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5-(o-Tolyl)thiazole-4-carboxylic acid | 1047676-34-5

中文名称
——
中文别名
——
英文名称
5-(o-Tolyl)thiazole-4-carboxylic acid
英文别名
5-(2-methylphenyl)-1,3-thiazole-4-carboxylic acid
5-(o-Tolyl)thiazole-4-carboxylic acid化学式
CAS
1047676-34-5
化学式
C11H9NO2S
mdl
——
分子量
219.264
InChiKey
ACWZIZRJXYXOGD-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):
    2.8
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    78.4
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • [EN] PHENETHYLAMIDE DERIVATIVES AND THEIR HETEROCYCLIC ANALOGUES<br/>[FR] DÉRIVÉS DE PHÉNÉTHYLAMIDE ET LEURS ANALOGUES HÉTÉROCYCLIQUES
    申请人:ACTELION PHARMACEUTICALS LTD
    公开号:WO2010044054A1
    公开(公告)日:2010-04-22
    The invention relates to novel phenethylamide derivatives and their heterocyclic analogues of formula (I), wherein A, B, R1, R2 and R3 are as described in the application, and to the use of such compounds, or of pharmaceutically acceptable salts of such compounds, as medicaments, especially as orexin receptor antagonists.
    这项发明涉及新型苯乙酰胺衍生物及其异环类似物,其化学式为(I),其中A、B、R1、R2和R3如申请中所述,并且涉及将这种化合物或这种化合物的药用可接受盐用作药物,特别是促进睡眠的药物受体拮抗剂。
  • AZA-BRIDGED-RING COMPOUND
    申请人:Nagashima Shinya
    公开号:US20100105658A1
    公开(公告)日:2010-04-29
    [Problems] Provided is a compound which has an antagonistic action on a muscarinic M 3 receptor and is useful as an active ingredient of a prophylactic and/or therapeutic agent for an inflammatory disease such as a chronic obstructive pulmonary disease (COPD), asthma and the like. [Means for Solving Problems] The present inventors have made studies on a compound having an antagonistic action on the binding of a muscarinic M 3 receptor, and they have found that an aza-bridged-ring compound or a salt thereof has an antagonistic action on the binding of a muscarinic M 3 receptor, thereby completing the present invention. The aza-bridged-ring compound of the present invention has an antagonistic action on the binding of a muscarinic M 3 receptor, and can be used as a prophylactic and/or therapeutic agent for an inflammatory disease such as a chronic obstructive pulmonary disease (COPD), asthma and the like.
    【问题】提供了一种具有抗胆碱能M3受体拮抗作用的化合物,可作为预防和/或治疗慢性阻塞性肺疾病(COPD)、哮喘等炎症性疾病的活性成分。 【解决问题的手段】本发明人对具有抗胆碱能M3受体结合作用的化合物进行了研究,发现一种氮杂环桥合环化合物或其盐具有抗胆碱能M3受体结合作用,从而完成了本发明。本发明的氮杂环桥合环化合物具有抗胆碱能M3受体结合作用,并可用作预防和/或治疗慢性阻塞性肺疾病(COPD)、哮喘等炎症性疾病的预防和/或治疗剂。
  • PHENETHYLAMIDE DERIVATIVES AND THEIR HETEROCYCLIC ANALOGUES
    申请人:Actelion Pharmaceuticals Ltd.
    公开号:EP2334643A1
    公开(公告)日:2011-06-22
  • US8367696B2
    申请人:——
    公开号:US8367696B2
    公开(公告)日:2013-02-05
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