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3-(N-benzyl-4-piperidinyl)-1-(3-nitro-4-acetamidophenyl)-2-propen-1-one

中文名称
——
中文别名
——
英文名称
3-(N-benzyl-4-piperidinyl)-1-(3-nitro-4-acetamidophenyl)-2-propen-1-one
英文别名
3-[1-(1-phenylmethyl)-4-piperidinyl]-1-(3-nitro-4-acetamido-phenyl)2-propen-1-one;N-[4-[(E)-3-(1-benzylpiperidin-4-yl)prop-2-enoyl]-2-nitrophenyl]acetamide
3-(N-benzyl-4-piperidinyl)-1-(3-nitro-4-acetamidophenyl)-2-propen-1-one化学式
CAS
——
化学式
C23H25N3O4
mdl
——
分子量
407.469
InChiKey
WEEMGONVPXEFAP-JXMROGBWSA-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):
    3.7
  • 重原子数:
    30
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    95.2
  • 氢给体数:
    1
  • 氢受体数:
    5

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

  • 作为反应物:
    描述:
    3-(N-benzyl-4-piperidinyl)-1-(3-nitro-4-acetamidophenyl)-2-propen-1-oneplatinum(IV) oxide 氢气 作用下, 以 乙醇 为溶剂, 反应 1.0h, 以100%的产率得到1-(3-amino-4-acetamidophenyl)-3-(N-benzyl-4-piperidinyl)propan-1-one
    参考文献:
    名称:
    Design and Synthesis of 1-Heteroaryl-3-(1-benzyl-4-piperidinyl)propan-1-one Derivatives as Potent, Selective Acetylcholinesterase Inhibitors
    摘要:
    Herein is described the synthesis and structure-activity relationship of a novel series of aromatic and heteroaromatic 3-(1-benzyl-4-piperidinyl)propan-1-one derivatives that display potent and selective inhibition of the enzyme acetylcholinesterase (AChE). 1-(2-Methyl-6-benzothiazolyl)-3-(N-benzyl-4-piperidinyl)propan-1-one hydrochloride, 6d, is one of the most active compounds within this series exhibiting an IC50 for the inhibition of the AChE enzyme equal to 6.8 nM. Compound 6d has shown a dose-dependent elevation of total acetylcholine (ACh) levels in the mouse forebrain with an oral ED(50) = 9.8 mg/kg. In addition, in vivo microdialysis experiments in the rat demonstrate that 6d increases extracellular ACh (100% over basal) 1-3 h postdose with an oral ED(50) = 4.8 mg/kg.
    DOI:
    10.1021/jm00007a005
  • 作为产物:
    描述:
    1-苄基-4-哌啶甲醛4-乙酰氨基-3-硝基苯乙酮正丁基锂 作用下, 以 四氢呋喃正己烷 为溶剂, 反应 1.0h, 以25%的产率得到3-(N-benzyl-4-piperidinyl)-1-(3-nitro-4-acetamidophenyl)-2-propen-1-one
    参考文献:
    名称:
    Design and Synthesis of 1-Heteroaryl-3-(1-benzyl-4-piperidinyl)propan-1-one Derivatives as Potent, Selective Acetylcholinesterase Inhibitors
    摘要:
    Herein is described the synthesis and structure-activity relationship of a novel series of aromatic and heteroaromatic 3-(1-benzyl-4-piperidinyl)propan-1-one derivatives that display potent and selective inhibition of the enzyme acetylcholinesterase (AChE). 1-(2-Methyl-6-benzothiazolyl)-3-(N-benzyl-4-piperidinyl)propan-1-one hydrochloride, 6d, is one of the most active compounds within this series exhibiting an IC50 for the inhibition of the AChE enzyme equal to 6.8 nM. Compound 6d has shown a dose-dependent elevation of total acetylcholine (ACh) levels in the mouse forebrain with an oral ED(50) = 9.8 mg/kg. In addition, in vivo microdialysis experiments in the rat demonstrate that 6d increases extracellular ACh (100% over basal) 1-3 h postdose with an oral ED(50) = 4.8 mg/kg.
    DOI:
    10.1021/jm00007a005
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文献信息

  • Heteroaryl amines as novel acetylcholinesterase inhibitors
    申请人:——
    公开号:US20020049210A1
    公开(公告)日:2002-04-25
    Compounds of the formula 1 wherein ring A, ring B, ring D, R 2 , R 3 , R 4 , R 5 , R 6 ,R 11 , R 12 , R 13 , E, G, X and P are as defined below. The compounds of formula I are cholinesterase inhibitors and are useful in enhancing memory in patients suffering from dementia and Alzheimer's disease.
    化合物的公式为1,其中环A、环B、环D、R2、R3、R4、R5、R6、R11、R12、R13、E、G、X和P的定义如下。式I的化合物是胆碱酯酶抑制剂,对于患有痴呆症和阿尔茨海默病的患者增强记忆力具有有用的作用。
  • US5574046A
    申请人:——
    公开号:US5574046A
    公开(公告)日:1996-11-12
  • US5965574A
    申请人:——
    公开号:US5965574A
    公开(公告)日:1999-10-12
  • US6124321A
    申请人:——
    公开号:US6124321A
    公开(公告)日:2000-09-26
  • US6303633B1
    申请人:——
    公开号:US6303633B1
    公开(公告)日:2001-10-16
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