27NO3
mdl
——
分子量
329.4
InChiKey
QLJOSZATCBCBDR-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
  • 重原子数:
    24
  • 可旋转键数:
    2
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    75.7
  • 氢给体数:
    3
  • 氢受体数:
    4

文献信息

  • Carbamoyl esters that inhibit cholinesterase and release pharmacologically active agents
    申请人:Verheijen C. Jeroen
    公开号:US20050096387A1
    公开(公告)日:2005-05-05
    Carbamoyl esters inhibit cholinesterase activity and, upon hydrolysis release a pharmacologically active agent. In one embodiment, the carbamoyl ester has the following structure: wherein A is selected from the group consisting of an unsubstituted aryl, a substituted aryl, an unsubstituted heteroaryl and a substituted heteroaryl. The carbamoyl esters are employed in methods to treat an individual. The pharmacologically active agent obtained by hydrolysis of the carbamoyl esters can treat, for example, a nervous system condition, a cholinergic deficiency and conditions or diseases associated with a deficiency in a pharmacologically active agent, such as acetylcholine.
    碳酰基酯抑制胆碱酯酶活性,水解后释放出药理活性成分。在一种实施例中,碳酰基酯具有以下结构:其中A选自无取代芳基、取代芳基、无取代杂环芳基和取代杂环芳基的群组。碳酰基酯用于治疗个体的方法中。通过水解碳酰基酯获得的药理活性成分可以治疗例如神经系统疾病、胆碱能缺乏以及与药理活性成分缺乏相关的疾病或病症,例如乙酰胆碱。
  • DOPAMINE AGONISTS
    申请人:ABBOTT LABORATORIES
    公开号:EP0474767A1
    公开(公告)日:1992-03-18
  • EP0474767A4
    申请人:——
    公开号:EP0474767A4
    公开(公告)日:1992-07-08
  • 3- (1' -ADAMANTYL) - 1 - AMINOMETHYL - 3, 4 - DIHYDRO - 5, 6 - DIHYDROXY - 1H - 2 - BENZOPYRAN FOR USE IN THE TREATMENT OF A DISEASE ASSOCIATED WITH BETA-AMYLOID INDUCED TOXICITY
    申请人:The University Of Manchester
    公开号:EP2844244A1
    公开(公告)日:2015-03-11
  • Carbamoyl Esters That Inhibit Cholinesterase And Release Pharmacologically Active Agents
    申请人:Verheijen C. Jeroen
    公开号:US20070275959A1
    公开(公告)日:2007-11-29
    Carbamoyl esters inhibit cholinesterase activity and, upon hydrolysis release a pharmacologically active agent. In one embodiment, the carbamoyl ester has the following structure: Formula (I) wherein A is selected from the group consisting of an unsubstituted aryl, a substituted aryl, an unsubstituted heteroaryl and a substituted heteroaryl. The carbamoyl esters are employed in methods to treat an individual. The pharmacologically active agent obtained by hydrolysis of the carbamoyl esters can treat, for example, a nervous system condition, a cholinergic deficiency and conditions or diseases associated with a deficiency in a pharmacologically active agent, such as acetylcholine.
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