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6,6,8,8,10,10-d6-6,7,8,9-tetrahydro-5H-tetrazolo[1,5-a]azepine | 1408250-25-8

中文名称
——
中文别名
——
英文名称
6,6,8,8,10,10-d6-6,7,8,9-tetrahydro-5H-tetrazolo[1,5-a]azepine
英文别名
5,5,7,7,9,9-Hexadeuterio-6,8-dihydrotetrazolo[1,5-a]azepine;5,5,7,7,9,9-hexadeuterio-6,8-dihydrotetrazolo[1,5-a]azepine
6,6,8,8,10,10-d6-6,7,8,9-tetrahydro-5H-tetrazolo[1,5-a]azepine化学式
CAS
1408250-25-8
化学式
C6H10N4
mdl
——
分子量
144.125
InChiKey
CWRVKFFCRWGWCS-CNGVIXCCSA-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):
    0.1
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    43.6
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    4,4-Dideutero-cyclohexanon 在 sodium azide 、 四氯化硅重水potassium carbonate 作用下, 以 乙腈 为溶剂, 反应 76.0h, 生成 6,6,8,8,10,10-d6-6,7,8,9-tetrahydro-5H-tetrazolo[1,5-a]azepine
    参考文献:
    名称:
    [EN] PENTYLENETETRAZOLE DERIVATIVES
    [FR] DÉRIVÉS DE PENTYLÈNETÉTRAZOLE
    摘要:
    提供的化合物具有以下式I的结构:( l ) 其中R1、R2、R3、R4、R5、R6、R7、R8、R9和R10如本文所述,或其药用盐。还提供包含这些化合物的药物组合物及其使用方法,例如用于治疗老年痴呆、老年混淆、精神病、神经症,当焦虑和紧张存在时,脑动脉硬化、恶心、抑郁、疲劳、虚弱、轻微行为障碍、易怒、情绪不稳定、反社会态度、焦虑、眩晕或失禁,或其症状,或用于改善个体的认知功能,例如用于唐氏综合症患者和其他情况的个体。
    公开号:
    WO2012151343A1
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文献信息

  • US20140343040A1
    申请人:——
    公开号:US20140343040A1
    公开(公告)日:2014-11-20
  • PENTYLENETETRAZOLE DERIVATIVES
    申请人:Balance Therapeutics, Inc.
    公开号:US20170044165A1
    公开(公告)日:2017-02-16
    Provided are compounds having formula I: wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , and R 10 are as disclosed herein, or a pharmaceutically salt thereof. Pharmaceutical compositions comprising the compounds and methods of their use, for instance in treating senility, senile confusion, psychoses, psychoneuroses when anxiety and nervous tension were present, cerebral arteriosclerosis, nausea, depression, fatigue, debilitation, mild behavioral disorders, irritability, emotional instability, antisocial attitudes, anxiety, vertigo or incontinence, or symptom thereof, or in improving cognitive function in individuals, for instance, in individuals with Down syndrome and other conditions, are also provided.
  • US9453020B2
    申请人:——
    公开号:US9453020B2
    公开(公告)日:2016-09-27
  • [EN] TREATING NEUROMUSCULAR OR NEUROLOGIC DISEASE THROUGH REDUCING GABAERGIC AND/OR GLYCINERGIC INHIBITORY NEUROTRANSMITTER OVERSTIMULATION<br/>[FR] TRAITEMENT DE MALADIE NEUROMUSCULAIRE OU NEUROLOGIQUE PAR RÉDUCTION DE LA SURSTIMULATION DES NEUROTRANSMETTEURS INHIBITEURS GABAERGIQUES ET/OU GLYCINERGIQUE
    申请人:RY PHARMA B V
    公开号:WO2016114655A1
    公开(公告)日:2016-07-21
    The disclosure provides novel methods of treating neuromuscular or neurologic disease, for example, Amyotrophic lateral sclerosis (ALS), through reducing GABAergic and Glycinergic inhibitory neurotransmitter activity overstimulation. Pharmaceutical compositions comprising one or more compounds capable of reducing Glycinergic activity and/or one or more compounds capable of reducing GABAergic activity are also provided. Methods for treating one or more symptoms caused by inhibitory neurotransmitter overstimulation (e.g., muscle wasting, loss of muscle function, loss of muscle coordination, respiratory depression, dysphagia, dysarthria, eye movement difficulties, oculomotor gaze palsy, supranuclear gaze palsy, bladder dysfunction and gastrointestinal dysfunction) in an individual afflicted with ALS or an ALS- like disorder are also provided.
  • [EN] TREATING NEUROMUSCULAR OR NEUROLOGIC DISEASE THROUGH REDUCING GABAERGIC AND/OR GLYCINERGIC INHIBITORY NEUROTRANSMITTER OVERSTIMULATION<br/>[FR] TRAITEMENT DE MALADIE NEUROMUSCULAIRE OU NEUROLOGIQUE PAR RÉDUCTION DE LA SURSTIMULATION DES NEUROTRANSMETTEURS INHIBITEURS GABAERGIQUES ET/OU GLYCINERGIQUES
    申请人:RY PHARMA B V
    公开号:WO2017065602A1
    公开(公告)日:2017-04-20
    The disclosure provides novel methods of treating neuromuscular or neurologic disease, for example, Amyotrophic lateral sclerosis (ALS), through reducing GABAergic and Glycinergic inhibitory neurotransmitter activity overstimulation. Pharmaceutical compositions comprising one or more compounds capable of reducing Glycinergic activity and/or one or more compounds capable of reducing GABAergic activity are also provided. Pharmaceutical compositions comprising Penicillin G and, optionally, glucocorticoid are especially useful in the present invention. Methods for treating one or more symptoms caused by inhibitory neurotransmitter overstimulation (e.g., muscle wasting, loss of muscle function, loss of muscle coordination, respiratory depression, dysphagia, dysarthria, eye movement difficulties, oculomotor gaze palsy, supranuclear gaze palsy, bladder dysfunction and gastrointestinal dysfunction) in an individual afflicted with ALS or an ALS- like disorder are also provided.
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