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(2-[(4-methoxyphenoxy)methyl]-4-(methylethylidene)-5-oxo-2,3-dihydrofuryl)methyl 4-(4-[2-(4-methylphenyl)ethynyl]phenoxy)butanoate | 1151816-91-9

中文名称
——
中文别名
——
英文名称
(2-[(4-methoxyphenoxy)methyl]-4-(methylethylidene)-5-oxo-2,3-dihydrofuryl)methyl 4-(4-[2-(4-methylphenyl)ethynyl]phenoxy)butanoate
英文别名
[2-[(4-Methoxyphenoxy)methyl]-5-oxo-4-propan-2-ylideneoxolan-2-yl]methyl 4-[4-[2-(4-methylphenyl)ethynyl]phenoxy]butanoate
(2-[(4-methoxyphenoxy)methyl]-4-(methylethylidene)-5-oxo-2,3-dihydrofuryl)methyl 4-(4-[2-(4-methylphenyl)ethynyl]phenoxy)butanoate化学式
CAS
1151816-91-9
化学式
C35H36O7
mdl
——
分子量
568.667
InChiKey
ZCOIZBNUHPOIKW-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):
    7.4
  • 重原子数:
    42
  • 可旋转键数:
    14
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    80.3
  • 氢给体数:
    0
  • 氢受体数:
    7

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
  • 下游产品
    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:
    (2-[(4-methoxyphenoxy)methyl]-4-(methylethylidene)-5-oxo-2,3-dihydrofuryl)methyl 4-(4-[2-(4-methylphenyl)ethynyl]phenoxy)butanoate 在 ammonium cerium (IV) nitrate 作用下, 以 乙腈 为溶剂, 反应 0.17h, 以50%的产率得到[2-(hydroxymethyl)-4-(methylethylidene)-5-oxo-2,3-dihydrofuryl]methyl 4-(4-[2-(4-methylphenyl)ethynyl]phenoxy)butanoate
    参考文献:
    名称:
    Conformationally Constrained Analogues of Diacylglycerol (DAG). 31. Modulation of the Biological Properties of Diacylgycerol Lactones (DAG-lactones) Containing Rigid-Rod Acyl Groups Separated from the Core Lactone by Spacer Units of Different Lengths
    摘要:
    Diacylglycerol lactones built with a rigid 4-[(methylphenyl)ethynyl]phenyl rod that is separated from the exocyclic acylcarbonyl of the DAG-lactone core by a spacer unit of variable length were synthesized and studied. Binding affinities for a panel of classical and novel PKC isozymes in two different phospholipid environments, one corresponding to the plasma membrane of cells, were determined. The kinetics and site of translocation for the PKC isozymes alpha and delta upon treatment with the compounds were also studied as well as the early response of ERK phosphorylation and the late response of induction of apoptosis in the human prostatic carcinoma cell line LNCaP. Finally, the compounds were evaluated in terms of their interaction with biomimetic lipid/polydiacetylene membranes by the associated chromatic response. The different spatial disposition of the rigid structural motif on the DAG-lactones contributes to differential activity.
    DOI:
    10.1021/jm900186m
  • 作为产物:
    描述:
    5-(hydroxymethyl)-5-[(4-methoxyphenoxy)methyl]-3-(methylethylidene)-4,5-dihydrofuran-2-one 、 C19H18O34-二甲氨基吡啶双(2-氧代-3-恶唑烷基)次磷酰氯 作用下, 以 二氯甲烷 为溶剂, 反应 1.0h, 以224 mg的产率得到(2-[(4-methoxyphenoxy)methyl]-4-(methylethylidene)-5-oxo-2,3-dihydrofuryl)methyl 4-(4-[2-(4-methylphenyl)ethynyl]phenoxy)butanoate
    参考文献:
    名称:
    Conformationally Constrained Analogues of Diacylglycerol (DAG). 31. Modulation of the Biological Properties of Diacylgycerol Lactones (DAG-lactones) Containing Rigid-Rod Acyl Groups Separated from the Core Lactone by Spacer Units of Different Lengths
    摘要:
    Diacylglycerol lactones built with a rigid 4-[(methylphenyl)ethynyl]phenyl rod that is separated from the exocyclic acylcarbonyl of the DAG-lactone core by a spacer unit of variable length were synthesized and studied. Binding affinities for a panel of classical and novel PKC isozymes in two different phospholipid environments, one corresponding to the plasma membrane of cells, were determined. The kinetics and site of translocation for the PKC isozymes alpha and delta upon treatment with the compounds were also studied as well as the early response of ERK phosphorylation and the late response of induction of apoptosis in the human prostatic carcinoma cell line LNCaP. Finally, the compounds were evaluated in terms of their interaction with biomimetic lipid/polydiacetylene membranes by the associated chromatic response. The different spatial disposition of the rigid structural motif on the DAG-lactones contributes to differential activity.
    DOI:
    10.1021/jm900186m
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文献信息

  • Conformationally Constrained Analogues of Diacylglycerol (DAG). 31. Modulation of the Biological Properties of Diacylgycerol Lactones (DAG-lactones) Containing Rigid-Rod Acyl Groups Separated from the Core Lactone by Spacer Units of Different Lengths
    作者:Maria J. Comin、Gabriella Czifra、Noemi Kedei、Andrea Telek、Nancy E. Lewin、Sofiya Kolusheva、Julia F. Velasquez、Ryan Kobylarz、Raz Jelinek、Peter M. Blumberg、Victor E. Marquez
    DOI:10.1021/jm900186m
    日期:2009.5.28
    Diacylglycerol lactones built with a rigid 4-[(methylphenyl)ethynyl]phenyl rod that is separated from the exocyclic acylcarbonyl of the DAG-lactone core by a spacer unit of variable length were synthesized and studied. Binding affinities for a panel of classical and novel PKC isozymes in two different phospholipid environments, one corresponding to the plasma membrane of cells, were determined. The kinetics and site of translocation for the PKC isozymes alpha and delta upon treatment with the compounds were also studied as well as the early response of ERK phosphorylation and the late response of induction of apoptosis in the human prostatic carcinoma cell line LNCaP. Finally, the compounds were evaluated in terms of their interaction with biomimetic lipid/polydiacetylene membranes by the associated chromatic response. The different spatial disposition of the rigid structural motif on the DAG-lactones contributes to differential activity.
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