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| 1217441-52-5

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1217441-52-5
化学式
C18H22BrO7P
mdl
——
分子量
461.246
InChiKey
PUOXRUBQFSCONZ-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

物化性质

  • 沸点:
    577.9±50.0 °C(predicted)
  • 密度:
    1.431±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.13
  • 重原子数:
    27.0
  • 可旋转键数:
    10.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    88.13
  • 氢给体数:
    0.0
  • 氢受体数:
    7.0

反应信息

  • 作为反应物:
    描述:
    、 formamide 在 diphosphorus pentasulfide 作用下, 以 四氢呋喃 为溶剂, 生成 allyl 4-[(diethoxyphosphoryl)methoxy]-8H-indeno[1,2-d][1,3]thiazole-7-carboxylate
    参考文献:
    名称:
    Structure-based drug design of tricyclic 8H-indeno[1,2-d][1,3]thiazoles as potent FBPase inhibitors
    摘要:
    With the goal of improving metabolic stability and further enhancing FBPase inhibitory activity, a series of tricyclic 8H-indeno[1,2-d][1,3]thiazoles was designed and synthesized with the aid of structure-based drug design. Extensive SAR studies led to the discovery of 19a with an IC50 value of 1 nM against human FBPase. X-ray crystallographic studies revealed that high affinity of 19a was due to the hydrophobic interaction arising from better shape complementarity and to the hydrogen bonding network involving the side chain on the tricyclic scaffold. (c) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.12.056
  • 作为产物:
    描述:
    allyl 7-[(diethoxyphosphoryl)methoxy]-1-oxoindane-4-carboxylatecopper(ll) bromide 作用下, 以 乙醇 为溶剂, 反应 2.0h, 生成
    参考文献:
    名称:
    Discovery of potent and orally active tricyclic-based FBPase inhibitors
    摘要:
    With the aim of exploring the effect of tricyclic-based FBPase inhibitors in cells and in vivo, a series of prodrugs of tricyclic phosphonates was designed and synthesized. Introducing prodrug moieties into tricyclic-based phosphonates led to the discovery of prodrug 15c, which strongly inhibited glucose production in monkey hepatocytes. Furthermore, prodrug 15c lowered blood glucose levels in fasted cynomolgus monkeys. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2010.05.041
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