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ethyl 1-(2-aminoethyl)piperidine-4-carboxylate | 752181-51-4

中文名称
——
中文别名
——
英文名称
ethyl 1-(2-aminoethyl)piperidine-4-carboxylate
英文别名
——
ethyl 1-(2-aminoethyl)piperidine-4-carboxylate化学式
CAS
752181-51-4
化学式
C10H20N2O2
mdl
——
分子量
200.281
InChiKey
FDWYQACDSWSSAS-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
  • 重原子数:
    14
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    55.6
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    ethyl 1-(2-aminoethyl)piperidine-4-carboxylate 在 Raney nickel 氢气硼酸溶剂黄1461,8-二氮杂双环[5.4.0]十一碳-7-烯 、 lithium hydroxide 作用下, 以 四氢呋喃乙醇N,N-二甲基乙酰胺二甲基亚砜 为溶剂, 18.0~100.0 ℃ 、101.33 kPa 条件下, 反应 42.5h, 生成 1-[2-(8-benzylamino-7-methyl-2,4-dioxo-3,4-dihydrobenzo[g]pteridin-10(2H)-yl)ethyl]piperidine-4-carboxylic acid acetate
    参考文献:
    名称:
    [EN] FLAVIN DERIVATIVES
    [FR] DÉRIVÉS DES FLAVINES
    摘要:
    本发明涉及新型黄素衍生物和其他黄素衍生物,它们的用途和用作核糖开关配体和/或抗感染剂的组合物。该发明还提供了制备新型黄素衍生物的方法。
    公开号:
    WO2011008247A1
  • 作为产物:
    参考文献:
    名称:
    HETEROCYCLIC DERIVATIVES AS JANUS KINASE INHIBITORS
    摘要:
    The present invention relates to a compounds of general formula (I) inhibiting the JAK family of non-receptor tyrosine protein kinases (JAK1, JAK2, JAK3, and TYK2); methods of preparing such compounds, pharmaceutical compositions containing them and therapeutic use thereof. The compounds of the invention may be useful in the treatment of diseases or conditions associated with a dysregulation of the JAK family non-receptor kinases; in particular for the treatment of various inflammatory disease including asthma, COPD and other respiratory diseases.
    公开号:
    WO2024052513A1
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文献信息

  • Substituted-Quinoxaline-Type Piperidine Compounds and the Uses Thereof
    申请人:FUCHINO Kouki
    公开号:US20100216726A1
    公开(公告)日:2010-08-26
    The invention relates to Substituted-Quinoxaline-Type Piperidine Compounds, compositions comprising an effective amount of a Substituted-Quinoxaline-Type Piperidine Compound and methods to treat or prevent a condition, such as pain, comprising administering to an animal in need thereof an effective amount of a Substituted-Quinoxaline-Type Piperidine Compound.
    本发明涉及取代喹喔啉型哌啶化合物、包含有效量取代喹喔啉型哌啶化合物的组合物以及治疗或预防某种疾病(如疼痛)的方法,包括向需要治疗的动物施用有效量取代喹喔啉型哌啶化合物。
  • FLAVIN DERIVATIVES
    申请人:Blount Kenneth F.
    公开号:US20120295903A1
    公开(公告)日:2012-11-22
    The present invention relates novel flavin derivatives and other flavin derivatives, their use and compositions for use as riboswitch ligands and/or anti-infectives. The invention also provides method of making novel flavin derivatives.
    本发明涉及新型黄素衍生物和其他黄素衍生物,它们的用途和组合物用作核糖开关配体和/或抗感染剂。本发明还提供制备新型黄素衍生物的方法。
  • SUBSTITUTED-QUINOXALINE-TYPE PIPERIDINE COMPOUNDS AND THE USES THEREOF
    申请人:Purdue Pharma L.P.
    公开号:US20150141643A1
    公开(公告)日:2015-05-21
    The invention relates to Substituted-Quinoxaline-Type Piperidine Compounds, compositions comprising an effective amount of a Substituted-Quinoxaline-Type Piperidine Compound and methods to treat or prevent a condition, such as pain, comprising administering to an animal in need thereof an effective amount of a Substituted-Quinoxaline-Type Piperidine Compound.
    该发明涉及取代喹喔啉型哌啶化合物,包括一种有效量的取代喹喔啉型哌啶化合物的组合物以及治疗或预防疾病的方法,例如疼痛,通过向需要治疗的动物施用一种有效量的取代喹喔啉型哌啶化合物。
  • [EN] PROTEIN STABILIZING COMPOUNDS CONTAINING USP28 AND/OR USP25 TARGETING LIGANDS<br/>[FR] COMPOSÉS DE STABILISATION DE PROTÉINES CONTENANT DES LIGANDS CIBLANT USP28 ET/OU USP25
    申请人:STABLIX INC
    公开号:WO2023122298A1
    公开(公告)日:2023-06-29
    This invention provides protein stabilizing compounds that have a USP28 Targeting Ligand or USP25 Targeting Ligand, a Protein Targeting Ligand, and optionally a Linker, wherein the Target Protein is ubiquitinated. The protein stabilizing compounds of the present invention can be used to deubiquitinate the Ubiquitinated Target Protein and thus increase the concentration and/or function of the Target Protein.
    本发明提供的蛋白质稳定化合物具有 USP28 靶向配体或 USP25 靶向配体、蛋白质靶向配体和可选的连接体,其中靶蛋白被泛素化。本发明的蛋白质稳定化合物可用于泛素化目标蛋白的去泛素化,从而提高目标蛋白的浓度和/或功能。
  • Substituted-quinoxaline-type-piperidine compounds and the uses thereof
    申请人:Purdue Pharma LP
    公开号:EP2433935A1
    公开(公告)日:2012-03-28
    The invention relates to Substituted-Quinoxaline-Type Piperidine Compounds of Formula (I) and Formula (II), compositions comprising an effective amount of a Substituted-Quinoxaline-Type Piperidine Compound and methods to treat or prevent a condition, such as pain, comprising administering to an animal in need thereof an effective amount of a Substituted-Quinoxaline-Type Piperidine Compound.
    本发明涉及式(I)和式(II)的取代喹喔啉型哌啶化合物、包含有效量的取代喹喔啉型哌啶化合物的组合物,以及治疗或预防疼痛等疾病的方法,包括向有需要的动物施用有效量的取代喹喔啉型哌啶化合物。
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