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1-(3-fluoro-4-methylphenyl)-2-methylpropan-1-one

中文名称
——
中文别名
——
英文名称
1-(3-fluoro-4-methylphenyl)-2-methylpropan-1-one
英文别名
2,4'-Dimethyl-3'-fluoropropiophenone
1-(3-fluoro-4-methylphenyl)-2-methylpropan-1-one化学式
CAS
——
化学式
C11H13FO
mdl
——
分子量
180.222
InChiKey
NHFVNILBNTUIMR-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):
    3.1
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • NOVEL IMIDE DERIVATIVES AND USE THEREOF AS MEDICINE
    申请人:Mitsubishi Tanabe Pharma Corporation
    公开号:EP3321256A1
    公开(公告)日:2018-05-16
    Provided is a novel low-molecular-weight compound that suppresses production of induction type MMPs, particularly MMP-9, rather than production of hemostatic type MMP-2. The present invention relates to a compound represented by the following formula (I): wherein each symbol is as described in the DESCRIPTION. The compound has a selective MMP-9 production suppressive action, and is useful as a drug for the prophylaxis and/or treatment of autoimmune diseases such as rheumatoid arthritis and the like, inflammatory bowel diseases (ulcerative colitis, Crohn's disease) or osteoarthritis.
    本发明提供了一种新型低分子量化合物,它能抑制诱导型 MMP(尤其是 MMP-9)的产生,而不是抑制止血型 MMP-2 的产生。本发明涉及一种由下式(I)代表的化合物: 其中各符号如说明书所述。该化合物具有选择性抑制 MMP-9 生成的作用,可作为预防和/或治疗自身免疫性疾病(如类风湿性关节炎等)、炎症性肠病(溃疡性结肠炎、克罗恩病)或骨关节炎的药物。
  • Imide derivatives and use thereof as medicine
    申请人:MITSUBISHI TANABE PHARMA CORPORATION
    公开号:US10407408B2
    公开(公告)日:2019-09-10
    Provided is a novel low-molecular-weight compound that suppresses production of induction type MMPs, particularly MMP-9, rather than production of hemostatic type MMP-2. The present invention relates to a compound represented by the following formula (I): wherein each symbol is as described in the DESCRIPTION. The compound has a selective MMP-9 production suppressive action, and is useful as a drug for the prophylaxis and/or treatment of autoimmune diseases such as rheumatoid arthritis and the like, inflammatory bowel diseases (ulcerative colitis, Crohn's disease) or osteoarthritis.
    本发明提供了一种新型低分子量化合物,它能抑制诱导型 MMP(尤其是 MMP-9)的产生,而不是抑制止血型 MMP-2 的产生。本发明涉及一种由下式(I)代表的化合物: 其中各符号如说明书所述。该化合物具有选择性抑制 MMP-9 生成的作用,可作为预防和/或治疗类风湿性关节炎等自身免疫性疾病、炎症性肠病(溃疡性结肠炎、克罗恩病)或骨关节炎的药物。
  • NON-RETINOID ANTAGONISTS FOR TREATMENT OF AGE-RELATED MACULAR DEGENERATION AND STARGARDT DISEASE
    申请人:Petrukhin Konstantin
    公开号:US20150126494A1
    公开(公告)日:2015-05-07
    A method for treating a disease characterized by excessive lipofuscin accumulation in the retina in mammals afflicted therewith, comprising administering to the mammal an effective amount of a non-retinoid antagonist compound or a pharmaceutically acceptable salt thereof.
  • DIHYDROPYRAZOLOPYRIMIDINONE COMPOUNDS AS PDE2 INHIBITORS
    申请人:Merck Sharp & Dohme Corp.
    公开号:US20180148453A1
    公开(公告)日:2018-05-31
    The present invention is directed to dihydropyrazolopyrimidinone compounds of formula (I) which are useful as therapeutic agents for the treatment of central nervous system disorders associated with phosphodiesterase 2 (PDE2). The present invention also relates to the use of such compounds for treating neurological and psychiatric disorders, such as schizophrenia, psychosis, Parkinson's disease, Parkinson's disease dementia (PDD), or Huntington's disease, and those associated with striatal hypofunction or basal ganglia dysfunction.
  • US9333202B2
    申请人:——
    公开号:US9333202B2
    公开(公告)日:2016-05-10
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