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methyl N'-(4-phenyl-1,3-thiazol-2-yl)imidothiocarbamate hydroiodide | 863657-69-6

中文名称
——
中文别名
——
英文名称
methyl N'-(4-phenyl-1,3-thiazol-2-yl)imidothiocarbamate hydroiodide
英文别名
methyl N'-(4-phenyl-1,3-thiazol-2-yl)carbamimidothioate;hydroiodide
methyl N'-(4-phenyl-1,3-thiazol-2-yl)imidothiocarbamate hydroiodide化学式
CAS
863657-69-6
化学式
C11H11N3S2*HI
mdl
——
分子量
377.273
InChiKey
PUIAHEURPPKIJW-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):
    4.14
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    105
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    methyl N'-(4-phenyl-1,3-thiazol-2-yl)imidothiocarbamate hydroiodide 生成 N-[2-methoxy-5-(trifluoromethyl)benzyl]-N'-(4-phenyl-1,3-thiazol-2-yl)guanidine
    参考文献:
    名称:
    [DE] GUANIDINVERBINDUNGEN UND IHRE VERWENDUNG ALS BINDUNGSPARTNER FÜR 5-HT5-REZEPTOREN
    [EN] GUANIDINE COMPOUNDS, AND USE THEREOF AS BINDING PARTNERS FOR 5-HT5 RECEPTORS
    [FR] COMPOSES DE GUANIDINE ET LEUR UTILISATION COMME ELEMENTS DE LIAISON POUR LES RECEPTEURS 5-HT5
    摘要:
    公开号:
    WO2005082871A3
  • 作为产物:
    参考文献:
    名称:
    [DE] GUANIDINVERBINDUNGEN UND IHRE VERWENDUNG ALS BINDUNGSPARTNER FÜR 5-HT5-REZEPTOREN
    [EN] GUANIDINE COMPOUNDS, AND USE THEREOF AS BINDING PARTNERS FOR 5-HT5 RECEPTORS
    [FR] COMPOSES DE GUANIDINE ET LEUR UTILISATION COMME ELEMENTS DE LIAISON POUR LES RECEPTEURS 5-HT5
    摘要:
    公开号:
    WO2005082871A3
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文献信息

  • Guanidine Compounds, and Use Thereof as Binding partners for 5-Ht5 Receptors
    申请人:Netz Astrid
    公开号:US20070299074A1
    公开(公告)日:2007-12-27
    The present invention relates to guanidine compounds of the general formula I corresponding enantiomeric, diastereomeric and/or tautomeric forms thereof as well as pharmaceutically acceptable salts thereof. The present compound further relates to the use of guanidine compounds as binding partners for 5-HT5 receptors for the treatment of diseases which are modulated by a 5-HT5 receptor activity, in particular for the treatment of neurodegenerative and neuropsychiatric disorders as well as the associated signs, symptoms and dysfunctions.
    本发明涉及通式I的化合物及其对应的对映异构体、顺反异构体和/或互变异构体,以及其药学上可接受的盐。本化合物进一步涉及化合物作为5-HT5受体的结合伴侣,用于治疗受5-HT5受体活性调节的疾病,特别是用于治疗神经退行性和神经精神障碍以及相关的症状、症候和功能障碍。
  • GUANIDINE COMPOUNDS, AND USE THEREOF AS BINDING PARTNERS FOR 5-HT5 RECEPTORS
    申请人:Netz Astrid
    公开号:US20110237589A1
    公开(公告)日:2011-09-29
    The present invention relates to guanidine compounds of the general formula I corresponding enantiomeric, diastereomeric and/or tautomeric forms thereof as well as pharmaceutically acceptable salts thereof. The present compound further relates to the use of guanidine compounds as binding partners for 5-HT5 receptors for the treatment of diseases which are modulated by a 5-HT5 receptor activity, in particular for the treatment of neurodegenerative and neuropsychiatric disorders as well as the associated signs, symptoms and dysfunctions.
    本发明涉及一般式I的化合物,其对应的对映异构体、顺反异构体和/或互变异构体以及其药学上可接受的盐。本化合物进一步涉及将化合物用作5-HT5受体的结合伴侣,用于治疗由5-HT5受体活性调节的疾病,特别是用于治疗神经退行性和神经精神障碍以及相关的症状、症候和功能障碍。
  • GUANIDINE COMPOUNDS AND USE THEREOF AS BINDING PARTNERS FOR 5-HT5 RECEPTORS
    申请人:ABBVIE DEUTSCHLAND GMBH & CO. KG
    公开号:US20170037016A1
    公开(公告)日:2017-02-09
    The present invention relates to guanidine compounds of the general formula I corresponding enantiomeric, diastereomeric and/or tautomeric forms thereof as well as pharmaceutically acceptable salts thereof. The present compound further relates to the use of guanidine compounds as binding partners for 5-HT5 receptors for the treatment of diseases which are modulated by a 5-HT5 receptor activity, in particular for the treatment of neurodegenerative and neuropsychiatric disorders as well as the associated signs, symptoms and dysfunctions.
  • US8431604B2
    申请人:——
    公开号:US8431604B2
    公开(公告)日:2013-04-30
  • US8481576B2
    申请人:——
    公开号:US8481576B2
    公开(公告)日:2013-07-09
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