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hexadecyl uridin-5'-yl 2-([3R,4R]-3,4-dihydroxypyrrolidin-1-yl)ethylphosphonate | 1344121-83-0

中文名称
——
中文别名
——
英文名称
hexadecyl uridin-5'-yl 2-([3R,4R]-3,4-dihydroxypyrrolidin-1-yl)ethylphosphonate
英文别名
hexadecyl uridin-5'-yl 2-([3R,4R]-3,4-dihydroxypyrrolidin-1-N-yl)ethylphosphonate;1-[(2R,3R,4S,5R)-5-[[2-[(3R,4R)-3,4-dihydroxypyrrolidin-1-yl]ethyl-hexadecoxyphosphoryl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]pyrimidine-2,4-dione
hexadecyl uridin-5'-yl 2-([3R,4R]-3,4-dihydroxypyrrolidin-1-yl)ethylphosphonate化学式
CAS
1344121-83-0
化学式
C31H56N3O10P
mdl
——
分子量
661.773
InChiKey
CHGPVDHKMDQDQY-QBVQLYRISA-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):
    3.7
  • 重原子数:
    45
  • 可旋转键数:
    23
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.87
  • 拓扑面积:
    178
  • 氢给体数:
    5
  • 氢受体数:
    11

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:
    ((3aR,4R,6R,6aR)-6-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methyl hexadecyl (2-((3R,4R)-3,4-dihydroxypyrrolidin-1-yl)ethyl)phosphonate 在 盐酸 作用下, 以 甲醇 为溶剂, 反应 4.0h, 以590 mg的产率得到hexadecyl uridin-5'-yl 2-([3R,4R]-3,4-dihydroxypyrrolidin-1-yl)ethylphosphonate
    参考文献:
    名称:
    Lipophosphonoxins: New Modular Molecular Structures with Significant Antibacterial Properties
    摘要:
    Novel compounds termed lipophosphonoxins were prepared using a simple and efficient synthetic approach. The general structure of lipophosphonoxins consists of four modules: (i) a nucleoside module, (ii) an iminosugar module, (iii) a hydrophobic module (lipophilic alkyl chain), and (iv) a phosphonate linker module that holds together modules i-iii. Lipophosphonoxins displayed significant antibacterial properties against a panel of Gram-positive species, including multiresistant strains. The minimum inhibitory concentration (MIC) values of the best inhibitors were in the 1-12 mu g/mL range, while their cytotoxic concentrations against human cell lines were significantly above this range. The modular nature of this artificial scaffold offers a large number of possibilities for further modifications/exploitation of these compounds.
    DOI:
    10.1021/jm2009343
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文献信息

  • Lipophosphonoxins, method of their preparation and use
    申请人:Ustav organicke chemie a biochemie AV CR, v.v.i.
    公开号:EP2527351B1
    公开(公告)日:2013-12-11
  • Lipophosphonoxins: New Modular Molecular Structures with Significant Antibacterial Properties
    作者:Dominik Rejman、Alžbeta Rabatinová、António R. Pombinho、Soňa Kovačková、Radek Pohl、Eva Zbornı́ková、Milan Kolář、Kateřina Bogdanová、Otakar Nyč、Hana Šanderová、Tomáš Látal、Petr Bartůněk、Libor Krásný
    DOI:10.1021/jm2009343
    日期:2011.11.24
    Novel compounds termed lipophosphonoxins were prepared using a simple and efficient synthetic approach. The general structure of lipophosphonoxins consists of four modules: (i) a nucleoside module, (ii) an iminosugar module, (iii) a hydrophobic module (lipophilic alkyl chain), and (iv) a phosphonate linker module that holds together modules i-iii. Lipophosphonoxins displayed significant antibacterial properties against a panel of Gram-positive species, including multiresistant strains. The minimum inhibitory concentration (MIC) values of the best inhibitors were in the 1-12 mu g/mL range, while their cytotoxic concentrations against human cell lines were significantly above this range. The modular nature of this artificial scaffold offers a large number of possibilities for further modifications/exploitation of these compounds.
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