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1-环丙基-4-哌啶甲腈 | 713147-47-8

中文名称
1-环丙基-4-哌啶甲腈
中文别名
——
英文名称
1-cyclopropyl piperidine-4-carbonitrile
英文别名
1-Cyclopropylpiperidine-4-carbonitrile
1-环丙基-4-哌啶甲腈化学式
CAS
713147-47-8
化学式
C9H14N2
mdl
——
分子量
150.224
InChiKey
UCYYYCCUIQMDFT-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
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    27
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:7dceb64ba07fee3996fd8ff471a5dc4b
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 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

  • Substituted homopiperidine, piperidine or pyrrolidine derivatives
    申请人:Sorensen Lindy Jan
    公开号:US20050107434A1
    公开(公告)日:2005-05-19
    A novel class of substituted homopiperidine, piperidine and pyrrolidine derivatives, methods for their preparation, pharmaceutical compositions comprising them and use thereof in the treatment of disorders related to the histamine H3 receptor. More particularly, the compounds possess histamine H3 receptor antagonistic activity and are thus useful in the treatment of disorders in which a histamine H3 receptor blockade is beneficial.
    一种新型的取代的同环丙啶、哌啶和吡咯啶衍生物类别,其制备方法,包含它们的药物组合物以及在治疗与组胺H3受体相关的疾病中的应用。更具体地说,这些化合物具有组胺H3受体拮抗活性,因此在组胺H3受体阻滞有益的疾病治疗中是有用的。
  • HETEROARYL-SUBSTITUTED PIPERIDINES
    申请人:Heimbach Dirk
    公开号:US20090306139A1
    公开(公告)日:2009-12-10
    The invention relates to novel heteroaryl-substituted piperidines, to processes for their preparation, to their use for the treatment and/or prophylaxis of diseases and to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular of cardiovascular diseases and tumour diseases.
    这项发明涉及新颖的杂环取代哌啶,涉及它们的制备过程,涉及它们用于治疗和/或预防疾病以及用于制备治疗和/或预防疾病的药物,特别是心血管疾病和肿瘤疾病。
  • Substituted Homopiperidine, Piperidine or Pyrrolidine Derivatives
    申请人:Sorensen Lindy Jan
    公开号:US20080113995A1
    公开(公告)日:2008-05-15
    A novel class of substituted homopiperidine, piperidine and pyrrolidine derivatives, methods for their preparation, pharmaceutical compositions comprising them and use thereof in the treatment of disorders related to the histamine H3 receptor. More particularly, the compounds possess histamine H3 receptor antagonistic activity and are thus useful in the treatment of disorders in which a histamine H3 receptor blockade is beneficial.
    一种新型的取代的同源吡啶,吡啶和吡咯烷衍生物,其制备方法,包含它们的药物组合物以及在治疗与组胺H3受体相关的疾病中的使用。更具体地说,这些化合物具有组胺H3受体拮抗活性,因此在需要组胺H3受体阻滞有益的疾病治疗中有用。
  • Heteroaryl-substituted piperidines
    申请人:Bayer Pharma Aktiengesellschaft
    公开号:US08119663B2
    公开(公告)日:2012-02-21
    The invention relates to novel heteroaryl-substituted piperidines, to processes for their preparation, to their use for the treatment and/or prophylaxis of diseases and to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular of cardiovascular diseases and tumor diseases.
    本发明涉及新型杂环芳基取代哌啶,其制备过程,以及它们用于治疗和/或预防疾病的用途,以及用于制备治疗和/或预防疾病的药物,特别是心血管疾病和肿瘤疾病。
  • Heteroaryl compounds as 5-HT4 receptor ligands
    申请人:Nirogi Ramakrishna
    公开号:US09079894B2
    公开(公告)日:2015-07-14
    The present invention relates to novel compounds of formula (I), and their pharmaceutically acceptable salts and compositions containing them. The present invention also relates to a process for the preparation of above said novel compounds, and their pharmaceutically acceptable salts. The compounds of formula (I) are useful in the treatment of various disorders that are related to 5-HT4 receptors.
    本发明涉及公式(I)的新化合物,以及它们的药学上可接受的盐和含有它们的组合物。本发明还涉及一种制备上述新化合物及其药学上可接受的盐的方法。公式(I)的化合物在治疗与5-HT4受体有关的各种疾病方面是有用的。
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