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1-(2-羟基乙基)哌啶-4-羧酸 | 16665-18-2

中文名称
1-(2-羟基乙基)哌啶-4-羧酸
中文别名
——
英文名称
N-(2-Hydroxyethyl)-piperidin-4-carbonsaeure
英文别名
1-(2-hydroxyethyl)piperidine-4-carboxylic acid;1-(2-hydroxyethyl)piperidin-1-ium-4-carboxylate
1-(2-羟基乙基)哌啶-4-羧酸化学式
CAS
16665-18-2
化学式
C8H15NO3
mdl
MFCD04107783
分子量
173.212
InChiKey
LZJPEZQINGNPQY-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

物化性质

  • 熔点:
    185 °C
  • 沸点:
    345.3±32.0 °C(Predicted)
  • 密度:
    1.195±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -2.7
  • 重原子数:
    12
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.875
  • 拓扑面积:
    60.8
  • 氢给体数:
    2
  • 氢受体数:
    4

安全信息

  • 危险等级:
    IRRITANT
  • 海关编码:
    2933399090
  • 危险类别:
    IRRITANT

文献信息

  • Diarylamine-Containing Compounds and Compositions, and their use as Modulators of C-Kit Receptors
    申请人:Molteni Valentina
    公开号:US20070149538A1
    公开(公告)日:2007-06-28
    Described herein are compounds that include a diarylamine structural feature. Also described herein are methods for making such compounds, methods for using such compounds to modulate the activity of c-kit receptors, and pharmaceutical compositions and medicaments comprising such compounds. Also described herein are methods of using such compounds, pharmaceutical compositions and medicaments to treat and/or prevent and/or inhibit and/or ameliorate the pathology and/or symptomology diseases or conditions associated with the activity of c-kit receptors.
    本文描述了包含二芳胺结构特征的化合物。还描述了制备这种化合物的方法,使用这种化合物调节c-kit受体活性的方法,以及包含这种化合物的药物组合物和药物。本文还描述了使用这种化合物、药物组合物和药物治疗和/或预防和/或抑制和/或改善与c-kit受体活性相关的病理学和/或症状学疾病或状况的方法。
  • Tyrosine kinase inhibitors
    申请人:Fraley Mark E.
    公开号:US20080274107A1
    公开(公告)日:2008-11-06
    The present invention relates to compounds which inhibit, regulate and/or modulate tyrosine kinase signal transduction, compositions which contain these compounds, and methods of using them to treat tyrosine kinase-dependent diseases and conditions, such as angiogenesis, cancer, tumor growth, atherosclerosis, age related macular degeneration, diabetic retinopathy, inflammatory diseases, and the like in mammals.
    本发明涉及抑制、调节和/或调节酪氨酸激酶信号传导的化合物,含有这些化合物的组合物,以及使用它们治疗哺乳动物中的酪氨酸激酶依赖性疾病和病状的方法,如血管生成、癌症、肿瘤生长、动脉硬化、年龄相关性黄斑变性、糖尿病视网膜病变、炎症性疾病等。
  • PROTEASE INHIBITORS
    申请人:Orion Corporation
    公开号:US20140200225A1
    公开(公告)日:2014-07-17
    A compound of formula (I) wherein R 1 to R 15 , P 1 , P 2 , A, B and Q are as defined in the claims and pharmaceutically acceptable salts and esters thereof, are disclosed. The compounds of formula (I) possess utility as matriptase inhibitors and are useful in the treatment of matriptase dependent conditions, particularly cancer.
    公式(I)的化合物,其中R1到R15,P1,P2,A,B和Q如权利要求所定义,并且其药物可接受的盐和酯被揭示。公式(I)的化合物具有作为matriptase抑制剂的效用,并且在治疗matriptase依赖性疾病,特别是癌症方面有用。
  • PYRIDINE SUBSTITUTED FURAN DERIVATIVES AS RAF KINASE INHIBITORS
    申请人:SMITHKLINE BEECHAM PLC
    公开号:EP1423383A1
    公开(公告)日:2004-06-02
  • US7186723B2
    申请人:——
    公开号:US7186723B2
    公开(公告)日:2007-03-06
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