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2-(4-pyridin-3-ylmethyl-piperazin-1-yl)-ethylamine | 874832-08-3

中文名称
——
中文别名
——
英文名称
2-(4-pyridin-3-ylmethyl-piperazin-1-yl)-ethylamine
英文别名
2-[4-(Pyridin-3-ylmethyl)piperazin-1-yl]ethanamine
2-(4-pyridin-3-ylmethyl-piperazin-1-yl)-ethylamine化学式
CAS
874832-08-3
化学式
C12H20N4
mdl
MFCD06808639
分子量
220.318
InChiKey
VWWVVWYWSHOHFY-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):
    -0.7
  • 重原子数:
    16
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.583
  • 拓扑面积:
    45.4
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • 3-Imidazolyl-Indoles for the Treatment of Proliferative Diseases
    申请人:Boettcher Andreas
    公开号:US20100125064A1
    公开(公告)日:2010-05-20
    The invention relates to 3-heterocyclyl indolyl compounds capable of inhibiting the interaction between p53, or variants thereof, and MDM2 and/or MDM4, or variants thereof, respectively, said compounds having the formula I, wherein R 1 , R 2 , R 3 , R 4 , R A , Y and Y are as defined in the specification. Due to their activity, the compounds are useful in the treatment of various disorders and diseases mediated by the activity of MDM2 and/or MDM4, or variants thereof, such as inflammatory or proliferative diseases or in the protection of cells.
    本发明涉及能够抑制p53或其变体与MDM2和/或MDM4或其变体相互作用的3-杂环基吲哚化合物,其中所述化合物具有式I,其中R1、R2、R3、R4、RA、Y和Y的定义见说明书。由于其活性,这些化合物可用于治疗由MDM2和/或MDM4或其变体介导的各种疾病和疾病,例如炎症性或增殖性疾病或细胞保护。
  • Triterpene amine derivatives
    申请人:DFH THERAPEUTICS
    公开号:US11236122B2
    公开(公告)日:2022-02-01
    The present invention concerns novel pharmaceutically active triterpene amine derivatives, pharmaceutical compositions containing the same, their use as medicaments, and the use of the compounds for the manufacture of specific medicaments. The present invention also concerns a method of treatment involving administration of the triterpene amine compounds. Specifically, the compounds are derivatives of betulinic acid having substitutions at one or more of the C-3, C-28 and C-19 positions as further described herein. The novel compounds are useful as antiretroviral agents. In particular, the novel compounds are useful for the treatment of Human Immunodeficiency Virus-1 (HIV-1).
    本发明涉及新型具有药用活性的三萜胺衍生物、含有三萜胺衍生物的药物组合物、其作为药物的用途,以及使用这些化合物制造特定药物。本发明还涉及一种涉及三萜胺化合物给药的治疗方法。具体来说,这些化合物是白桦脂酸的衍生物,在 C-3、C-28 和 C-19 位上有一个或多个取代位,如本文进一步描述的那样。这些新型化合物可用作抗逆转录病毒药物。特别是,这些新型化合物可用于治疗人类免疫缺陷病毒-1(HIV-1)。
  • 3-IMIDAZOLYL-INDOLES FOR THE TREATMENT OF PROLIFERATIVE DISEASES
    申请人:Novartis AG
    公开号:EP2142535A2
    公开(公告)日:2010-01-13
  • TRITERPENE AMINE DERIVATIVES
    申请人:DFH THERAPEUTICS
    公开号:US20210253627A1
    公开(公告)日:2021-08-19
    The present invention concerns novel pharmaceutically active triterpene amine derivatives, pharmaceutical compositions containing the same, their use as medicaments, and the use of the compounds for the manufacture of specific medicaments. The present invention also concerns a method of treatment involving administration of the triterpene amine compounds. Specifically, the compounds are derivatives of betulinic acid having substitutions at one or more of the C-3, C-28 and C-19 positions as further described herein. The novel compounds are useful as antiretroviral agents. In particular, the novel compounds are useful for the treatment of Human Immunodeficiency Virus-1 (HIV-1).
  • US8053457B2
    申请人:——
    公开号:US8053457B2
    公开(公告)日:2011-11-08
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