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5-methyl-4H-chromen-3-one | 1337859-45-6

中文名称
——
中文别名
——
英文名称
5-methyl-4H-chromen-3-one
英文别名
——
5-methyl-4H-chromen-3-one化学式
CAS
1337859-45-6
化学式
C10H10O2
mdl
——
分子量
162.188
InChiKey
XJRMPSKVILTCCF-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):
    1.8
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • DERIVATIVES OF 4-PIPERAZIN-1-YL-4-BENZO[B]THIOPHENE SUITABLE FOR THE TREATMENT OF CNS DISORDERS
    申请人:YAMASHITA Hiroshi
    公开号:US20120028920A1
    公开(公告)日:2012-02-02
    A heterocyclic compound or a salt thereof represented by the formula (1): where R 2 represents a hydrogen atom or a lower alkyl group; A represents a lower alkylene group or lower alkenylene group; and R 1 represents an aromatic group or a heterocyclic group. The compound of the present invention has a wide treatment spectrum for mental disorders including central nervous system disorders, no side effects and high safety.
    一种由式(1)所表示的杂环化合物或其盐:其中R2代表氢原子或较低的烷基基团;A代表较低的烷基烯基基团;R1代表芳香基团或杂环基团。本发明的化合物具有广泛的治疗精神障碍的光谱,包括中枢神经系统障碍,无副作用且安全性高。
  • BIARYL-SPIROAMINOOXZAOLINE ANALOGUES AS ALPHA 2C ADRENERGIC RECEPTOR MODULATORS
    申请人:Merck Sharp & Dohme Corp.
    公开号:US20130225582A1
    公开(公告)日:2013-08-29
    In its many embodiments, the present invention provides a novel class of biaryl spiroaminooxazoline analogues as modulators of α2C adrenergic receptor agonists, methods of preparing such compounds, pharmaceutical compositions containing one or more such compounds, methods of preparing pharmaceutical formulations comprising one or more such compounds, and methods of treatment, prevention, inhibition, or amelioration of one or more conditions associated with the α2C adrenergic receptors using such compounds or pharmaceutical compositions.
    在其多种实施方式中,本发明提供了一种新型的双芳基螺环氧唑啉类似物,作为α2C肾上腺素能受体激动剂的调节剂,制备这种化合物的方法,包含一种或多种这种化合物的制药组合物,制备包含一种或多种这种化合物的制药配方的方法,以及使用这种化合物或制药组合物治疗、预防、抑制或改善与α2C肾上腺素能受体相关的一种或多种病症的方法。
  • AMIDE COMPOUNDS
    申请人:Nozawa Eisuke
    公开号:US20110028463A1
    公开(公告)日:2011-02-03
    [Problems] To provide a compound that is useful as an agent for treating chronic renal insufficiency or an agent for treating diabetic nephropathy. [Means for Solving Problems] The present inventors have conducted extensive studies on a compound having an EP4 receptor antagonistic action, and as a result, they have found that various amide derivatives having a carboxylic group or an equivalent thereof exhibit an excellent EP4 receptor antagonistic action, thereby completing the present invention. Since the compound of the present invention has an excellent EP4 receptor antagonistic action, it is useful as an agent for preventing and/or treating chronic renal insufficiency or diabetic nephropathy.
    【问题】提供一种可用作治疗慢性肾功能不全或糖尿病肾病的药物化合物。 【解决问题的方法】本发明者对具有EP4受体拮抗作用的化合物进行了广泛的研究,结果发现具有羧酸基或其等效物的各种酰胺衍生物表现出优异的EP4受体拮抗作用,从而完成了本发明。由于本发明的化合物具有优异的EP4受体拮抗作用,因此可用作预防和/或治疗慢性肾功能不全或糖尿病肾病的药物。
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