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3-ethanoyl-5-methanesulfonyl-benzoic acid methyl ester | 198477-85-9

中文名称
——
中文别名
——
英文名称
3-ethanoyl-5-methanesulfonyl-benzoic acid methyl ester
英文别名
methyl 3-acetyl-5-methylsulfonylbenzoate
3-ethanoyl-5-methanesulfonyl-benzoic acid methyl ester化学式
CAS
198477-85-9
化学式
C11H12O5S
mdl
——
分子量
256.279
InChiKey
XATQASSZJCWJQL-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):
    0.7
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    85.9
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    C15H20O5S 在 盐酸 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 3-ethanoyl-5-methanesulfonyl-benzoic acid methyl ester
    参考文献:
    名称:
    Synthesis and SAR of hydroxyethylamine based phenylcarboxyamides as inhibitors of BACE
    摘要:
    A series of N-((2S,3R)-1-(3,5-difluorophenyl)-3-hydroxy-4-(3-methoxybenzylamino)-butan-2-yl)benzamides has been synthesized as BACE inhibitors. A variety of P2 and P3 substituents has been explored, and these efforts have culminated in the identification of several 1,3,5-trisubstituted phenylcarboxyamides with potent BACE inhibitory activity. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.03.144
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文献信息

  • Novel phenylcarboxyamides as beta-secretase inhibitors
    申请人:Wu Yong-Jin
    公开号:US20070032470A1
    公开(公告)日:2007-02-08
    There is provided a series of novel phenylcarboxyamides of Formula (I) or a stereoisomer; or a pharmaceutically acceptable salt thereof, wherein R 1 , R 2 , R 3 , X and Y as defined herein, their pharmaceutical compositions and methods of use. These novel compounds inhibit the processing of amyloid precursor protein (APP) by β-secretase and, more specifically, inhibit the production of Aβ-peptide. The present disclosure is directed to compounds useful in the treatment of neurological disorders related to β-amyloid production, such as Alzheimer's disease and other conditions affected by anti-amyloid activity.
    提供了一系列新颖的苯基羧酰胺化合物,其化学式为(I)或其立体异构体;或其药用可接受的盐,其中R1、R2、R3、X和Y的定义如本文所述,它们的药物组成和使用方法。这些新颖化合物抑制β-分泌酶对淀粉样前体蛋白(APP)的加工,更具体地说,抑制Aβ肽的产生。本公开涉及对β-淀粉样蛋白产生相关的神经系统疾病的治疗中有用的化合物,如阿尔茨海默病和其他受抗淀粉样活性影响的疾病。
  • Compounds to treat Alzheimer's disease
    申请人:Fang Y. Lawrence
    公开号:US20070213407A1
    公开(公告)日:2007-09-13
    The present invention is substituted amines of formula (X) useful in treating Alzheimer's disease and other similar diseases.
    本发明涉及一种公式(X)的取代胺,用于治疗阿尔茨海默病和其他类似疾病。
  • Substituted Hydroxyethylamines
    申请人:Tenbrink Ruth
    公开号:US20080096942A1
    公开(公告)日:2008-04-24
    Disclosed are compounds of the formula and the pharmaceutically acceptable salts thereof wherein the variables G, L, A, W, E, R2, R2, R4, R5, R N , and R C are defined herein. These compounds interact with and inhibit the activity of the enzyme beta-secretase. These compounds are therefore useful in treating Alzheimer's disease and other similar diseases. Pharmaceutical compositions and methods of treatment of these diseases are also disclosed.
    本发明涉及公式所示的化合物及其药学上可接受的盐,其中变量G、L、A、W、E、R2、R2、R4、R5、RN和RC的定义如本文所述。这些化合物与酶β-分泌酶相互作用并抑制其活性。因此,这些化合物在治疗阿尔茨海默病和其他类似疾病方面是有用的。本发明还涉及这些疾病的制药组合物和治疗方法。
  • US5679712A
    申请人:——
    公开号:US5679712A
    公开(公告)日:1997-10-21
  • US5849775A
    申请人:——
    公开号:US5849775A
    公开(公告)日:1998-12-15
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