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maresin 1 methyl ester | 1391043-18-7

中文名称
——
中文别名
——
英文名称
maresin 1 methyl ester
英文别名
methyl (4Z,7R,8E,10E,12Z,14S,16Z,19Z)-7,14-dihydroxydocosa-4,8,10,12,16,19-hexaenoate
maresin 1 methyl ester化学式
CAS
1391043-18-7
化学式
C23H34O4
mdl
——
分子量
374.521
InChiKey
DDDNMJCRKTXBRX-XLWSYKCOSA-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

物化性质

  • 沸点:
    516.5±50.0 °C(Predicted)
  • 密度:
    1.014±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.3
  • 重原子数:
    27
  • 可旋转键数:
    15
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    66.8
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    maresin 1 methyl ester 在 lithium hydroxide 、 sodium dihydrogenphosphate 作用下, 以 甲醇乙酸乙酯 为溶剂, 反应 24.0h, 以77%的产率得到(4Z,7R,8E,10E,12Z,14S,16Z,19Z)-7,14-dihydroxy-4,8,10,12,16,19-docosahexaenoic acid
    参考文献:
    名称:
    Total synthesis of the macrophage derived anti-inflammatory lipid mediator Maresin 1
    摘要:
    The total synthesis of Maresin 1, an endogenous macrophage pro-resolving lipid mediator derived from docosahexaenoic acid, has been achieved. The chiral hydroxy-group at C7 was obtained via a Jacobsen hydrolytic kinetic resolution of a terminal epoxide whereas the center at C14 arises from a chiral pool strategy starting from 2-deoxy-D-ribose. Pd-0/Cu-1 Sonogashira coupling of the two key fragments and 2n(Cu/Ag) reduction completed the total synthesis of Maresin 1. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2012.05.143
  • 作为产物:
    描述:
    methyl (4Z,7R,8E)-10-oxo-7-triethylsilyloxydeca-4,8-dienoate哌啶 、 chromium dichloride 、 copper(l) iodide四(三苯基膦)钯 、 copper/silver activated zinc 、 4-甲基苯磺酸吡啶 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 16.0h, 生成 maresin 1 methyl ester
    参考文献:
    名称:
    Total synthesis of the macrophage derived anti-inflammatory lipid mediator Maresin 1
    摘要:
    The total synthesis of Maresin 1, an endogenous macrophage pro-resolving lipid mediator derived from docosahexaenoic acid, has been achieved. The chiral hydroxy-group at C7 was obtained via a Jacobsen hydrolytic kinetic resolution of a terminal epoxide whereas the center at C14 arises from a chiral pool strategy starting from 2-deoxy-D-ribose. Pd-0/Cu-1 Sonogashira coupling of the two key fragments and 2n(Cu/Ag) reduction completed the total synthesis of Maresin 1. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2012.05.143
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文献信息

  • 14-HYDROXY-DOCOSAHEXAENOIC ACID COMPOUNDS
    申请人:The Brigham And Women's Hospital, Inc.
    公开号:US20170283388A1
    公开(公告)日:2017-10-05
    The invention describes novel 14-hydroxy docosahexaenoic acid (DHA) analogues, their preparation, isolation, identification, purification and uses thereof.
  • US9611239B2
    申请人:——
    公开号:US9611239B2
    公开(公告)日:2017-04-04
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