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N-(1,3-benzodioxol-5-yl)-2-methylpropanamide

中文名称
——
中文别名
——
英文名称
N-(1,3-benzodioxol-5-yl)-2-methylpropanamide
英文别名
——
N-(1,3-benzodioxol-5-yl)-2-methylpropanamide化学式
CAS
——
化学式
C11H13NO3
mdl
MFCD00709751
分子量
207.23
InChiKey
RYSGOAPHCXQSDW-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:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.363
  • 拓扑面积:
    47.6
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • Azetidinone Derivatives and Methods of Use Thereof
    申请人:Aslanian G. Robert
    公开号:US20080076751A1
    公开(公告)日:2008-03-27
    The present invention relates to Azetidinone Derivatives, compositions comprising an Azetidinone Derivative and methods for treating or preventing a disorder of lipid metabolism, pain, diabetes, a vascular condition, demyelination or nonalcoholic fatty liver disease, comprising administering to a patient an effective amount of an Azetidinone Derivative.
    本发明涉及吲哚酮衍生物,包含吲哚酮衍生物的组合物以及治疗或预防脂质代谢紊乱、疼痛、糖尿病、血管疾病、脱髓鞘病或非酒精性脂肪肝病的方法,包括向患者投予有效量的吲哚酮衍生物
  • Therapeutic compounds and uses thereof
    申请人:GENENTECH, INC.
    公开号:US10206931B2
    公开(公告)日:2019-02-19
    The present invention relates to compounds of formula (I): and to salts thereof, wherein A has any of the values defined in the specification, and compositions and uses thereof. The compounds are useful as inhibitors of CBP and/or EP300. Also included are pharmaceutical compositions comprising a compound of formula (I) or a pharmaceutically acceptable salt thereof, and methods of using such compounds and salts in the treatment of various CBP and/or EP300-mediated disorders.
    本发明涉及式(I)化合物: 及其盐,其中 A 具有说明书中定义的任一值,以及其组合物和用途。这些化合物可用作 CBP 和/或 EP300 的抑制剂。还包括包含式(I)化合物或其药学上可接受的盐的药物组合物,以及使用此类化合物和盐治疗各种CBP和/或EP300介导的疾病的方法。
  • METHOD OF INDUCING NEGATIVE CHEMOTAXIS
    申请人:Goodhew Erica Brook
    公开号:US20100093747A1
    公开(公告)日:2010-04-15
    The current invention is directed to methods of inducing the negative chemotaxis of a migratory cell comprising contacting the cell with a compound having the Formula (I), (II), (III) or (IV).
  • SUBSTITUTED BRIDGED UREA ANALOGS AS SIRTUIN MODULATORS
    申请人:GlaxoSmithKline Intellectual Property (No.2) Limited
    公开号:US20170355705A1
    公开(公告)日:2017-12-14
    The present invention relates to novel substituted bridged urea analog compounds of Formula (I) or pharmaceutically acceptable salts thereof, corresponding pharmaceutical compositions, processes for making and use of such compounds, alone or in combination with other therapeutic agents, as Sirtuin Modulators useful for increasing lifespan of a cell, and for use in treating and/or preventing a wide variety of diseases and disorders, which include, but are not limited to, for example, diseases or disorders related to aging or stress, diabetes, obesity, neurodegenerative diseases, cardiovascular disease, blood clotting disorders, inflammation, cancer, and/or flushing as well as diseases or disorders that would benefit from increased mitochondrial activity.
  • THERAPEUTIC COMPOUNDS AND USES THEREOF
    申请人:GENENTECH, INC.
    公开号:US20170312292A1
    公开(公告)日:2017-11-02
    The present invention relates to compounds of formula (I): and to salts thereof, wherein A has any of the values defined in the specification, and compositions and uses thereof. The compounds are useful as inhibitors of CBP and/or EP300. Also included are pharmaceutical compositions comprising a compound of formula (I) or a pharmaceutically acceptable salt thereof, and methods of using such compounds and salts in the treatment of various CBP and/or EP300-mediated disorders.
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