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4-{4-[3-(10,11-dihydrodibenzo[b,f]azepin-5-yl)propyl]piperazin-1-yl}butyronitrile | 908486-67-9

中文名称
——
中文别名
——
英文名称
4-{4-[3-(10,11-dihydrodibenzo[b,f]azepin-5-yl)propyl]piperazin-1-yl}butyronitrile
英文别名
N-[3-(10,11-dihydro-dibenzo[b,f]azepin-5-yl)-propyl]-N'-(3-cyanopropyl)-piperazine;N-[3-(10,11-dihydro-dibenzo[b,f]azepine-5-yl)-propyl]-N'-(3-cyanopropyl)-piperazine;4-[4-[3-(5,6-dihydrobenzo[b][1]benzazepin-11-yl)propyl]piperazin-1-yl]butanenitrile
4-{4-[3-(10,11-dihydrodibenzo[b,f]azepin-5-yl)propyl]piperazin-1-yl}butyronitrile化学式
CAS
908486-67-9
化学式
C25H32N4
mdl
——
分子量
388.556
InChiKey
UJOGZXIBGOZBPB-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):
    5.2
  • 重原子数:
    29
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    33.5
  • 氢给体数:
    0
  • 氢受体数:
    4

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

  • 作为反应物:
    描述:
    4-{4-[3-(10,11-dihydrodibenzo[b,f]azepin-5-yl)propyl]piperazin-1-yl}butyronitrile 在 lithium aluminium tetrahydride 作用下, 以 乙醚苯酚 为溶剂, 反应 18.5h, 生成 N-[4-[4-[3-(5,6-dihydrobenzo[b][1]benzazepin-11-yl)propyl]piperazin-1-yl]butyl]acridin-9-amine
    参考文献:
    名称:
    A Chimeric Ligand Approach Leading to Potent Antiprion Active Acridine Derivatives:  Design, Synthesis, and Biological Investigations
    摘要:
    Human transmissible neurodegenerations including Creutzfeldt-Jakob disease are unique, since they are caused by prions, an infectious agent that replicates without nucleic acids but instead by inducing conversion of a host-resident normal prion protein to a misfolded conformational isoform. For pharmacotherapy of these unusual diseases, tricyclic heterocyclic compounds such as quinacrine have been considered, but with ambiguous success in vivo, so far. On the basis of the synergistic antiprion effects of quinacrine and iminodibenzyl derivatives, we introduce a novel class of potential pharmaceuticals representing structural chimeras of quinacrine and imipramine analogues. We describe the chemical synthesis and bioassays of a focused library of these compounds. The most potent target compound 2a revealed an EC50 value of 20 nM determined with a cell model of prion disease, thus substantially improving the antiprion efficacy of quinacrine.
    DOI:
    10.1021/jm060773j
  • 作为产物:
    描述:
    亚氨基二苄 在 sodium carbonate 、 sodium amide 、 sodium iodide 作用下, 以 甲苯乙腈 为溶剂, 反应 53.5h, 生成 4-{4-[3-(10,11-dihydrodibenzo[b,f]azepin-5-yl)propyl]piperazin-1-yl}butyronitrile
    参考文献:
    名称:
    A Chimeric Ligand Approach Leading to Potent Antiprion Active Acridine Derivatives:  Design, Synthesis, and Biological Investigations
    摘要:
    Human transmissible neurodegenerations including Creutzfeldt-Jakob disease are unique, since they are caused by prions, an infectious agent that replicates without nucleic acids but instead by inducing conversion of a host-resident normal prion protein to a misfolded conformational isoform. For pharmacotherapy of these unusual diseases, tricyclic heterocyclic compounds such as quinacrine have been considered, but with ambiguous success in vivo, so far. On the basis of the synergistic antiprion effects of quinacrine and iminodibenzyl derivatives, we introduce a novel class of potential pharmaceuticals representing structural chimeras of quinacrine and imipramine analogues. We describe the chemical synthesis and bioassays of a focused library of these compounds. The most potent target compound 2a revealed an EC50 value of 20 nM determined with a cell model of prion disease, thus substantially improving the antiprion efficacy of quinacrine.
    DOI:
    10.1021/jm060773j
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文献信息

  • 9-AMINO-ACRIDINE DERIVATIVES AND THEIR USE FOR ELIMINATING MISFOLDED PROTEINS
    申请人:Korth Carsten
    公开号:US20090124001A1
    公开(公告)日:2009-05-14
    The invention relates to compounds according to general formula (1) and/or their enantiomers, diastereomers as well as their pharmaceutically compatible salts, and to the use thereof for producing a medicament suited for treating diseases associated with misfolded proteins.
    本发明涉及通式(1)的化合物和/或其对映体,非对映异构体以及其药学上相容的盐,以及将其用于制备适用于治疗与错折蛋白相关的疾病的药物。
  • 9-amino-acridine derivatives and their use for eliminating misfolded proteins
    申请人:——
    公开号:US07951796B2
    公开(公告)日:2011-05-31
    The invention relates to compounds according to general formula (1) and/or their enantiomers, diastereomers as well as their pharmaceutically compatible salts, and to the use thereof for producing a medicament suited for treating diseases associated with misfolded proteins.
    本发明涉及通式(1)的化合物及其对映体、非对映体异构体以及其药学上相容的盐,并且涉及将其用于制备适用于治疗与错折蛋白相关的疾病的药物。
  • 9-AMINO-ACRIDINE DERIVATIVES AND METHOD OF TREATING AUTOIMMUNE DISEASES USING THE SAME
    申请人:Korth Carsten
    公开号:US20090209516A1
    公开(公告)日:2009-08-20
    The invention relates to compounds according to general formula (1) and/or their enantiomers, diastereomers, and their pharmaceutically compatible salts, and their use to manufacture a medication as well as medications. The compounds are suited for treatment of diseases connected with misfolded proteins.
    本发明涉及通式(1)及/或其对映体、二对映异构体及其药学上相容的盐,以及它们的用途制造药物以及药物。该化合物适用于治疗与蛋白质错折相关的疾病。
  • WO2006/92395
    申请人:——
    公开号:——
    公开(公告)日:——
  • US7951796B2
    申请人:——
    公开号:US7951796B2
    公开(公告)日:2011-05-31
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