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diethyl 1-[(3,4-dimethoxyphenyl)methyl]-4-naphthalen-1-yl-4H-pyridine-3,5-dicarboxylate | 1421235-47-3

中文名称
——
中文别名
——
英文名称
diethyl 1-[(3,4-dimethoxyphenyl)methyl]-4-naphthalen-1-yl-4H-pyridine-3,5-dicarboxylate
英文别名
——
diethyl 1-[(3,4-dimethoxyphenyl)methyl]-4-naphthalen-1-yl-4H-pyridine-3,5-dicarboxylate化学式
CAS
1421235-47-3
化学式
C30H31NO6
mdl
——
分子量
501.579
InChiKey
RZLUFXADWFWRAJ-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):
    5.4
  • 重原子数:
    37
  • 可旋转键数:
    11
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    74.3
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    1-萘甲醛3,4-二甲氧基苄胺丙炔酸乙酯溶剂黄146 作用下, 反应 0.25h, 以63.75%的产率得到diethyl 1-[(3,4-dimethoxyphenyl)methyl]-4-naphthalen-1-yl-4H-pyridine-3,5-dicarboxylate
    参考文献:
    名称:
    Discovery of novel 1,4-dihydropyridine-based PDE4 inhibitors
    摘要:
    Substituted 1,4-dihydropyridines were discovered as a novel and potent series of phosphodiesterase 4 (PDE4) inhibitors. Structure-activity relationships within this series have been carried out and studies revealed that the dihydropyridine core, with indole moiety and 3,4-dimethoxybenzyl group, is a potent analogue for PDE4 inhibition. These novel series of compounds were prepared via a 3-component reaction in a single pot. In vitro biological activity, modeling studies and crystallography data are also reported. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.11.121
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文献信息

  • Discovery of novel 1,4-dihydropyridine-based PDE4 inhibitors
    作者:Rajamohan R. Poondra、Ratnam V. Nallamelli、Chandana Lakshmi Teja Meda、B.N.V. Srinivas、Anushka Grover、Jyotsna Muttabathula、Sreedhara R. Voleti、Balasubramanian Sridhar、Manojit Pal、Kishore V.L. Parsa
    DOI:10.1016/j.bmcl.2012.11.121
    日期:2013.2
    Substituted 1,4-dihydropyridines were discovered as a novel and potent series of phosphodiesterase 4 (PDE4) inhibitors. Structure-activity relationships within this series have been carried out and studies revealed that the dihydropyridine core, with indole moiety and 3,4-dimethoxybenzyl group, is a potent analogue for PDE4 inhibition. These novel series of compounds were prepared via a 3-component reaction in a single pot. In vitro biological activity, modeling studies and crystallography data are also reported. (C) 2012 Elsevier Ltd. All rights reserved.
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