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(2R)-3-(5,6-dihydrobenzo[b][1]benzazepin-11-yl)-N,N,2-trimethylpropan-1-amine

中文名称
——
中文别名
——
英文名称
(2R)-3-(5,6-dihydrobenzo[b][1]benzazepin-11-yl)-N,N,2-trimethylpropan-1-amine
英文别名
——
(2R)-3-(5,6-dihydrobenzo[b][1]benzazepin-11-yl)-N,N,2-trimethylpropan-1-amine化学式
CAS
——
化学式
C20H26N2
mdl
——
分子量
294.4
InChiKey
ZSCDBOWYZJWBIY-MRXNPFEDSA-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):
    5.8
  • 重原子数:
    22
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    6.5
  • 氢给体数:
    0
  • 氢受体数:
    2

ADMET

代谢
(r)-三甲丙咪嗪已知的人类代谢物包括去甲基三甲丙咪嗪、11-[3-(二甲基氨基)-2-甲基丙基]-5,6-二氢苯并[b][1]苯氮杂卓-5-醇和11-[3-(二甲基氨基)-2-甲基丙基]-5,6-二氢苯并[b][1]苯氮杂卓-3-醇。
(r)-trimipramine has known human metabolites that include Desmethyltrimipramine, 11-[3-(dimethylamino)-2-methylpropyl]-5,6-dihydrobenzo[b][1]benzazepin-5-ol, and 11-[3-(Dimethylamino)-2-methylpropyl]-5,6-dihydrobenzo[b][1]benzazepin-3-ol.
来源:NORMAN Suspect List Exchange

文献信息

  • [EN] TREATMENT OF AUTISM SPECTRUM DISORDERS, OBSESSIVE-COMPULSIVE DISORDER AND ANXIETY DISORDERS<br/>[FR] TRAITEMENT DE TROUBLES DU SPECTRE AUTISTIQUE, DE TROUBLES OBSESSIVO-COMPULSIFS ET DE TROUBLES DE L'ANXIÉTÉ
    申请人:RUGEN HOLDINGS CAYMAN LTD
    公开号:WO2018098128A1
    公开(公告)日:2018-05-31
    Disclosed are methods for treating NMDA receptor-mediated disorders by administering certain NR2B subunit-selective NMDA (N methyl-D aspartate) antagonists. NMDA receptor-mediated disorders include autism spectrum disorders, obsessive-compulsive disorder and anxiety disorders.
    揭示了通过给予特定NR2B亚单位选择性NMDA(N-甲基-D-天冬氨酸)拮抗剂来治疗NMDA受体介导的疾病的方法。NMDA受体介导的疾病包括自闭症谱系障碍、强迫症和焦虑症。
  • [EN] TREATMENT OF ANXIETY DISORDERS AND AUTISM SPECTRUM DISORDERS<br/>[FR] TRAITEMENT DES TROUBLES DE L'ANXIÉTÉ ET DES TROUBLES DU SPECTRE AUTISTIQUE
    申请人:RUGEN HOLDINGS CAYMAN LTD
    公开号:WO2016049048A1
    公开(公告)日:2016-03-31
    Disclosed are methods for treating autism spectrum disorders and/or anxiety disorders by administering certain NR2B subunit-selective NMDA (N methyl-D aspartate) antagonists. Anxiety disorders include agoraphobia (with or without panic disorder), generalized anxiety disorder (GAD), social anxiety disorder (SAD), panic disorder (PD), post-traumatic stress disorder (PTSD) and obsessive-compulsive disorder (OCD).
    本文披露了通过给予特定NR2B亚单位选择性NMDA(N-甲基-D-天冬氨酸)拮抗剂来治疗自闭症谱系障碍和/或焦虑障碍的方法。焦虑障碍包括广场恐惧症(伴有或不伴有惊恐障碍)、广泛性焦虑障碍(GAD)、社交焦虑障碍(SAD)、惊恐障碍(PD)、创伤后应激障碍(PTSD)和强迫症(OCD)。
  • Piperazine derivatives and the use thereof as medicament
    申请人:HOENKE Christoph
    公开号:US20150105397A1
    公开(公告)日:2015-04-16
    The present inventions relate to substituted piperazine derivatives of general formula (I) and to the manufacture of said compounds, pharmaceutical compositions comprising a compound according to general formula (I), and the use of said compounds for the treatment of various medical conditions related to glycine transporter-1 (GlyT1).
    这些发明涉及一般式(I)的取代哌嗪衍生物,以及所述化合物的制备,包括符合一般式(I)的化合物的药物组合物,以及利用这些化合物治疗与甘氨酸转运蛋白-1(GlyT1)相关的各种医疗状况。
  • Inhibitors of protein kinases
    申请人:Zeitlmann Lutz
    公开号:US20110224225A1
    公开(公告)日:2011-09-15
    Compounds of general Formula (I): wherein R 1 , R 2 , R 3 , R a , A, B and x are as defined herein are inhibitors of protein kinases in particular members of the cyclin-dependent kinase family and/or the glycogen synthase kinase 3 family and are useful in preventing and/or treating any type of pain, inflammatory disorders, cancer, immunological diseases, proliferative diseases, infectious diseases, cardiovascular diseases, metabolic disorders, renal diseases, neurologic and neuropsychiatric diseases and neurodegenerative diseases.
    通用式(I)的化合物: 其中R1、R2、R3、Ra、A、B和x的定义如本文所述,是特定于细胞周期蛋白激酶家族和/或糖原合成酶激酶3家族的抑制剂,并且在预防和/或治疗任何类型的疼痛、炎症性疾病、癌症、免疫性疾病、增殖性疾病、传染病、心血管疾病、代谢性疾病、肾脏疾病、神经和神经精神疾病以及神经退行性疾病方面具有用处。
  • Novel Bicyclic Pyridinones
    申请人:Pettersson Martin Youngjin
    公开号:US20120252758A1
    公开(公告)日:2012-10-04
    Compounds and pharmaceutically acceptable salts of the compounds are disclosed, wherein the compounds have the structure of Formula I as defined herein. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.
    所述化合物及其药用可接受的盐被披露,其中所述化合物具有如本文所定义的Formula I的结构。相应的药物组合物、治疗方法、合成方法和中间体也被披露。
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