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1-十六烷醇,16-甲氧基- | 138060-30-7

中文名称
1-十六烷醇,16-甲氧基-
中文别名
——
英文名称
16-methoxyhexadecanol
英文别名
16-Methoxyhexadecan-1-ol
1-十六烷醇,16-甲氧基-化学式
CAS
138060-30-7
化学式
C17H36O2
mdl
——
分子量
272.472
InChiKey
JLPANRFWARWIGR-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):
    6.2
  • 重原子数:
    19
  • 可旋转键数:
    16
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    1-十六烷醇,16-甲氧基-四氢呋喃乙腈 为溶剂, 反应 36.0h, 生成
    参考文献:
    名称:
    4-Substituted 2-alkoxytetrahydrofurans as potent and long-lasting PAF antagonists
    摘要:
    A series of 4-substituted 2-alkoxytetrahydrofuran derivatives featuring an acetal group were prepared and evaluated for PAF antagonist activity in the PAF-induced in vitro platelet-aggregation and in vivo hypotension tests. Compound 2-[[N-acetyl-N-[[[2-(octadecyloxy)tetrahydrofuran-4-yl]methoxy]carbonyl]amino]methyl]1-ethylpyridinium chloride (4e, UR-11353) was selected for further development on the basis of its high activity and long-lasting action. The compound maintained a significant activity even 24 h after administration of a single dose of 1 mg/kg iv in the PAF-induced mortality test in mice and 10 h after administration of the same dose in the PAF-induced hypotension test in rats. Comparison with previously reported carba analogues suggests that the presence of the acetal group is the structural characteristic that confers its long-lasting activity.
    DOI:
    10.1021/jm00082a007
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文献信息

  • Modified Oligonucleotides for Telomerase Inhibition
    申请人:GERON CORPORATION
    公开号:US20150322437A1
    公开(公告)日:2015-11-12
    Compounds comprising an oligonucleotide moiety covalently linked to a lipid moiety are disclosed. The oligonucleotide moiety comprises a sequence that is complementary to the RNA component of human telomerase. The compounds inhibit telomerase activity in cells with a high potency and have superior cellular uptake characteristics.
  • MODIFIED OLIGONUCLEOTIDES FOR TELOMERASE INHIBITION
    申请人:Geron Corporation
    公开号:US20170130225A1
    公开(公告)日:2017-05-11
    Compounds comprising an oligonucleotide moiety covalently linked to a lipid moiety are disclosed. The oligonucleotide moiety comprises a sequence that is complementary to the RNA component of human telomerase. The compounds inhibit telomerase activity in cells with a high potency and have superior cellular uptake characteristics.
  • US9388415B2
    申请人:——
    公开号:US9388415B2
    公开(公告)日:2016-07-12
  • US9388416B2
    申请人:——
    公开号:US9388416B2
    公开(公告)日:2016-07-12
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