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2-(3-benzyloxy)phenyl-3-(2-piperidin-1-ylethyl)-2,3-dihydrobenzo-1,3-thiazin-4-one

中文名称
——
中文别名
——
英文名称
2-(3-benzyloxy)phenyl-3-(2-piperidin-1-ylethyl)-2,3-dihydrobenzo-1,3-thiazin-4-one
英文别名
2-(3-phenylmethoxyphenyl)-3-(2-piperidin-1-ylethyl)-2H-1,3-benzothiazin-4-one
2-(3-benzyloxy)phenyl-3-(2-piperidin-1-ylethyl)-2,3-dihydrobenzo-1,3-thiazin-4-one化学式
CAS
——
化学式
C28H30N2O2S
mdl
——
分子量
458.624
InChiKey
NNAAOXHOKAQFNC-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):
    5.6
  • 重原子数:
    33
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    58.1
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    参考文献:
    名称:
    [EN] 2-SUBSTITUTED BICYCLIC BENZOHETEROCYCLIC COMPOUNDS AND THEIR USE AS SODIUM CHANNEL BLOCKERS
    [FR] COMPOSES BENZOHETEROCYCLIQUES BICYCLIQUES SUBSTITUES EN 2 ET LEUR UTILISATION EN TANT QUE BLOQUEURS DU CANAL SODIQUE
    摘要:
    本发明涉及一种治疗对钠离子通道阻滞具有反应的疾病的方法,使用新型的2-取代的双环苯杂环化合物,其化学式为I,或其药学上可接受的盐或溶剂,其中X为-NH-,-N=或-S-,Y为氧或硫,n,p,R1,R2,R3和R4在规范中有定义。该发明还涉及化合物I用于治疗全球性或局部性缺血后的神经损伤,用于治疗或预防神经退行性疾病,如肌萎缩侧索硬化症(ALS),以及用于治疗、预防或改善急性或慢性疼痛、神经病性疼痛或手术疼痛,作为抗耳鸣剂,抗癫痫药,抗躁狂抑郁药,局部麻醉剂,抗心律失常药以及治疗或预防糖尿病性神经病变。
    公开号:
    WO2004013111A1
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文献信息

  • 2-substituted bicyclic benzoheterocyclic compounds and their use as sodium channel blockers
    申请人:Euro-Celtique S.A.
    公开号:US20040152696A1
    公开(公告)日:2004-08-05
    This invention relates to a method of treating disorders responsive to the blockade of sodium ion channels using novel 2-substituted bicyclic benzoheterocyclic compounds of Formula I: 1 or a pharmaceutically-acceptable salt or solvate thereof, wherein X is —NH—, —N═ or —S—, Y is oxygen or sulfur, and n, p, R 1 , R 2 , R 3 and R 4 are defined in the specification. The invention is also directed to the use of compounds of Formula I for the treatment of neuronal damage following global or focal ischemia, for the treatment or prevention of neurodegenerative conditions such as amyotrophic lateral sclerosis (ALS), and for the treatment, prevention or amelioration of acute or chronic pain, neuropathic pain or surgical pain, as antitinnitus agents, as anticonvulsants, and as antimanic depressants, as local anesthetics, as antiarrhythmics and for the treatment or prevention of diabetic neuropathy.
    本发明涉及使用新型2-取代双环苯并杂环化合物(公式I:1)或其药学上可接受的盐或溶剂,通过阻断钠离子通道来治疗对其敏感的疾病。其中,X为—NH—、—N═或—S—,Y为氧或硫,n、p、R1、R2、R3和R4在说明书中有定义。本发明还涉及使用公式I化合物治疗全局或局部缺血后的神经损伤,治疗或预防神经退行性疾病如肌萎缩性侧索硬化(ALS),以及治疗、预防或缓解急性或慢性疼痛、神经病理性疼痛或手术疼痛,作为抗耳鸣剂、抗癫痫药物和抗躁狂抑郁药物,作为局部麻醉剂、抗心律失常药物以及治疗或预防糖尿病神经病变的药物。
  • 2-SUBSTITUTED BICYCLIC BENZOHETEROCYCLIC COMPOUNDS AND THEIR USE AS SODIUM CHANNEL BLOCKERS
    申请人:Euro-Celtique S.A.
    公开号:EP1534690A1
    公开(公告)日:2005-06-01
  • [EN] 2-SUBSTITUTED BICYCLIC BENZOHETEROCYCLIC COMPOUNDS AND THEIR USE AS SODIUM CHANNEL BLOCKERS<br/>[FR] COMPOSES BENZOHETEROCYCLIQUES BICYCLIQUES SUBSTITUES EN 2 ET LEUR UTILISATION EN TANT QUE BLOQUEURS DU CANAL SODIQUE
    申请人:EURO CELTIQUE SA
    公开号:WO2004013111A1
    公开(公告)日:2004-02-12
    This invention relates to a method of treating disorders responsive to the blockade of sodium ion channels using novel 2-substituted bicyclic benzoheterocyclic compounds of Formula I, or a pharmaceutically-acceptable salt or solvate thereof, wherein X is -NH-, -N= or -S-, Y is oxygen or sulfur, and n, p, R1, R2, R3 and R4 are defined in the specification. The invention is also directed to the use of compounds of Formula I for the treatment of neuronal damage following global or focal ischemia, for the treatment or prevention of neurodegenerative conditions such as amyotrophic lateral sclerosis (ALS), and for the treatment, prevention or amelioration of acute or chronic pain, neuropathic pain or surgical pain, as antitinnitus agents, as anticonvulsants, and as antimanic depressants, as local anesthetics, as antiarrhythmics and for the treatment or prevention of diabetic neuropathy.
    本发明涉及一种治疗对钠离子通道阻滞具有反应的疾病的方法,使用新型的2-取代的双环苯杂环化合物,其化学式为I,或其药学上可接受的盐或溶剂,其中X为-NH-,-N=或-S-,Y为氧或硫,n,p,R1,R2,R3和R4在规范中有定义。该发明还涉及化合物I用于治疗全球性或局部性缺血后的神经损伤,用于治疗或预防神经退行性疾病,如肌萎缩侧索硬化症(ALS),以及用于治疗、预防或改善急性或慢性疼痛、神经病性疼痛或手术疼痛,作为抗耳鸣剂,抗癫痫药,抗躁狂抑郁药,局部麻醉剂,抗心律失常药以及治疗或预防糖尿病性神经病变。
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