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4-methoxy-2-oxa-tricyclo[13.2.2.13,7]icosa-1(18),3(20),4,6,15(19),16-hexaen-12-ol | 1354834-27-7

中文名称
——
中文别名
——
英文名称
4-methoxy-2-oxa-tricyclo[13.2.2.13,7]icosa-1(18),3(20),4,6,15(19),16-hexaen-12-ol
英文别名
4-Methoxy-2-oxatricyclo[13.2.2.13,7]icosa-1(17),3,5,7(20),15,18-hexaen-12-ol;4-methoxy-2-oxatricyclo[13.2.2.13,7]icosa-1(17),3,5,7(20),15,18-hexaen-12-ol
4-methoxy-2-oxa-tricyclo[13.2.2.13,7]icosa-1(18),3(20),4,6,15(19),16-hexaen-12-ol化学式
CAS
1354834-27-7
化学式
C20H24O3
mdl
——
分子量
312.409
InChiKey
QLKCMOKBCQLACF-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):
    4.7
  • 重原子数:
    23
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    38.7
  • 氢给体数:
    1
  • 氢受体数:
    3

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

  • 作为产物:
    描述:
    4-甲氧基-2-氧杂三环[13.2.2.13,7]二十碳-1(18),3(20),4,6,15(19),16-六烯-12-酮 在 sodium tetrahydroborate 作用下, 以 甲醇 为溶剂, 反应 0.5h, 以50%的产率得到4-methoxy-2-oxa-tricyclo[13.2.2.13,7]icosa-1(18),3(20),4,6,15(19),16-hexaen-12-ol
    参考文献:
    名称:
    Synthesis and evaluation of macrocyclic diarylether heptanoid natural products and their analogs
    摘要:
    The macrocyclic diarylether heptanoid (MDEH) natural products have been used in folk medicine for centuries. MDEHs are reported to exert anti-tumor properties by inhibiting the activation of NF-kappa B. Here we report the synthesis of a small MDEH library (first reported synthesis of racemic platycarynol) using a Grubbs cross metathesis/Ullmann cyclization strategy. Evaluation of the library led to the identification of MDEH 9b which sensitizes pancreatic cancer cells to gemcitabine mediated growth inhibition and apoptosis. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2011.11.025
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文献信息

  • Synthesis and evaluation of macrocyclic diarylether heptanoid natural products and their analogs
    作者:Vashti C. Bryant、G.D. Kishore Kumar、Abijah M. Nyong、Amarnath Natarajan
    DOI:10.1016/j.bmcl.2011.11.025
    日期:2012.1
    The macrocyclic diarylether heptanoid (MDEH) natural products have been used in folk medicine for centuries. MDEHs are reported to exert anti-tumor properties by inhibiting the activation of NF-kappa B. Here we report the synthesis of a small MDEH library (first reported synthesis of racemic platycarynol) using a Grubbs cross metathesis/Ullmann cyclization strategy. Evaluation of the library led to the identification of MDEH 9b which sensitizes pancreatic cancer cells to gemcitabine mediated growth inhibition and apoptosis. (C) 2011 Elsevier Ltd. All rights reserved.
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