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1-(4-Ethylphenyl)piperidine-4-carboxylic acid | 1241894-78-9

中文名称
——
中文别名
——
英文名称
1-(4-Ethylphenyl)piperidine-4-carboxylic acid
英文别名
——
1-(4-Ethylphenyl)piperidine-4-carboxylic acid化学式
CAS
1241894-78-9
化学式
C14H19NO2
mdl
——
分子量
233.31
InChiKey
RIVCPNNWLKPMQZ-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):
    2.9
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    40.5
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • [EN] AMINE COMPOUNDS<br/>[FR] DERIVES D'INDOLE SERVANT D'ANTAGONISTE DE SOMATOSTATINE
    申请人:TAKEDA CHEMICAL INDUSTRIES LTD
    公开号:WO2004046107A1
    公开(公告)日:2004-06-03
    The present invention provide a compound of the formula (I) wherein ring A represents an aromatic ring optionally having substituents; B, Y and Ya are the same or different and each represents a bond, etc.; R1 and R2 are the same or different and each represents a hydrogen atom, etc.; R3 represents a hydrogen atom, etc.; R4 and R5 are the same or different and each represents a hydrogen, etc.; R6 represents an indolyl group optionally having substituents; and Z and Za are the same or different and each represents a hydrogen atom, etc.; or a salt thereof or a prodrug thereof, having a somatostatin receptor binding inhibition activity and is useful for preventing and/or treating diseases associated with somatostatin.
    本发明提供了一种公式(I)的化合物,其中环A代表一个具有可选取代基的芳香环;B、Y和Ya相同或不同,分别代表一个键等;R1和R2相同或不同,每个代表一个氢原子等;R3代表一个氢原子等;R4和R5相同或不同,每个代表一个氢等;R6代表一个可选有取代基的吲哚基团;Z和Za相同或不同,每个代表一个氢原子等;或其盐或前药,具有生长抑素受体结合抑制活性,并且用于预防或治疗与生长抑素相关的疾病。
  • [EN] DIHYDROPYRAZOLOPYRIDINE COMPOUNDS<br/>[FR] COMPOSES DE DIHYDROPYRAZOLOPYRIDINE
    申请人:MITSUBISHI PHARMA CORP
    公开号:WO2004014910A1
    公开(公告)日:2004-02-19
    The present invention provides dihydropyrazolopyridine compounds represented by the formula (I):wherein each symbol is as defined in the specification, optically active forms thereof, and pharmaceutically acceptable salts thereof and hydrates thereof. The compounds of the present invention show a selective and strong inhibitory activity on glycogen synthase kinase-3 beta (GSK-3β), and are useful as medicaments for prevention and/or treatment of diabetes, diabetic complications and neurodegenerative diseases or as immunopotentiators.
    本发明提供了由式(I)表示的二氢吡唑吡啶化合物,其中每个符号如规范中定义,其光学活性形式,以及其药学上可接受的盐和水合物。本发明的化合物显示出对糖原合成酶激酶-3β(GSK-3β)的选择性和强烈的抑制活性,并可用作预防和/或治疗糖尿病、糖尿病并发症和神经退行性疾病或免疫增强剂的药物。
  • DIHYDROPYRAZOLOPYRIDINE COMPOUNDS
    申请人:Mitsubishi Pharma Corporation
    公开号:EP1537106A1
    公开(公告)日:2005-06-08
  • INDOLE DERIVATIVES AS SOMATOSTATIN AGONISTS OR ANTAGONISTS
    申请人:Takeda Pharmaceutical Company Limited
    公开号:EP1562898A1
    公开(公告)日:2005-08-17
  • Anti-Infective Compounds
    申请人:INSTITUT PASTEUR KOREA
    公开号:US20160185774A1
    公开(公告)日:2016-06-30
    The present invention relates to small molecule compounds and their use in the treatment of bacterial infections, in particular Tuberculosis.
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